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BMPR-II rabbit pAb

说明书

BYab-13769

  • 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)
免疫原
Synthesized peptide derived from human BMPR-II
特异性
This antibody detects endogenous levels of Human,Mouse,Rat,Monkey BMPR-II
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
WB 1:1000-2000 ELISA 1:5000-20000
纯化工艺(Immunogen)
The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
浓度
1 mg/ml
背景(Background)
This gene encodes a member of the bone morphogenetic protein (BMP) receptor family of transmembrane serine/threonine kinases. The ligands of this receptor are BMPs, which are members of the TGF-beta superfamily. BMPs are involved in endochondral bone formation and embryogenesis. These proteins transduce their signals through the formation of heteromeric complexes of two different types of serine (threonine) kinase receptors: type I receptors of about 50-55 kD and type II receptors of about 70-80 kD. Type II receptors bind ligands in the absence of type I receptors, but they require their respective type I receptors for signaling, whereas type I receptors require their respective type II receptors for ligand binding. Mutations in this gene have been associated with primary pulmonary hypertension, both familial and fenfluramine-associated, and with pulmonary venoocclusive disea
功能
catalytic activity:ATP + [receptor-protein] = ADP + [receptor-protein] phosphate.,cofactor:Magnesium or manganese.,disease:Defects in BMPR2 are a cause of pulmonary venoocclusive disease (PVOD) [MIM:265450]. PVOD is a rare form of pulmonary hypertension in which the vascular changes originate in the small pulmonary veins and venules. The pathogenesis is unknown and any link with PPH1 has been speculative. The finding of PVOD associated with a BMPR2 mutation reveals a possible pathogenetic connection with PPH1.,disease:Defects in BMPR2 are the cause of primary pulmonary hypertension (PPH1) [MIM:178600]. PPH1 is a rare autosomal dominant disorder characterized by plexiform lesions of proliferating endothelial cells in pulmonary arterioles. The lesions lead to elevated pulmonary arterial pression, right ventricular failure, and death. The disease can occur from infancy throughout life and i
基因名称(Gene Name)
BMPR2 PPH1
蛋白名称
BMPR-II
简称
BMPR-II
其他名称
Bone morphogenetic protein receptor type-2 (BMP type-2 receptor;BMPR-2;EC 2.7.11.30;Bone morphogenetic protein receptor type II;BMP type II receptor;BMPR-II)
Fields
>>Cytokine-cytokine receptor interaction;>>TGF-beta signaling pathway;>>Axon guidance;>>Hippo signaling pathway;>>Signaling pathways regulating pluripotency of stem cells;>>MicroRNAs in cancer;>>Fluid shear stress and atherosclerosis
人基因ID
659
人蛋白质序列数据库
Q13873
小鼠基因ID
12168
小鼠蛋白质序列数据库
O35607
大鼠基因ID
大鼠蛋白质序列数据库
细胞定位
Cell membrane ; Single-pass type I membrane protein.
组织表达
Highly expressed in heart and liver.
储存(Storage)
-20°C/1 year

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BMPR-II rabbit pAb

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