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ANTR2 Rabbit pAb

-YN2043

2 5
主要信息
Target

ANTR2

Host Species

Rabbit

Reactivity

Human, Mouse

Applications

WB, ELISA

MW

53kD (Observed)

Conjugate/Modification

Unmodified

货号: YN2043
规格
价格
货期
数量
200μL
¥3,780.00
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0

100μL
¥2,300.00
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0

40μL
¥960.00
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0

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详细信息
推荐稀释比
WB 1:500-2000; ELISA 1:5000-20000
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
特异性
ANTR2 Polyclonal Antibody detects endogenous levels of protein.
纯化工艺
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
浓度
1 mg/ml
实测条带
53kD
修饰
Unmodified
克隆性
Polyclonal
同种型
IgG
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抗原&靶点信息
免疫原:
Synthesized peptide derived from part region of human protein
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特异性:
ANTR2 Polyclonal Antibody detects endogenous levels of protein.
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基因名称:
ANTXR2 CMG2
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蛋白名称:
Anthrax toxin receptor 2 (Capillary morphogenesis gene 2 protein) (CMG-2)
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数据库链接:
Organism 基因 ID SwissProt
Human 118429; P58335;
Mouse Q6DFX2;
背景:
This gene encodes a receptor for anthrax toxin. The protein binds to collagen IV and laminin, suggesting that it may be involved in extracellular matrix adhesion. Mutations in this gene cause juvenile hyaline fibromatosis and infantile systemic hyalinosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Mar 2009],
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功能:
Disease:Defects in ANTXR2 are the cause of infantile systemic hyalinosis (ISH) [MIM:236490]. This autosomal recessive syndrome is similar to JHF, but has an earlier onset and a more severe course. Symptoms appear at birth or within the first months of life, with painful, swollen joint contractures, osteopenia, osteoporosis and livid red hyperpigmentation over bony prominences. Patients develop multiple subcutaneous skin tumors and gingival hypertrophy. Hyaline deposits in multiple organs, recurrent infections and intractable diarrhea often lead to death within the first 2 years of life. Surviving children may suffer from severely reduced mobility due to joint contractures.,Disease:Defects in ANTXR2 are the cause of juvenile hyaline fibromatosis (JHF) [MIM:228600]. JHF is an autosomal recessive syndrome that is similar to ISH but takes a milder course. It is characterized by hyaline deposition in the dermis, multiple subcutaneous skin tumors and gingival hypertrophy, followed by progressive joint contractions, osteopenia and osteoporosis that may lead to a severe limitation of mobility.,Domain:Binding to PA seems to be effected through the VWA domain.,Function:Necessary for cellular interactions with laminin and the extracellular matrix.,miscellaneous:Upon binding of the protective antigen (PA) of Bacillus anthracis the complex moves to glycosphingolipid-rich lipid rafts, where it is internalized via a clathrin-dependent pathway.,similarity:Belongs to the ATR family.,similarity:Contains 1 VWFA domain.,subcellular location:Expressed at the cell surface.,subcellular location:Expressed predominantly within the endoplasmic reticulum and not at the plasma membrane.,subunit:Binds laminin, and possibly also collagen type IV. Binds to the protective antigen (PA) of Bacillus anthracis in a divalent cation-dependent manner, with the following preference: calcium > manganese > magnesium > zinc. Binding of PA leads to heptamerization of the receptor-PA complex.,tissue specificity:Expressed in prostate, thymus, ovary, testis, pancreas, colon, heart, kidney, lung, liver, peripheral blood leukocytes, placenta, skeletal muscle, small intestine and spleen.,
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细胞定位:
[Isoform 1]: Cell membrane ; Single-pass type I membrane protein . Expressed at the cell surface. .; [Isoform 2]: Endoplasmic reticulum membrane ; Single-pass type I membrane protein . Expressed predominantly within the endoplasmic reticulum and not at the plasma membrane. .; [Isoform 3]: Secreted .
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研究领域:
>>NOD-like receptor signaling pathway
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货号: YN2043
规格
价格
货期
数量
200μL
¥3,780.00
现货

0

100μL
¥2,300.00
现货

0

40μL
¥960.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询

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