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31 results about "Silver Staining Method" patented technology

Silver Staining or GMS staining is a technique for demonstrating fungi in tissue sections. It is primarily based on staining the polysaccharides in fungal cell wall (From BioGenex).

Molecular identification method for siniperca chuatsi and siniperca scherzeri and kit

The invention discloses a method for molecular identification of Siniperca chuatsi basilewsky and Siniperca scherzeri Steindachner and a kit used by the same. The method for molecular identification comprises the following steps: DNA extraction, DNA fragment amplification, electrophoresis of PCR products and identification by a silver-staining method. The kit contains a pair of SSR primers and a standard map. The method for molecular identification can improve the efficiency and accuracy of identification of Siniperca chuatsi basilewsky and Siniperca scherzeri Steindachner, and is expected to solve the identification problem in the aquiculture of Siniperca chuatsi basilewsky and Siniperca scherzeri Steindachner and stimulate the sound development of Siniperca chuatsi culture industry.
Owner:CHANGSHA UNIVERSITY

Kaomas brilliant blue dyeing method and its special gel fixation liquid and dyeing agent

The invention discloses a Coomassie brilliant blue dyeing method and its special gel stationary liquid and coloring agent. It includes the following steps: putting SDS-PAGE glue into the gel stationary liquid for 0.5-2.0h at normal temperature; adding the glue in acetate solution with 0.5-3.0% volume percent concentration to extend for 1.0-3.0h at normal temperature; adding it to the Coomassie brilliant blue coloring agent to dye for 8-24h at normal temperature; add it to decolorizing solution I to decolorize for 1-3h; then adding to decolorizing solution II to decolorize to clear. The invention can detect SDS-PAGE glue protein at nanogram.
Owner:INST OF BOTANY CHINESE ACAD OF SCI

Silver staining method of polyacrylamide gel

The invention discloses a silver staining method of a polyacrylamide gel, which comprises the following steps of: firstly, putting an electrophoresed gel into a ceramic disc filled with distilled water; secondly, rinsing the gel by using the distilled water for two times; thirdly, adding a staining solution to carry out the solver staining; fourthly, re-rinsing the gel by using the distilled water for two times; fifthly, adding a developing solution to develop; and finally, using a digital camera to take pictures for the gel. By simplifying the silver staining steps, the silver staining method reduces the types of prepared solutions, simplifies a developing process, saves the dosage of a reagent decreasing the cost, and greatly shortens the developing time and improves the dye staining efficiency on the promise of guaranteeing obtaining an ideal target stripe. The obtained target section is clear enough for convenient genetype judgment and is particularly suitable to be used in processes of studying molecular markers and drawing genetic maps.
Owner:YANGTZE RIVER FISHERIES RES INST CHINESE ACAD OF FISHERY SCI

Ultra-rapid silver dye detecting method of sugarcane molecular marker PAGE gel

The invention discloses an ultra-fast silver staining test method of cane molecule tagged PAGE gel, which comprises the following steps: a modified polyacrylamide gel with the concentration of 5 percent is used for the electrophoresis detection of SSR and AFLP tagged PCR amplified primer; the gel after the electrophoresis is placed into a dyeing liquid to be dyed; the gel is taken out from the dyeing liquid, quickly rinsed, and placed into a developing solution to be developed; the developed gel is cleaned by distilled water for two times and dried, and tape reading is implemented; the ultra-fast silver staining test method combines four traditional steps of fixing, dyeing, developing and image fixing into two simplest steps, thus simultaneously reducing rinsing frequency and time, reducing the use of a fixing liquid, an image fixing liquid, acetic acid, absolute ethyl alcohol, sodium carbonate and sodium hyposulfite, not only greatly decreasing silver staining time and reagent cost, but also ensuring high-quality silver staining effect, and compared with other traditional or improved isotopic silver staining methods, the ultra-fast silver staining test method has larger time and cost advantages.
Owner:SUGARCANE RES INST OF YUNNAN ACADEMY OF AGRI SCI

Molecular identification method for siniperca kneri garman and siniperca scherzeri and kit

The invention discloses a method for molecular identification of Siniperca kneri and Siniperca scherzeri Steindachner and a kit used by the same. The method for molecular identification comprises the following steps: DNA extraction, DNA fragment amplification, electrophoresis of PCR products and identification by a silver-staining method. The kit contains a pair of SSR primers and a standard map. The method for molecular identification can improve the efficiency and accuracy of identification of Siniperca kneri and Siniperca scherzeri Steindachner, and is expected to solve the identification problem in the aquiculture of Siniperca kneri and Siniperca scherzeri Steindachner and stimulate the sound development of Siniperca chuatsi culture industry.
Owner:CHANGSHA UNIVERSITY

Rapid neuron staining method based on Golgi silver staining method

The invention discloses a rapid neuron staining method based on a Golgi silver staining method. The rapid neuron staining method based on the Golgi silver staining method is characterized in that according to mass volume ratio concentration, the aqueous solution with 5 % of potassium dichromate, the aqueous solution with 5 % of mercuric chloride and the aqueous solution with 5 % of potassium chromate are prepared into a Golgi silver staining solution in the volume ratio of 1:1:1, a brain tissue is soaked in the silver staining solution at 37 DEGCfor 36-48 hours, the soaked brain tissue is sliced on a vibrating slicer, tissue sections are arranged on a glass slide coated with gelatin, the tissue sections stay overnight, then conventional ammonia developing is conducted, gradient alcohol dehydration is conducted, the transparency process is conducted by xylene, finally, the tissue sections are sealed by netrual gum, and the tissue sections are observed through a microscope. According to the rapid neuron staining method based on the Golgi silver staining method, staining can be conducted on each encephalic region of the brain, the staining result is clear, details are obvious, and research staff can observe the neuron structure of the brain tissues conveniently, the convenient and fast means is provided for case analysis of nervous system lesions, and the rapid neuron staining method based on the Golgi silver staining method has significant meanings for the field of foundational research of neurology.
Owner:HEFEI UNIV OF TECH

DNA silver staining method

The invention discloses a DNA silver staining method. The method comprises the following steps: (1) cutting off power supply after finishing electrophoresis, pouring a buffer solution out from an electrophoresis tank, then taking off a gel plate, putting the rubber plate into a porcelain dish filled with distilled water, and rinsing the gel plate by the distilled water for 2 to 3 times; (2) carrying out silver staining: adding a staining agent to carry out silver staining, shaking ceaselessly, staining for 8 to 12 minutes, and then rinsing by the distilled water for 2 to 3 times; (3) carrying out developing: adding a developing agent to carry out color development, shaking ceaselessly, and developing for 8 to 12 min; (4) rinsing by the distilled water for 2 to 3 times; and (5) carrying out gel shooting: spreading gelatin onto a X-ray film viewer to take a photo. The method integrates the fixing step and the staining step, adopts ethanol to fix, and overcomes the defects that the belt color is lighter when acetic acid is used for fixing, and the acetic acid has penetrating odor, causticity and so on in the prior sliver staining method. Additionally, the method does not need use ethanol and / or acetic acid to stop developing color, omits the color development stopping step, and solves the problems of penetrating odor and causticity brought by the acetic acid and the like.
Owner:HENAN UNIV OF SCI & TECH

Analytical method for beta-amyloid protein pathology by using thioflavine T staining

InactiveCN103278626AClear etiologyStrong impetusFluorescence/phosphorescencePharmacological interventionsDisease patient
The invention relates to an analytical method for beta-amyloid protein pathology by using thioflavine T staining. The method comprises the following processes: A, a patient pathological specimen source, B, an experimental animal pathological specimen source, C, treatment of patient and experimental animal brain tissue specimens, D, immumohistochemical staining of specimen beta-amyloid protein 1-42, E, thioflavine T staining of the specimen, and F, optical / fluorescence microscope pathological examination. The method has the advantages of introducing and widely using the thioflavine T to mark an amyloid protein disease patient brain tissue pathological specimen and assess the pharmacological intervention effect of alzheimer disease (AD) transgenic animals; compared with the traditional silver staining method and A beta immunohistochemical method, the method provided by the invention has the characteristics of being simple and feasible, and sensitive and reliable, is beneficial for clearing the nosetiology of cerebral hemorrhage, and has great guide value on formulation of patient secondary intervening measures. The wide application of the technology has a powerful promoting effect on clinical pathological research and translational medicine research of the A beta related diseases (alzheimer disease and amyloid angiopathy).
Owner:徐俊

DNA silver staining method in polyacrylamide gel electrophoresis

The invention discloses a DNA silver staining method in polyacrylamide gel (PAGE) electrophoresis, which comprises the steps of soaking polyacrylamide gel with 0.1% AgNO3 for 10-15min, washing with distilled water twice, developing with 0.04% Na2CO3, 2mL of 37% HCOH / L and 2% mixed solution for 5-6min, and flushing twice with distilled water to complete the whole dyeing process. The conventional DNA silver staining method needs 5-6 chemical reagents, prepares 4 solutions and spends 40-60min to complete the dyeing step, but the method only needs 4 chemical reagents, prepares 2 solutions and spends 20min to reach the result the same as that of the conventional dyeing method, and in denaturing polyacrylamide electrophoresis (PAGE), the dyeing method can reduce the amount of DNA to 0.44ng; and in non-denaturing polyacrylamide electrophoresis (PAGE), the amount of DNA can be reduced to 3.5ng. Compared with the conventional dyeing method, the method of the invention saves the time, reduces the cost, and increases the detection sensitivity.
Owner:NORTHWEST A & F UNIV

Silver dyeing method

The invention relates to a sliver staining method, including: adding gel into staining solution for 5-10 min, the said staining solution containing 20-75v% ethanol,0.5-3v% nitric acid,0.05-0.8wt% silver nitrate, then rinsing silver stained gel for 1-5 min using deionized water, revealing to clear streak using coloring solution, the said coloring solution containing 0.1-0.3v% formaldehyde,2-4wt%Na#-[2]CO#-[3], at last terminating revealing using 10v% acetic acid aqueous solution for 0.5-3 min. The advantages of silver staining method provided by the invention lie in : integrating fixative solution, oxidation solution and revealing solution into one solution thus reducing the reagent volume, simplifying the steps to three. The silver staining time is less than 20 minutes, which promotes the silver staining efficiency, and havs no influence the silver staining sensitivity.
Owner:CHINA AGRI UNIV

Functional marker for wheat phytoene synthase gene psy-e2 and application thereof

The invention discloses a functional marker for wheat phytoene synthase gene psy-e2, wherein PCR (Polymerase Chain Reaction) primer sequences are PSY-F and PSY-R. The assay steps are as follows: a Buffer S method is adopted to extract the whole genome DNA of wheat leaves; the psy-e2 gene functional marker is utilized to assay the extracted DNA to carry out PCR amplification; a PCR product undergoes PAGE (polyacrylamide gel electrophoresis), and after a silver staining method is adopted to carry out chromogenic reaction, a result is observed. The functional molecular marker for psy-e2 in the invention does not depend on molecular genetic mapping, and the functional marker can be utilized to increase the efficiency of molecular marker-assisted selection, and can also be directly applied in production practice, providing a technical support for the breeding of improved lines or hybrids with low flavin content by the molecular marker-assisted selection method.
Owner:SHANDONG AGRICULTURAL UNIVERSITY

Optimized rice indica and japonica performance detection system and optimized rice indica and japonica performance detection method

InactiveCN106399502AStrong specificityThe detection belt type is clear and obviousMicrobiological testing/measurementElectrophoresisImage detection
The invention discloses an optimized rice indica and japonica performance detection system. The optimized rice indica and japonica performance detection system comprises a molecular marker system, an amplification system, an electrophoresis system and a gel imaging system, wherein the molecular marker system is used for molecular marking of a group of indica and japonica high in specificity, the amplification system is used for PCR (polymerase chain reaction) amplification, the electrophoresis system is used for PAGE (polyacrylamide gel electrophoresis), and the gel imaging system is used for imaging detection of banding patterns. The optimized rice indica and japonica performance detection system has the advantages that the detected banding patterns are clear and obvious, and adopting a GoldView aqueous solution for staining substitutes for a traditional PAGE gel silver staining method, so that an operation process is simpler and more convenient, and the amplification efficiency and the detection efficiency are both improved. The invention further provides a rice indica and japonica performance differentiating method. A designed indica and japonica performance differentiating marker is high in specificity, only one indica or japonica specific band pattern occurs, and the occurrence frequency of the specific band pattern in an indica and japonica group is above 70.0%. The indica and japonica performance is measured through the indica and japonica degree, and accordingly comparison results are more objective and comprehensive.
Owner:RICE RES INST GUANGDONG ACADEMY OF AGRI SCI

Yunnan-type hybridrice restoring line molecular auxiliary selecting method

The present invention relates to a method for molecular auxiliary selection of Dian-type hybrid rice restoring line, belonging to the field of breeding technology. Said method includes the following steps: sowing and transplanting the material to be identified, after the material is transplanted for 15-40 days, taking leaf, extracting total DNA of rice; determining sample DNA concentration and quantitatively diluting DNA to 25 ng / ul; then using micro-satellite marker OSR33 and RM228 which are positioned in tenth chromosome of rice and tightly linked with Dian-type restoring gene as primer, making PCR reaction; making poly-acrylamide gel electrophoresis, utilizing silver staining method to detect PCR product and electrophoresis result; then judging that the tested material has restoring gene or not and can be used as restoring line of Dian-type hybrid rice or not. Said invention can quickly and effectively screen restoring line of Dian-type hybrid rice.
Owner:YUNNAN AGRICULTURAL UNIVERSITY

High-efficiency silver staining method for PAGE

The invention belongs to the field of molecular genetics and in particular relates to a high-efficiency silver staining method suitable for polyacrylamide gel. The method comprises the following steps: (1) soaking taken gel in stationary liquid, and treating for 2 minutes, wherein the stationary liquid comprises 10 percent Ethanol and 1.0 percent Acetic acid according to a formula; (2) adding the treated gel into 0.2 percent AgNO3 penetrating fluid for treating for 3 minutes, rapidly adding the gel into water, and cleaning for 20 seconds; and (3) adding the gel into a developing solution, and developing within 2 minutes, wherein the developing solution comprises 2 percent NaOH, 20ml of 37 percent HCOH / L and 0.00175 percent Na2S2O3 according to a formula. According to the method disclosed by the invention, the silver staining process can be finished within 10 minutes, the time consumption is almost the lowest in reported silver staining methods, and the experimental efficiency is obviously improved.
Owner:INST OF COTTON RES CHINESE ACAD OF AGRI SCI

Fast silver staining method for RCA (rolling circle amplification) product

The invention belongs to the fields of biochemistry, molecular biology and detection methods of nucleic acid amplification, and discloses a fast silver staining method for gel fixed at the bottom of atube for RCA visual detection. In the method, the gel containing an RCA product to be detected is fixedly arranged at the bottom of the tube, and a reagent required by silver staining is directly added into and removed from the tube to perform silver staining on the gel at the bottom of the tube to further implement semi-quantitative or qualitative analysis over an RCA sample in the gel. According to the method, a fast, convenient and visual detection technology is provided for an RCA-based detection technology, and the method has practical value and broad application prospect.
Owner:中国医科大学

Method for growing DNA at 3'-OH terminal of RNA based on terminal deoxyribonucleotide transferase (TdT) and free of template dependence

The invention discloses a method for growing DNA at the 3'-OH terminal of RNA based on TdT and free of template dependence. The method mainly comprises the following steps: with miRNA122 and DNA122 asprimers, adding dNTPs, 1*CoCl2, 1*RB10* and TdT to form a 20-microliter reaction system; adjusting reaction conditions including reaction time, reaction concentration, reaction raw materials and reaction substrates; verifying a RNA extension effect through polyacrylamide gel electrophoresis and a silver staining method; and verifying the difference of extension effects of DNA and RNA under the action of the TdT through a fluorescence method. The invention relates to the novel application of TdT; and a series of high-sensitivity RNA detection platforms can be established by utilizing the new application, and a new detection direction is provided for miRNAs such as tumor markers in the future.
Owner:TIANJIN UNIV

Human coagulation factor light chain protein and use of the same

In the invention, the minimum inhibitory concentrations of human coagulation factor light-chain proteins against different Gram-negative bacteria are detected with the in vitro antibacterial activity and the inhibiting effect of the human coagulation factor light-chain proteins against different Gram-negative bacteria is detected with the in vivo antibacterial activity. It has been shown that human coagulation factor light-chain proteins have an obvious inhibitory effect on the Gram-negative bacteria, so as to develop a novel class of medicaments for treating Gram-negative bacteria infection. It has been demonstrated by mass spectrometry and silver staining that human coagulation factor light-chain proteins have the effect on hydrolyzing and eliminating the endotoxin, which facilitates the development of a novel class of medicaments for treating endotoxemia. The human coagulation factor light-chain proteins are light chain proteins of human coagulation factors VII, IX, and X, as well as a protein having homology of more than 50% thereof.
Owner:CHENGDU SOURCEBIO LIMITED LIABILITY

Corn SSR (Solid-State Relay) marked rapid silver staining detection method for breeding improvement

InactiveCN108165614AWill not affect the result of readingMicrobiological testing/measurementBand patternBiology
The invention discloses a corn SSR (Solid-State Relay) marked rapid silver staining detection method for breeding improvement and relates to the technical field of corn breeding. Corn seeds are adopted, and the corn seeds are provided by 28 different breeding institutes. By using a rapid silver staining method, two steps of fixation and dyeing are integrated into one, developing can be carried outdirectly without dilution after dyeing, a clear banding pattern can be obtained within 2 minutes generally, the whole process is not longer than 10 minutes, in addition, the dyeing background is deepened for a certain extent along with time, and the reading results are not affected by long-term development.
Owner:ANHUI TIANQIN AGRI TECH CO LTD

Molecular identification method for siniperca chuatsi and siniperca scherzeri and kit

The invention discloses a method for molecular identification of Siniperca chuatsi basilewsky and Siniperca scherzeri Steindachner and a kit used by the same. The method for molecular identification comprises the following steps: DNA extraction, DNA fragment amplification, electrophoresis of PCR products and identification by a silver-staining method. The kit contains a pair of SSR primers and a standard map. The method for molecular identification can improve the efficiency and accuracy of identification of Siniperca chuatsi basilewsky and Siniperca scherzeri Steindachner, and is expected tosolve the identification problem in the aquiculture of Siniperca chuatsi basilewsky and Siniperca scherzeri Steindachner and stimulate the sound development of Siniperca chuatsi culture industry.
Owner:CHANGSHA UNIVERSITY

Kaomas brilliant blue dyeing method and its special gel fixation liquid and dyeing agent

The invention discloses a Coomassie brilliant blue dyeing method and its special gel stationary liquid and coloring agent. It includes the following steps: putting SDS-PAGE glue into the gel stationary liquid for 0.5-2.0h at normal temperature; adding the glue in acetate solution with 0.5-3.0% volume percent concentration to extend for 1.0-3.0h at normal temperature; adding it to the Coomassie brilliant blue coloring agent to dye for 8-24h at normal temperature; add it to decolorizing solution I to decolorize for 1-3h; then adding to decolorizing solution II to decolorize to clear. The invention can detect SDS-PAGE glue protein at nanogram.
Owner:INST OF BOTANY CHINESE ACAD OF SCI

An Improved Grocott Hexamine Silver Staining Method and Its Application

ActiveCN104677713BSolve the defect of easy peeling offEasy to take offPreparing sample for investigationPolypideBiochemistry
The invention discloses an improved Grocott silver hexosamine staining method and applications thereof. The staining method comprises the steps of preparing paraffin-embedded sections, staining, carrying out dehydrated hyalinizing, and carrying out section sealing, wherein in the step of preparing paraffin-embedded sections, a sliced paraffin section is adhered to a glass slide subjected to APES treatment. The method overcomes the defect that section shedding easily occurs in the process of staining, especially for frankliniella occidentalis with a small somatotype, the non-section-shedding rate is over 70%. In addition, the internal tissues of polypides in sections obtained according to the staining method disclosed by the invention are red, blastospores in polypides are black, therefore, the polypides are clearly visible, and the staining effect is excellent.
Owner:QINGDAO AGRI UNIV

A kind of kit and identification method for five kinds of mandarin fish molecules

The invention provides a kit and an identification method for molecules of five Sinipercinae fishes. The kit comprises three pairs of SSR primers and standard maps. The identification method for molecules of five Sinipercinae fishes by using the kit comprises the following steps: 1) DNA extraction: a step of acquiring the fin ray or muscle tissue of a to-be-tested Siniperca chuatsi sample, extracting genome DNA and measuring the purity and concentration of the genome DNA; 2) DNA fragment amplification: a step of amplifying the genome DNA of the to-be-tested sample by using a polymerase chain reaction; 3) electrophoresis and silver staining identification of PCR products: a step of carrying out electrophoretic separation on the PCR products by using nondenaturing polyacrylamide gel, then carrying out staining by using a conventional silver staining method and taking photos to record electrophoresis results; and 4) comparison with the standard maps. The kit and the identification method provided by the invention can substantially improve efficiency and accuracy of identification of important economic and rare varieties of Sinipercinae and are beneficial for protection of genetic resources of Sinipercinae fishes and sustained sound development of the breeding industry of Siniperca chuatsi.
Owner:HUAZHONG AGRI UNIV

Silver dyeing method

The invention relates to a sliver staining method, including: adding gel into staining solution for 5-10 min, the said staining solution containing 20-75v% ethanol,0.5-3v% nitric acid,0.05-0.8wt% silver nitrate, then rinsing silver stained gel for 1-5 min using deionized water, revealing to clear streak using coloring solution, the said coloring solution containing 0.1-0.3v% formaldehyde,2-4wt%Na#-[2]CO#-[3], at last terminating revealing using 10v% acetic acid aqueous solution for 0.5-3 min. The advantages of silver staining method provided by the invention lie in : integrating fixative solution, oxidation solution and revealing solution into one solution thus reducing the reagent volume, simplifying the steps to three. The silver staining time is less than 20 minutes, which promotes the silver staining efficiency, and havs no influence the silver staining sensitivity.
Owner:CHINA AGRI UNIV

Simple sequence repeats (SSR) primer and method for identifying purity of hybrid seeds of Yunnan raphanus sativus L. No. 2

The invention provides a simple sequence repeats (SSR) primer SSR06 for identifying the purity of hybrid seeds of Yunnan raphanus sativus L. No. 2, and further provides a method for identifying the purity of the hybrid seeds of the Yunnan raphanus sativus L. No. 2. The method comprises the following steps: Step 1, extracting genome DNA of to-be-detected samples, the hybrid seeds of the Yunnan raphanus sativus L. No. 2; Step 2, performing polymerase chain reaction (PCR) amplification by employing the SSR primer SSR06 by taking the genome DNA, extracted in the step 1, of the hybrid seeds of theYunnan raphanus sativus L. No. 2 as a template; Step 3, separating an amplification product in the step 2 by polyacrylamide gel electrophoresis, performing staining by a silver staining method, performing photographing and making statistics on results; and Step 4, calculating the purity of the hybrid seeds of the Yunnan raphanus sativus L. No. 2 by utilizing the statistical results in the step 3.The SSR primer SSR06 provided by the invention has high specificity, and accurate identification results, can quickly, accurately and conveniently identify the purity of hybrid seeds, and overcomes the shortcoming that time and vigor are consumed by using field plot planting identification to identify the purity of the hybrid seeds.
Owner:云南省农业科学院园艺作物研究所

Method for screening allelotype of immune related gene DQA1 Exon 2-(A-C) of goat

The invention discloses a method for screening the allelotype of an immune related gene DQA1 Exon 2-(A-C) of goat. A primer is designed according to the sequence of exon-2 of a DQA1 gene, the genome DNA of white goat is used as a template to carry out PCR (Polymerase Chain Reaction) amplification, purification sequencing is carried out on the PCR product, and the polymorphic site of the exon-2 of DQA1 gene is screened preliminarily; a target fragment is subjected to PCR amplification by using DNA of the white goat genome as a template, and the PCR product is treated by a denaturing agent, and the denatured amplification fragment is subjected to polyacrylamidedel gel electrophoresis detection; rubber is dyed by applying a silver staining method, and partial allelotype of the exon-2 of the DQA1 gene of white goat from Guizhou is determined according to the result of polyacrylamidedel gel electrophoresis. A convenient, quick and accurate method is provided to PCR-SSCP screening and type determining of exon-2 polymorphism of DQA1 gene of different varieties of goat, and can be used for detecting partial allele of exon2 of goat immune related DQA1 gene, so that the problem of difficult type determination on highly polymorphic genes in the existing PCR-SSCP technology can be solved.
Owner:广西平果润民脱贫发展有限公司

DNA silver staining method in polyacrylamide gel electrophoresis

The present invention discloses a DNA silver staining method in polyacrylamide gel (PAGE) electrophoresis, which comprises the steps of soaking polyacrylamide gel with 0.1% AgNO3 for 10-15min, washing with distilled water twice, developing with 0.04% Na2CO3, 2mL of 37% HCOH / L and 2% mixed solution for 5-6min, and flushing twice with distilled water to complete the whole dyeing process. The conventional DNA silver staining method needs 5-6 chemical reagents, prepares 4 solutions and spends 40-60min to complete the dyeing step, but the method only needs 4 chemical reagents, prepares 2 solutions and spends 20min to reach the result the same as that of the conventional dyeing method, and in denaturing polyacrylamide electrophoresis (PAGE), the dyeing method can reduce the amount of DNA to 0.44ng; and in non-denaturing polyacrylamide electrophoresis (PAGE), the amount of DNA can be reduced to 3.5ng. Compared with the conventional dyeing method, the method of the present invention saves the time, reduces the cost, and increases the detection sensitivity.
Owner:NORTHWEST A & F UNIV

A Rapid Silver Staining Method for RCA Amplified Products

The invention belongs to the fields of biochemistry, molecular biology and detection methods of nucleic acid amplification, and discloses a fast silver staining method for gel fixed at the bottom of atube for RCA visual detection. In the method, the gel containing an RCA product to be detected is fixedly arranged at the bottom of the tube, and a reagent required by silver staining is directly added into and removed from the tube to perform silver staining on the gel at the bottom of the tube to further implement semi-quantitative or qualitative analysis over an RCA sample in the gel. According to the method, a fast, convenient and visual detection technology is provided for an RCA-based detection technology, and the method has practical value and broad application prospect.
Owner:中国医科大学

Quantitative protein silver staining method of freshwater ciliates

The invention provides a quantitative protein silver staining method of freshwater ciliates. The method includes sample fixation, filtration and concentration, agar embedding, agar solidification, protein silver staining and dehydrating and mounting. According to the method, a staining effect is better, slices produced in unit time are more, an overall staining effect is uniform, and mounting is easy. The method is more suitable for protein silver staining technology of qualitative and quantitative study of planktonic ciliates in typical eutrophic lakes of China.
Owner:FISHERIES RES INST ANHUI ACAD OF AGRI SCI
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