Product Name	Factor VII heavy chain
Chinese Name	凝血因子7抗体
Alias	Factor VII heavy chain; coagulation factor VII (serum prothrombin conversion accelerator); Coagulation factor VII; Eptacog alfa; F7; FA7_HUMAN; Factor VII; Factor VII light chain; FVII coagulation protein; OTTHUMP00000018733; OTTHUMP00000018734; Proconvertin; Serum prothrombin conversion accelerator; SPCA.
literatures	Specific References  (2)     |     SL4846R has been referenced in 2 publications. [IF=4.307] Devin Cao. et al. Vascular Endothelial Cells Produce Coagulation Factors That Control Their Growth via Joint Protease-Activated Receptor and C5a Receptor 1 (CD88) Signaling. Am J Pathol. 2022 Feb;192:361  IF ;  Mouse.   PubMed:35144762 [IF=2.93] Liu, Yang, et al. "A Simple Method for Isolating and Culturing the Rat Brain Microvascular Endothelial Cells." Microvascular Research (2013).  Rat.   PubMed:23978334
Research Area	Cardiovascular  Cell biology  immunology
Immunogen Species	Rabbit
Clonality	Polyclonal
React Species	Human,
Applications	WB=1:500-2000 ELISA=1:5000-10000 IHC-P=1:100-500 IHC-F=1:100-500 IF=1:50-200 （Paraffin sections need antigen repair） not yet tested in other applications. optimal dilutions/concentrations should be determined by the end user.
Theoretical molecular weight	17/28kDa
Cellular localization	Secretory protein
Form	Liquid
Concentration	1mg/ml
immunogen	KLH conjugated synthetic peptide derived from human Factor VII heavy chain: 301-400/466
Lsotype	IgG
Purification	affinity purified by Protein A
Buffer Solution	0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
Storage	Shipped at 4℃. Store at -20 °C for one year. Avoid repeated freeze/thaw cycles.
Attention	This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed	PubMed
Product Detail	Initiates the extrinsic pathway of blood coagulation. Serine protease that circulates in the blood in a zymogen form. Factor VII is converted to factor VIIa by factor Xa, factor XIIa, factor IXa, or thrombin by minor proteolysis. In the presence of tissue factor and calcium ions, factor VIIa then converts factor X to factor Xa by limited proteolysis. Factor VIIa will also convert factor IX to factor IXa in the presence of tissue factor and calcium. Function: Initiates the extrinsic pathway of blood coagulation. Serine protease that circulates in the blood in a zymogen form. Factor VII is converted to factor VIIa by factor Xa, factor XIIa, factor IXa, or thrombin by minor proteolysis. In the presence of tissue factor and calcium ions, factor VIIa then converts factor X to factor Xa by limited proteolysis. Factor VIIa will also convert factor IX to factor IXa in the presence of tissue factor and calcium. Subunit: Heterodimer of a light chain and a heavy chain linked by a disulfide bond. Subcellular Location: Secreted. Tissue Specificity: Plasma. Post-translational modifications: The vitamin K-dependent, enzymatic carboxylation of some glutamate residues allows the modified protein to bind calcium. The iron and 2-oxoglutarate dependent 3-hydroxylation of aspartate and asparagine is (R) stereospecific within EGF domains. DISEASE: Defects in F7 are the cause of factor VII deficiency (FA7D) [MIM:227500]. A hemorrhagic disease with variable presentation. The clinical picture can be very severe, with the early occurrence of intracerebral hemorrhages or repeated hemarthroses, or, in contrast, moderate with cutaneous-mucosal hemorrhages (epistaxis, menorrhagia) or hemorrhages provoked by a surgical intervention. Finally, numerous subjects are completely asymptomatic despite very low factor VII levels. Similarity: Belongs to the peptidase S1 family. Contains 2 EGF-like domains. Contains 1 Gla (gamma-carboxy-glutamate) domain. Contains 1 peptidase S1 domain. SWISS: P08709 Gene ID: 2155 Database links: Entrez Gene: 2155 Human Omim: 613878 Human SwissProt: P08709 Human Unigene: 36989 Human 凝血因子7是肝脏合成的一种维生素K依赖性的单链glycoprotein,由4 0 6个氨基酸残基组成,分子量约45kD。 凝血因子Ⅶ的半衰期最短（4～6h），血浆含量较低（0.5～2mg/L），故可作为肝病患者蛋白质合成功能减退的早期诊断指标。在慢性肝病患者通过肝活检组织原位杂交的方法检测到凝血因子Ⅶ的表达与肝纤维化的分级呈负相关，可作为预测纤维化程度的指标。凝血因子Ⅶ活性还与预后有着密切的联系，经研究认为：凝血因子Ⅶ活性<34%的肝硬化患者93%在随访10月内死亡，故认为它是肝硬化患者预后好坏的早期预测指标，可更好识别肝移植候选人。肝硬化患者凝血因子Ⅶ活性可明显下降，凝血因子Ⅶ缺乏可导致血小板活性的改变，结合血小板计数减少使出血时间延长，因此对有创诊断与治疗的肝硬化患者，还应该用凝血因子Ⅶ活性进行出血危险度的评估，而不能仅看血小板计数。除诊断之外，重组凝血因子Ⅶ可以有效地纠正肝病患者凝血异常，有利于有创性检查的进行。
Product Picture	Sample: Jurkat(Human) Cell Lysate at 30 ug Primary: Anti- Factor VII heavy chain (SL4846R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 17/28 kD Observed band size: 50 kD Sample: Lane 1: Human HepG2 cell lysates Primary: Anti-Factor VII heavy chain (SL4846R) at 1/1000 dilution Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution Predicted band size: 17/28 kDa Observed band size: 59 kDa

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