Fibrinogen γ Monoclonal Antibody

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商品货号： PLA004805

适应性： 人

￥600元

规格：

40μL 100μL 200μL

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MSDS

说明书

商品描述

发货日期： 7
基因名称： FGG
蛋白名称： Fibrinogen gamma chain
Human_gene_id： 2266
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2266
Human_swiss_prot_no： P02679
Human_swiss_link： http://www.uniprot.org/uniprotkb/P02679/entry
Mouse_swiss_prot_no： Q8VCM7
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q8VCM7
特异性： Fibrinogen γ Monoclonal Antibody detects endogenous levels of Fibrinogen γ protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Monoclonal, Mouse
稀释： WB 1:500 - 1:2000. IHC 1:200 - 1:1000. IF 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
纯化工艺： Affinity purification
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： FGG; Fibrinogen gamma chain
信号通路： Complement and coagulation cascades;
功能： disease:Defects in FGG are a cause of congenital afibrinogenemia [MIM:202400]. It is a rare autosomal recessive disorder characterized by complete absence of detectable fibrinogen.,disease:Defects in FGG are a cause of thrombophilia.,domain:A long coiled coil structure formed by 3 polypeptide chains connects the central nodule to the C-terminal domains (distal nodules). The long C-terminal ends of the alpha chains fold back, contributing a fourth strand to the coiled coil structure.,function:Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation.,miscellaneous:The gamma-chain carries the main binding site for the platelet receptor.,online information:Fibrinogen entry,PTM:Conversion of fibrinogen to fibrin is triggered by thrombin, which cleaves fibrinopeptides A and B from alpha and beta chains, and thus exposes the N-terminal polymerization sites responsible for the formation of the soft clot. The soft clot is converted into the hard clot by factor XIIIA which catalyzes the epsilon-(gamma-glutamyl)lysine cross-linking between gamma chains (stronger) and between alpha chains (weaker) of different monomers.,PTM:Sulfation of C-terminal tyrosines increases affinity for thrombin.,similarity:Contains 1 fibrinogen C-terminal domain.,subunit:Heterohexamer; disulfide linked. Contains 2 sets of 3 non-identical chains (alpha, beta and gamma). The 2 heterotrimers are in head to head conformation with the N-termini in a small central domain.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Secreted .
组织表达： Detected in blood plasma (at protein level).
科研货号： PLA004805

Fibrinogen γ Monoclonal Antibody

Catalog No PLA004805

Product information

发货日期： 7
基因名称： FGG
蛋白名称： Fibrinogen gamma chain
Human_gene_id： 2266
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2266
Human_swiss_prot_no： P02679
Human_swiss_link： http://www.uniprot.org/uniprotkb/P02679/entry
Mouse_swiss_prot_no： Q8VCM7
Mouse_swiss_link： http://www.uniprot.org/uniprot/Q8VCM7
特异性： Fibrinogen γ Monoclonal Antibody detects endogenous levels of Fibrinogen γ protein.
组成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
来源： Monoclonal, Mouse
稀释： WB 1:500 - 1:2000. IHC 1:200 - 1:1000. IF 1:200 - 1:1000. Flow cytometry: 1:200 - 1:400. ELISA: 1:10000. Not yet tested in other applications.
纯化工艺： Affinity purification
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
说明书： 1
Msds： MSDS_Antibody.pdf
其他名称： FGG; Fibrinogen gamma chain
信号通路： Complement and coagulation cascades;
功能： disease:Defects in FGG are a cause of congenital afibrinogenemia [MIM:202400]. It is a rare autosomal recessive disorder characterized by complete absence of detectable fibrinogen.,disease:Defects in FGG are a cause of thrombophilia.,domain:A long coiled coil structure formed by 3 polypeptide chains connects the central nodule to the C-terminal domains (distal nodules). The long C-terminal ends of the alpha chains fold back, contributing a fourth strand to the coiled coil structure.,function:Fibrinogen has a double function: yielding monomers that polymerize into fibrin and acting as a cofactor in platelet aggregation.,miscellaneous:The gamma-chain carries the main binding site for the platelet receptor.,online information:Fibrinogen entry,PTM:Conversion of fibrinogen to fibrin is triggered by thrombin, which cleaves fibrinopeptides A and B from alpha and beta chains, and thus exposes the N-terminal polymerization sites responsible for the formation of the soft clot. The soft clot is converted into the hard clot by factor XIIIA which catalyzes the epsilon-(gamma-glutamyl)lysine cross-linking between gamma chains (stronger) and between alpha chains (weaker) of different monomers.,PTM:Sulfation of C-terminal tyrosines increases affinity for thrombin.,similarity:Contains 1 fibrinogen C-terminal domain.,subunit:Heterohexamer; disulfide linked. Contains 2 sets of 3 non-identical chains (alpha, beta and gamma). The 2 heterotrimers are in head to head conformation with the N-termini in a small central domain.,
相关产品： RS0001,RS0002,YM3028,YM3029
细胞定位： Secreted .
组织表达： Detected in blood plasma (at protein level).
科研货号： PLA004805

Hunan UPT Biotechnology Co.,Ltd

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E-mail：service@uptbio.com

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