Mouse Anti-Albumin antibody |
产品应用(已验证) |
WB |
推荐稀释比例 |
WB=1:500-1000, |
研究领域 |
细胞生物 |
标签 |
Array |
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Sample:
Lane 1: Serum (Goat) at 20 ug
Lane 2: Serum (Cow) at 20 ug
Primary: Anti-Bovine Serum Albumin (bsm-33201M) at 1/1000 dilution
Secondary: IRDye800CW Goat Anti-Mouse IgG at 1/20000 dilution
Predicted band size: 67 kD
Observed band size: 67 kD
RRID:RRID
产品名称:Mouse Anti-Albumin antibody
别名: ALB; Bovine Serum Albumin; Allergen Bos d 6; BSA; Serum albumin; ALBU_BOVIN.
中文名称:白蛋白单克隆抗体
英文名称:Mouse Anti-Albumin antibody
抗体来源: Mouse
克隆类型:单克隆
细胞定位:分泌型蛋白
性 状:Liquid
亚 型:IgG
纯化方法:affinity purified by Protein G
保存条件:Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
免 疫 原:Purified BSA Protein
SWISS:P02769
Gene ID :280717
Human Gene ID:213
Albumin is a soluble, monomeric protein which comprises about one-half of the blood serum protein. Albumin functions primarily as a carrier protein for steroids, fatty acids, and thyroid hormones and plays a role in stabilizing extracellular fluid volume. Albumin is a globular unglycosylated serum protein of molecular weight 65,000. Albumin is synthesized in the liver as preproalbumin which has an N-terminal peptide that is removed before the nascent protein is released from the rough endoplasmic reticulum. The product, proalbumin, is in turn cleaved in the Golgi vesicles to produce the secreted albumin. [provided by RefSeq, Jul 2008].
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. Major zinc transporter in pl
Subcellular Location:Secreted.
Tissue Specificity:Plasma.
Post-translational modifications: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.
Glycated in diabetic patients.
Phosphorylation sites are present in the extracelllular medium.
Acetylated on Lys-
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 hyperthyroxinemi
Similarity:Belongs to the ALB/AFP/VDB family.
Contains 3 albumin domains.
Important Note:This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.