牛血清白蛋白单克隆抗体

产品货号：

BN42017M
中文名称：

牛血清白蛋白单克隆抗体
英文名称：

Mouse anti-Bovine Serum Albumin Monoclonal antibody
品牌：

Biorigin

货号

产品规格

售价

备注
BN42017M-50ul

50ul

¥1486.00

交叉反应：Cow,Goat 推荐应用：WB
BN42017M-100ul

100ul

¥2360.00

交叉反应：Cow,Goat 推荐应用：WB

产品描述

英文名称	Bovine Serum Albumin
中文名称	牛血清白蛋白单克隆抗体
别名	ALB; Bovine Serum Albumin; Albumin; Allergen Bos d 6; BSA; Serum albumin; ALBU_BOVIN.
研究领域	细胞生物
抗体来源	Mouse
克隆类型	Monoclonal
克隆号	10D7
交叉反应	Cow, Goat,
产品应用	WB=1:500-1000 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
分子量	66kDa
细胞定位	分泌型蛋白
性状	Liquid
浓度	1mg/ml
免疫原	Purified BSA Protein:
亚型	IgG
纯化方法	affinity purified by Protein G
储存液	0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存条件	Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMed	PubMed
产品介绍	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 plasma, typically binds about 80% of all plasma zinc. 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-223 by acetylsalicylic acid. 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. Similarity: Belongs to the ALB/AFP/VDB family. Contains 3 albumin domains. SWISS: P02769 Gene ID: 280717 Database links: Entrez Gene: 280717 Cow Important Note: This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.