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首页 > 产品中心 > 抗体系列 > 一抗

货号:BSCY0377

Albumin Rabbit mAb

ALB;GIG20;GIG42;Serum albumin

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别名 ALB;GIG20;GIG42;Serum albumin
基因名称 ALB
蛋白名称 ALB(Albumin)
推荐应用
反应物种 Human,Mouse,Rat,
存储缓冲液 PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
Human Gene Link 213
Human Swissprot No. P02768
Mouse Swissprot No. P07724
Rat Swissprot No. P02770
特异性 endogenous
稀释度 IHC 1:500-1:2000;WB 1:1000-1:5000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
参考分子量 MW(Observed):69kD
预测分子量 MW(Calculated):69kD
运输及保存条件 -15°C to -25°C/1 year(Do not lower than -25°C)
宿主 Rabbit
同种型 IgG,Kappa
背景介绍 This gene encodes the most abundant protein in human blood. This protein functions in the regulation of blood plasma colloid osmotic pressure and acts as a carrier protein for a wide range of endogenous molecules including hormones, fatty acids, and metabolites, as well as exogenous drugs. Additionally, this protein exhibits an esterase-like activity with broad substrate specificity. The encoded preproprotein is proteolytically processed to generate the mature protein. A peptide derived from this protein, EPI-X4, is an endogenous inhibitor of the CXCR4 chemokine receptor. [provided by RefSeq, Jul 2016],
细胞定位 Secreted
功能 Caution:A peptide arising from positions 166 to 174 was originally (PubMed:3087352 and PubMed:2437111) termed neurotensin-related peptide (NRP) or kinetensin and was thought to regulates fat digestion, lipid absorption, and blood flow.,disease:A variant structure of albumin could lead to increased binding of zinc resulting in an asymptomatic augmentation of zinc concentration in the blood [MIM:194470].,disease:Defects in ALB are a cause of familial dysalbuminemic hyperthyroxinemia (FDH) [MIM:103600]. FDH is a form of euthyroid hyperthyroxinemia that is due to increased affinity of ALB for T(4). It is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasian population.,Function:Serum albumin, the main protein of plasma, has a good binding capacity for water, Ca(2+), Na(+), K(+), fatty acids, hormones, bilirubin and drugs. Its main function is the regulation of the colloidal osmotic pressure of blood.,miscellaneous:Acetylated on Lys-223 by acetylsalicylic acid.,online information:Serum albumin entry,polymorphism:The sequence shown is that of variant albumin A.,PTM:Glycated in diabetic patients.,PTM:Kenitra variant is partially O-glycosylated at Thr-620. It has two new disulfide bonds Cys-600 to Cys-602 and Cys-601 to Cys-606.,similarity:Belongs to the ALB/AFP/VDB family.,similarity:Contains 3 albumin domains.,tissue specificity:Plasma.,
纯化 Protein A
Clonality Monoclonal
修饰类型 Unmodified
细胞定位 Secreted
组织表达 Plasma.
研究领域 >>Thyroid hormone synthesis

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