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STAT5B (Phospho Tyr694) Rabbit pAb

-YP1515

5 2
主要信息
Target

STAT5B Phospho Tyr694

Host Species

Rabbit

Reactivity

Human, Mouse

Applications

WB, IHC

MW

90kD (Observed)

Conjugate/Modification

Phospho

货号: YP1515
规格
价格
货期
数量
200μL
¥4,680.00
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0

100μL
¥2,800.00
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50μL
¥1,500.00
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详细信息
推荐稀释比
WB 1:500-2000; IHC 1:50-300
组成
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
特异性
This antibody detects endogenous levels of Human Mouse Stat5 (phospho-Tyr694)
纯化工艺
The antibody was affinity-purified from rabbit serum by affinity-chromatography using 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
90kD
修饰
Phospho
克隆性
Polyclonal
同种型
IgG
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抗原&靶点信息
免疫原:
Synthesized phosho peptide around human Stat5 (Tyr694)
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特异性:
This antibody detects endogenous levels of Human Mouse Stat5 (phospho-Tyr694)
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基因名称:
STAT5B
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蛋白名称:
Signal transducer and activator of transcription 5B (Tyr694)
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别名:
Signal transducer and activator of transcription 5B
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数据库链接:
Organism 基因 ID SwissProt
Human 6777; P51692;
Mouse 20851; P42232;
Rat 25126; P52632;
背景:
The protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors , STAT family members are phosphorylated by the receptor associated kinases , and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein mediates the signal transduction triggered by various cell ligands , such as IL2 , IL4 , CSF1 , and different growth hormones. It has been shown to be involved in diverse biological processes , such as TCR signaling , apoptosis , adult mammary gland development , and sexual dimorphism of liver gene expression. This gene was found to fuse to retinoic acid receptor-alpha (RARA) gene in a small subset of acute promyelocytic leukemias (APLL) . The dysregulation of the signaling pathways mediated by this protein may be the cause of the APLL. [provi
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功能:
Disease:Defects in STAT5B are the cause of Laron type dwarfism II (LTD2) [MIM:245590]; also known as Laron syndrome type II or Laron syndrome due to a post-receptor defect. The phenotypic features are consistent with growth hormone deficiency in the presence of normal to elevated circulating concentrations of growth hormone , and resistance to hexogeneous hormone therapy. ,Function:Carries out a dual Function: signal transduction and activation of transcription. Binds to the GAS element and activates PRL-induced transcription. ,online information:STAT5 entry ,online information:STAT5B mutation db ,PTM:Tyrosine phosphorylated. ,similarity:Belongs to the transcription factor STAT family. ,similarity:Contains 1 SH2 domain. ,subcellular location:Translocated into the nucleus in response to phosphorylation. ,subunit:Forms a homodimer or a heterodimer with a related family member. Binds NR3C1 (By similarity) . Interacts with NCOA1 , NMI and SOCS7. ,
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细胞定位:
Cytoplasm . Nucleus . Translocated into the nucleus in response to phosphorylation. .
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组织表达:
研究领域:
>>ErbB signaling pathway ;
>>Chemokine signaling pathway ;
>>Necroptosis ;
>>JAK-STAT signaling pathway ;
>>Th1 and Th2 cell differentiation ;
>>Th17 cell differentiation ;
>>Prolactin signaling pathway ;
>>AGE-RAGE signaling pathway in diabetic complications ;
>>Growth hormone synthesis , secretion and action ;
>>Hepatitis B ;
>>Measles ;
>>Human T-cell leukemia virus 1 infection ;
>>Pathways in cancer ;
>>Viral carcinogenesis ;
>>Chemical carcinogenesis - receptor activation ;
>>Chronic myeloid leukemia ;
>>Acute myeloid leukemia ;
>>Non-small cell lung cancer
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货号: YP1515
规格
价格
货期
数量
200μL
¥4,680.00
现货

0

100μL
¥2,800.00
现货

0

50μL
¥1,500.00
现货

0

加入购物车

已收藏

收藏

定制服务咨询
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