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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

  • 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

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.
PubMedPubMed
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.
















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