Prediction reagent kit for early stage primary liver cancer patient postoperative metastasis and recurrence based on immune molecule
A technology of primary liver cancer and immune molecules, applied in the biological field, can solve the problems involving many indicators and difficult clinical application, and achieve simple, feasible and reliable results of gene expression level
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Embodiment 1
[0027] A kit for predicting postoperative metastasis and recurrence of patients with early primary liver cancer based on immune molecules, including interleukin 2 amplification detection reagents, internal reference gene amplification detection reagents, normal liver tissue control substances, negative control substances, positive control substances, RNase-free water;
[0028] Wherein, the interleukin 2 amplification detection reagent consists of 10mmol / L tris hydrochloride, 2.5mM magnesium chloride, 0.35pmol / ul deoxyribonucleotide triphosphate, 0.10U / Taq enzyme, 0.35pmol fluorescent label Interleukin-2 self-quenching probe and primers, 20u / ul RNase inhibitor and water;
[0029] Internal reference gene amplification detection reagent consists of 10mmol / L Tris hydrochloride, 2.5mM magnesium chloride, 0.35pmol / ul deoxyribonucleotide triphosphate, 0.10U / Taq enzyme, 0.35pmol fluorescently labeled 3-phosphoglycerol Aldehyde dehydrogenase gene self-quenching probe and primer, 20u / u...
Embodiment 2
[0039] A kit for predicting postoperative metastasis and recurrence of patients with early primary liver cancer based on immune molecules, including interleukin 2 amplification detection reagents, internal reference gene amplification detection reagents, normal liver tissue control substances, negative control substances, positive control substances, RNase-free water;
[0040] Wherein, the interleukin 2 amplification detection reagent consists of 5mmol / L Tris hydrochloride, 2.0mM magnesium chloride, 0.3pmol / ul deoxyribonucleotide triphosphate, 0.05U / Taq enzyme, 0.3pmol fluorescent label Interleukin-2 self-quenching probe and primers, 10u / ul RNase inhibitor and water;
[0041] The internal reference gene amplification detection reagent consists of 5mmol / L Tris hydrochloride, 2.0mM magnesium chloride, 0.3pmol / ul deoxyribonucleotide triphosphate, 0.05U / Taq enzyme, 0.3pmol fluorescently labeled 3-phosphoglycerol Aldehyde dehydrogenase gene self-quenching probe and primer, 10u / ul ...
Embodiment 3
[0048] A kit for predicting postoperative metastasis and recurrence of patients with early primary liver cancer based on immune molecules, including interleukin 2 amplification detection reagents, internal reference gene amplification detection reagents, normal liver tissue control substances, negative control substances, positive control substances, RNase-free water;
[0049] Wherein, the interleukin 2 amplification detection reagent consists of 15mmol / L tris hydrochloride, 3.0mM magnesium chloride, 0.4pmol / ul deoxyribonucleotide triphosphate, 0.15U / Taq enzyme, 0.4pmol fluorescent label Interleukin-2 self-quenching probe and primer, 30u / ul RNase inhibitor and water;
[0050] The internal reference gene amplification detection reagent consists of 15mmol / L Tris hydrochloride, 3.0mM magnesium chloride, 0.4pmol / ul deoxyribonucleotide triphosphate, 0.15U / Taq enzyme, 0.4pmol fluorescently labeled 3-phosphoglycerol Aldehyde dehydrogenase gene self-quenching probe and primer, 30u / ul...
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