A3293
抗-人白蛋白 兔抗
whole antiserum
别名:
Albumin Antibody, Albumin Antibody - Anti-Human Albumin antibody produced in rabbit, Anti Human Albumin Antibody
一般描述
白蛋白′一级结构由单链氨基酸组成，二级结构由六匝的α-螺旋和17个二硫键组成。三级结构为3D，由三个域I、II和III组成。这些域中的每一个分别由子域IAB，IC，IIAB，IIC，IIIAB，IIIC组成。
免疫原
人白蛋白
应用
大鼠肝细胞在胶原蛋白包被的盖玻片上生长，固定在福尔马林中，并用甲醇透化，然后与兔抗人白蛋白抗体孵育。
抗人白蛋白抗体可用于定量沉淀试验、高通量蛋白微阵列分析和免疫细胞化学。
抗人白蛋白抗体已用于酶联免疫吸附试验（ELISA）和人血清白蛋白（HSA）抗体的固定化。
生化/生理作用
抗人白蛋白抗体对人白蛋白具有特异性。
白蛋白在血液中许多外源性和内源性物质的运输和沉积中起主要作用。
白蛋白是一种运输蛋白，可与多种配体结合，如脂肪酸、胆红素、血红素、药物、氨基酸和离子等。白蛋白也可作为锌载体蛋白，用于调节生理过程 。
外形
本产品为含有15 mM叠氮化钠（作为防腐剂）的液体。
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储存分类代码
13 - Non Combustible Solids
WGK
WGK 1
闪点(°F)
Not applicable
闪点(°C)
Not applicable
法规信息
常规特殊物品
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Chie Naito et al.
Molecular genetics and metabolism reports, 39, 101069-101069 (2024-03-22)
Glycogen Storage disease type 4 (GSD4), a rare disease caused by glycogen branching enzyme 1 (GBE1) deficiency, affects multiple organ systems including the muscles, liver, heart, and central nervous system. Here we report a GSD4 patient, who presented with severe
The analysis and characterisation of immuno-unreactive urinary albumin in healthy volunteers
Clavant S P, et al.
Clinical Biochemistry, 39(2), 143-151 (2006)
Interaction of bovine (BSA) and human (HSA) serum albumins with ionic surfactants: spectroscopy and modelling
Gelamo E L, et al.
Biochimica et Biophysica Acta, Protein Structure and Molecular Enzymology, 1594(1), 84-99 (2002)
Yi Luo et al.
The Journal of pharmacology and experimental therapeutics, 321(3), 884-891 (2007-03-21)
Epidermal growth factor (EGF) stimulation of cell cycle progression in cultured primary hepatocytes has previously been reported to be dependent on the mammalian target of rapamycin (mTOR) elements of the phosphoinositide 3-kinase (PI3K) signaling cascade and not the Akt pathway.
Holger Husi et al.
Biomedical reports, 10(3), 165-174 (2019-03-25)
Several potential urinary biomarkers exhibiting an association with upper gastrointestinal tumour growth have been previously identified, of which S100A6, S100A9, rabenosyn-5 and programmed cell death 6-interacting protein (PDCD6IP) were further validated and found to be upregulated in malignant tumours. The
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