Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Probes for myctophid fish and a method for developing the same

a technology of myctophid fish and probes, which is applied in the field of molecular cloning and characterization of specific gene region sequences, can solve the problems of incompetence of methods to identify closely allied species, populations and life history stages, and the systematics of unjustified specimens are left unjustified

Inactive Publication Date: 2005-06-23
COUNCIL OF SCI & IND RES
View PDF1 Cites 2 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

The methods are incompetent to identify the closely allied species, populations and the life history stages.
This is the major bottleneck for the proper identification, population dynamics and stock assessment of these fishes leaving their systematics unjustified.
In the first place, the fish are particularly fragile and easily damaged in collecting nets, so most specimens collected tend to be in poor condition.
The problems have been compounded since specimens of many forms have not been numerous.
It is difficult to collect ample material for the taxonomic studies using the existing conventional methods.
The midwater habitat of the fish make them a uncommon and difficult material to get for work as special gears are required on board of ship.
However, very little information pertains to the families of lantern fishes.
However, in the recent years, the molecular techniques using DNAs as the genetic markers have almost replaced these traditional methods with many shortcomings and providing information about only 1% of the genome.
There is absolutely no literature available on genetic assessment of stocks from the other oceans.
No patent is available on fish DNA probes and sequences as genetic markers particularly in the myctophid fish.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Examples

Experimental program
Comparison scheme
Effect test

example 1

Chemicals, Reagents, Apparatus Used and Their Sources

[0145]

LIST OF CHEMICALSNameCompanyCatalogue Number8-HydroxyquinolineHIMEDIARM1061Acrylamide 3XcrystSRL0144139free from DNase, RNase,ProteaseAgar powderHIMEDIARM 026AgaroseSRL014011AgaroseHIMEDIARM 187BenzimidazoleSRL024727(1,3Benzodiazole)ExtrapureBromophenol blueBDH20015Buffer TabletsQUALIGENS17301pH 7.0Butan-1-olGLAXO12045A.RChloroform A.RS.D.FINE20077CHEMChloroform for HPLCSRL0322123E.D.T.A. Disodium saltHIMEDIARM 1195(Hydroxy Methyl)free from DNase, RNase,proteaseEDTAHIMEDIARM 678EDTA Disodium saltS.D.FINE38025L.RCHEMEthanolMERCKUN 1170Ethanol (Absolute)FARCO971109CHEMICALSEthidium BromideHIMEDIARM 813Hydrochloric acidIsoamyl alcoholMERCK8.18969For synthesisMagnesium ChlorideHIMEDIARM 728A.RMethanolSRL132977Extrapure A.RN,N-Dimethyl FormamideSRL042825PhenolRANBAXYP0130A.RPotassium AcetateHIMEDIARM 1091Potassium ChlorideMERCK17533PurifiedPotassium DihydrogenHIMEDIARM 249Orthophosphate A.RPropan-2-olQUALIGENS73827A.RSodium Acet...

example 2

[0161] The DNA preparation and quality & quantity of Tarletonbenia crenularis was done as given in example 1.

example 3

[0162] The DNA preparation and quality & quantity of Protomyctophum crockeri was done as given in example 2.

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
depthaaaaaaaaaa
depthaaaaaaaaaa
depthaaaaaaaaaa
Login to View More

Abstract

The DNA probes produced by molecular cloning and the characterization of specific gene region sequences is provided, these can be used as genetic markers for the genes such as Cytochrome b (cyt b); Mitochondrial control region (D-Loop); Inter Transcribed Spacers (ITS2) and Rhodopsin (ROD), 12S rRNA and 16S rRNA in mesopelagic lantern fishes which are found in the mesopelagic zones of the oceans where the photic regime is of dim light and associate themselves with the oxygen minimum layer, it also includes the recombinant DNA techniques for the preparation of specific gene probes and sequences of species specific primers of lantern fishes, novel gene probes and novel oligonucleotides for amplification of myctophid genes are disclosed.

Description

CROSS REFERENCE TO RELATED PATENT APPLICATION [0001] This application is a Divisional application of Ser. No. 09 / 782,604, filed Feb. 14, 2001. The entire specification of the aforementioned application is incorporated herein by reference.FIELD OF INVENTION [0002] This invention relates to the molecular cloning and characterization of specific gene region sequences. More particularly the invention relates to genetic markers which have been identified in several genes such as Cytochrome b (cyt b); Mitochondrial control region (D-Loop); Inter Transcribed Spacers (ITS2) and Rhodopsin (ROD) in a mesopelagic lantern fish which are found in the mesopelagic zones and associate themselves with the oxygen minimum layer. The invention is also concerned with the recombinant DNA techniques for the preparation of specific gene probes useful for identification of larval and adult life history stages of myctophids i.e. Lantern fishes. The invention also deals with construction of species specific p...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(United States)
IPC IPC(8): A01K61/00C12P19/34C12Q1/68G01N33/48G01N33/50G06F19/00
CPCC12Q1/6876
Inventor GOSWAMI, USHABERNARDI, GIACOMOGOSWAMI, SUBHASHJOHNSON, ROBERT
Owner COUNCIL OF SCI & IND RES
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products