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牛血清白蛋白單克隆抗體

產品貨號：

BN42017M
中文名稱：

牛血清白蛋白單克隆抗體
英文名稱：

Mouse anti-Bovine Serum Albumin Monoclonal antibody
品牌：

Biorigin

貨號

產品規格

售價

備注
BN42017M-50ul

50ul

￥1486.00

交叉反應：Cow,Goat 推薦應用：WB
BN42017M-100ul

100ul

￥2360.00

交叉反應：Cow,Goat 推薦應用：WB

產品描述

英文名稱	Bovine Serum Albumin
中文名稱	牛血清白蛋白單克隆抗體
別名	ALB; Bovine Serum Albumin; Albumin; Allergen Bos d 6; BSA; Serum albumin; ALBU_BOVIN.
研究領域	細胞生物
抗體來源	Mouse
克隆類型	Monoclonal
克隆號	10D7
交叉反應	Cow, Goat,
產品應用	WB=1:500-1000 not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
分子量	66kDa
細胞定位	分泌型蛋白
性狀	Liquid
濃度	1mg/ml
免疫原	Purified BSA Protein:
亞型	IgG
純化方法	affinity purified by Protein G
儲存液	0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件	Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
PubMed	PubMed
產品介紹	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.