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Transferrin Monoclonal Antibody(5A4)
Transferrin Monoclonal Antibody(5A4)
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Transferrin Monoclonal Antibody(5A4)
市场价格
经销商客户: ¥440.0
实验室客户: ¥600.0
近期销售量20 用户评价:comment rank 5()
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商品描述

商品属性

Target:Transferrin

Fields:HIF-1 signaling pathway;Ferroptosis;Mineral absorption

Gene Name:TF

Protein Name:Serotransferrin (Transferrin) (Beta-1 metal-binding globulin) (Siderophilin)

Human Gene Id:7018

Human Swiss Prot No:P02787

Mouse Swiss Prot No:Q921I1

Immunogen:Protein

Specificity:Transferrin protein detects endogenous levels of Transferrin

Formulation:Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

Source:Monoclonal, Mouse

Dilution:WB 1:2000-5000, IHC 1:100-200. IF 1:50-200

Purification:The antibody was affinity-purified from mouse ascites by affinity-chromatography using specific immunogen.

Concentration:1 mg/ml

Storage Stability:-15°C to -25°C/1 year(Do not lower than -25°C)

Other Name:TF;Serotransferrin;Transferrin;Beta-1 metal-binding globulin;Siderophilin

Observed Band(KD):77kD

Background:transferrin(TF) Homo sapiens This gene encodes a glycoprotein with an approximate molecular weight of 76.5 kDa. It is thought to have been created as a result of an ancient gene duplication event that led to generation of homologous C and N-terminal domains each of which binds one ion of ferric iron. The function of this protein is to transport iron from the intestine, reticuloendothelial system, and liver parenchymal cells to all proliferating cells in the body. This protein may also have a physiologic role as granulocyte/pollen-binding protein (GPBP) involved in the removal of certain organic matter and allergens from serum. [provided by RefSeq, Sep 2009],

Function:disease:Defects in TF are the cause of atransferrinemia [MIM:209300]. Atransferrinemia is rare autosomal recessive disorder characterized by iron overload and hypochromic anemia.,function:Transferrins are iron binding transport proteins which can bind two Fe(3+) ions in association with the binding of an anion, usually bicarbonate. It is responsible for the transport of iron from sites of absorption and heme degradation to those of storage and utilization. Serum transferrin may also have a further role in stimulating cell proliferation.,online information:Transferrin entry,polymorphism:Different polymorphic variants of transferrin are known. The sequence shown is the predominant electrophoretic variant (C1 or TF*C1).,similarity:Belongs to the transferrin family.,similarity:Contains 2 transferrin-like domains.,subunit:Monomer.,tissue specificity:Expressed by the liver and secreted in plas

Subcellular Location:Secreted.

Expression:Expressed by the liver and secreted in plasma.

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