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FA11 (heavy chain, Cleaved-Glu19) rabbit pAb

商品貨號： PLA004406

適應(yīng) 性： 人,小鼠

￥600元

規(guī)格：

40μL 100μL 200μL

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MSDS

說明書

商品描述

基因名稱： F11
蛋白名稱： FA11 (heavy chain, Cleaved-Glu19)
Human_gene_id： 2160
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2160
Human_swiss_prot_no： P03951
Human_swiss_link： https://www.uniprot.org/uniprotkb/P03951/entry
Mouse_gene_id： 109821
Mouse_gene_link： https://www.uniprot.org/uniprot/109821
Mouse_swiss_prot_no： Q91Y47
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q91Y47
特異性： This antibody detects endogenous levels of Human, Mouse FA11 (heavy chain, Cleaved-Glu19, protein was cleaved amino acid sequence between 18-19 )
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:1000-2000 ELISA 1:5000-20000
純化工藝： The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： Coagulation factor XI (FXI;EC 3.4.21.27;Plasma thromboplastin antecedent;PTA) [Cleaved into: Coagulation factor XIa heavy chain; Coagulation factor XIa light chain]
實(shí)測條帶： 40 66kD
功能： catalytic activity:Selective cleavage of Arg-|-Ala and Arg-|-Val bonds in factor IX to form factor IXa.,disease:Defects in F11 are the cause of F11 deficiency [MIM:612416]; also called plasma thromboplastin antecedent deficiency or Rosenthal syndrome. It is a blood coagulation abnormality occurring in high frequency in Ashkenazi jews. F11-deficient patients are prone to excessive bleeding after haemostatic challenge.,function:Factor XI triggers the middle phase of the intrinsic pathway of blood coagulation by activating factor IX.,online information:Factor XI entry,PTM:Activated by factor XIIa (or XII), which cleaves each polypeptide after Arg-387 into the light chain, which contains the active site, and the heavy chain, which associates with high molecular weight (HMW) kininogen.,similarity:Belongs to the peptidase S1 family. Plasma kallikrein subfamily.,similarity:Contains 1 peptidase S1 domain.,similarity:Contains 4 apple domains.,subunit:Homodimer; disulfide-linked. After activation the heavy and light chains are also linked by a disulfide bond.,tissue specificity:Isoform 2 is produced by platelets and megakaryocytes but absent from other blood cells.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3053
細(xì)胞定位： Secreted.
組織表達(dá)： Isoform 2 is produced by platelets and megakaryocytes but absent from other blood cells.
科研貨號： PLA004406

FA11 (heavy chain, Cleaved-Glu19) rabbit pAb

Catalog No PLA004406

Product information

基因名稱： F11
蛋白名稱： FA11 (heavy chain, Cleaved-Glu19)
Human_gene_id： 2160
Human_gene_link： http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=2160
Human_swiss_prot_no： P03951
Human_swiss_link： https://www.uniprot.org/uniprotkb/P03951/entry
Mouse_gene_id： 109821
Mouse_gene_link： https://www.uniprot.org/uniprot/109821
Mouse_swiss_prot_no： Q91Y47
Mouse_swiss_link： https://www.uniprot.org/uniprotkb/Q91Y47
特異性： This antibody detects endogenous levels of Human, Mouse FA11 (heavy chain, Cleaved-Glu19, protein was cleaved amino acid sequence between 18-19 )
組成： Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
來源： Polyclonal, Rabbit,IgG
稀釋： WB 1:1000-2000 ELISA 1:5000-20000
純化工藝： The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
濃度： 1 mg/ml
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
說明書： 1
Msds： MSDS_Antibody.pdf
其他名稱： Coagulation factor XI (FXI;EC 3.4.21.27;Plasma thromboplastin antecedent;PTA) [Cleaved into: Coagulation factor XIa heavy chain; Coagulation factor XIa light chain]
實(shí)測條帶： 40 66kD
功能： catalytic activity:Selective cleavage of Arg-|-Ala and Arg-|-Val bonds in factor IX to form factor IXa.,disease:Defects in F11 are the cause of F11 deficiency [MIM:612416]; also called plasma thromboplastin antecedent deficiency or Rosenthal syndrome. It is a blood coagulation abnormality occurring in high frequency in Ashkenazi jews. F11-deficient patients are prone to excessive bleeding after haemostatic challenge.,function:Factor XI triggers the middle phase of the intrinsic pathway of blood coagulation by activating factor IX.,online information:Factor XI entry,PTM:Activated by factor XIIa (or XII), which cleaves each polypeptide after Arg-387 into the light chain, which contains the active site, and the heavy chain, which associates with high molecular weight (HMW) kininogen.,similarity:Belongs to the peptidase S1 family. Plasma kallikrein subfamily.,similarity:Contains 1 peptidase S1 domain.,similarity:Contains 4 apple domains.,subunit:Homodimer; disulfide-linked. After activation the heavy and light chains are also linked by a disulfide bond.,tissue specificity:Isoform 2 is produced by platelets and megakaryocytes but absent from other blood cells.,
相關(guān)產(chǎn)品： RS0001,RS0002,YM3028,YM3053
細(xì)胞定位： Secreted.
組織表達(dá)： Isoform 2 is produced by platelets and megakaryocytes but absent from other blood cells.
科研貨號： PLA004406

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