产品名称
TXA synthase Rabbit Polyclonal Antibody
别名
TBXAS1; CYP5; CYP5A1; Thromboxane-A synthase; TXA synthase; TXS; Cytochrome P450 5A1
蛋白名称
Thromboxane-A synthase
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene Link
http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&term=6916
Human Swissprot No.
P24557
Human Swissprot Link
http://www.uniprot.org/uniprotkb/P24557/entry
Mouse Swissprot No.
P36423
Mouse Swissprot Link
http://www.uniprot.org/uniprot/P36423
免疫原
Synthesized peptide derived from the C-terminal region of human TXA synthase.
特异性
TXA synthase Polyclonal Antibody detects endogenous levels of TXA synthase protein.
稀释度
WB 1:500 - 1:2000. ELISA: 1:20000. Not yet tested in other applications.
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. However, this protein is considered a member of the cytochrome P450 superfamily on the basis of sequence similarity rather than functional similarity. This endoplasmic reticulum membrane protein catalyzes the conversion of prostglandin H2 to thromboxane A2, a potent vasoconstrictor and inducer of platelet aggregation. The enzyme plays a role in several pathophysiological processes including hemostasis, cardiovascular disease, and stroke. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2008],
组织表达
Platelets, lung, kidney, spleen, macrophages and lung fibroblasts.
细胞定位
Endoplasmic reticulum membrane ; Multi-pass membrane protein .
信号通路
Arachidonic acid metabolism;
功能
catalytic activity:(5Z,13E)-(15S)-9-alpha,11-alpha-epidioxy-15-hydroxyprosta-5,13-dienoate = (5Z,13E)-(15S)-9-alpha,11-alpha-epoxy-15-hydroxythromboxa-5,13-dienoate.,cofactor:Heme group.,disease:Defects in TBXAS1 are the cause of Ghosal hematodiaphyseal dysplasia (GHDD) [MIM:231095]. GHDD is a rare autosomal recessive disorder characterized by increased bone density with predominant diaphyseal involvement and aregenerative corticosteroid-sensitive anemia. Aregenerative anemia is characterized by bone marrow failure, so that functional marrow cells are regenerated slowly or not at all.,disease:Defects in TBXAS1 are the cause of thromboxane synthetase deficiency [MIM:274180]. It is characterized by hemorrhagic diathesis.,online information:CYP5A1 alleles,similarity:Belongs to the cytochrome P450 family.,subunit:Monomer.,tissue specificity:Platelets, lung, kidney, spleen, macrophages and lung fibroblasts.,
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
