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TXA synthase Polyclonal Antibody

说明书

BYab-13970

  • 20UL ¥460 50UL ¥945 100UL ¥1350
  • 货期: 3天左右

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宿主
反应性
应用
WB;ELISA
分子量(DA)
60kD
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.
来源
Polyclonal, Rabbit,IgG
组成(Formulation)
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
稀释比例
Western Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.
纯化工艺(Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
浓度
1 mg/ml
背景(Background)
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],
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 lu
基因名称(Gene Name)
TBXAS1
蛋白名称
Thromboxane-A synthase
简称
TXA synthase
其他名称
TBXAS1; CYP5; CYP5A1; Thromboxane-A synthase; TXA synthase; TXS; Cytochrome P450 5A1
Fields
>>Arachidonic acid metabolism;>>Metabolic pathways;>>Platelet activation
人基因ID
6916
人蛋白质序列数据库
P24557
小鼠基因ID
小鼠蛋白质序列数据库
P36423
大鼠基因ID
大鼠蛋白质序列数据库
细胞定位
Endoplasmic reticulum membrane ; Multi-pass membrane protein .
组织表达
Platelets, lung, kidney, spleen, macrophages and lung fibroblasts.
储存(Storage)
-20°C/1 year

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TXA synthase Polyclonal Antibody

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