Anti-F13A1 Antibody (Clone#OTI3F6)

Anti-F13A1 Antibody (Clone#OTI3F6)

价格: ¥1060 - 2580

品牌:BOSTER 品牌认证

货号:MA02047

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克隆性 :Monoclonal

适应物种 :human, mouse, rat

保质期 :发货周期:5-7天

库存 :9999

供应商 :博士德生物

应用范围 :WB, IHC

规格 :50μl/100μl/150μl

产品概况

货号 MA02047
产品名称 Anti-F13A1 Antibody (Clone#OTI3F6)
基因名 F13A1
抗体来源 Mouse
克隆 OTI3F6
抗体亚型 Mouse IgG1
分子量 79.2KD
免疫原 Full length human recombinant protein of human F13A1 (NP_000120) produced in HEK293T cell.
内容 PBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
纯化方式 Purified from mouse ascites fluids or tissue culture supernatant by affinity chromatography (protein A/G)
浓度 500 ug/ml
产品形态 Liquid
保存条件 Stable for 12 months from date of receipt. Store at -20°C as received.
背景资料 This gene encodes the coagulation factor XIII A subunit. Coagulation factor XIII is the last zymogen to become activated in the blood coagulation cascade. Plasma factor XIII is a heterotetramer composed of 2 A subunits and 2 B subunits. The A subunits have catalytic function, and the B subunits do not have enzymatic activity and may serve as plasma carrier molecules. Platelet factor XIII is comprised only of 2 A subunits, which are identical to those of plasma origin. Upon cleavage of the activation peptide by thrombin and in the presence of calcium ion, the plasma factor XIII dissociates its B subunits and yields the same active enzyme, factor XIIIa, as platelet factor XIII. This enzyme acts as a transglutaminase to catalyze the formation of gamma-glutamyl-epsilon-lysine crosslinking between fibrin molecules, thus stabilizing the fibrin clot. It also crosslinks alpha-2-plasmin inhibitor, or fibronectin, to the alpha chains of fibrin. Factor XIII deficiency is classified into two categories: type I deficiency, characterized by the lack of both the A and B subunits; and type II deficiency, characterized by the lack of the A subunit alone. These defects can result in a lifelong bleeding tendency, defective wound healing, and habitual abortion. [provided by RefSeq, Jul 2008]
研究类别 1. AbdAlla, S., Lother, H., Langer, A., el Faramawy, Y., Quitterer, U. Factor XIIIA transglutaminase crosslinks AT1 receptor dimers of monocytes at the onset of atherosclerosis. Cell 119: 343-354, 2004. 2. Anwar, R., Langlois, S. The arg703-to-trp missense mutation in F13A1 is a de novo event. Brit. J. Haemat. 146: 118-120, 2009. 3. Ariens, R. A. S., Philippou, H., Nagaswami, C., Weisel, J. W., Lane, D. A., Grant, P. J. The factor XIII V34L polymorphism accelerates thrombin activation of factor XIII and affects cross-linked fibrin structure. Blood 96: 988-995, 2000.
Uniprot ID F13A1: P00488

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[list_product_images]Figure 1. Immunohistochemical staining of paraffin-embedded Human prostate tissue within the normal limits using anti-F13A1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120°C for 3min, MA02047)|Figure 2. Immunohistochemical staining of paraffin-embedded Human colon tissue within the normal limits using anti-F13A1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120°C for 3min, MA02047)|Figure 3. Immunohistochemical staining of paraffin-embedded Human pancreas tissue within the normal limits using anti-F13A1 mouse monoclonal antibody. (Heat-induced epitope retrieval by 10mM citric buffer, pH6.0, 120°C for 3min, MA02047)|Figure 4. HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY F13A1 (Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-F13A1. [/list_product_images]

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