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R

TCF-4 (PT1740R) PT™ Rabbit mAb

-YM9582

hot 5 2 10
主要信息
Target

TCF-4

Host Species

Rabbit

Reactivity

Human, Mouse

Applications

WB, IHC, IF, ELISA

MW

71kD (Calculated)

62kD (Observed)

Conjugate/Modification

Unmodified

货号: YM9582
规格
价格
货期
数量
200μL
¥3,580.00
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0

100μL
¥1,960.00
现货

0

40μL
¥960.00
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0

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详细信息
推荐稀释比
IHC 1:200-1:1000; WB 1:2000-1:10000; IF 1:200-1:1000; ELISA 1:5000-1:20000;
Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#YS0004)
组成
PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
特异性
Endogenous
纯化工艺
Protein A
储存
-15°C to -25°C/1 year(Do not lower than -25°C)
理论分子量
71kD
实测条带
62kD
修饰
Unmodified
克隆性
Monoclonal
克隆号
PT1740R
同种型
IgG,Kappa
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抗原&靶点信息
特异性:
Endogenous
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基因名称:
TCF4
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蛋白名称:
Transcription factor 4
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别名:
TCF4 ;
BHLHB19 ;
ITF2 ;
SEF2 ;
Transcription factor 4 ;
TCF-4 ;
Class B basic helix-loop-helix protein 19 ;
bHLHb19 ;
Immunoglobulin transcription factor 2 ;
ITF-2 ;
SL3-3 enhancer factor 2 ;
SEF-2 ;
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数据库链接:
Organism 基因 ID SwissProt
Human 6925; P15884;
Mouse 21413;
Rat 84382; Q62655;
背景:
This gene encodes transcription factor 4, a basic helix-loop-helix transcription factor. The encoded protein recognizes an Ephrussi-box ('E-box') binding site ('CANNTG') - a motif first identified in immunoglobulin enhancers. This gene is broadly expressed, and may play an important role in nervous system development. Defects in this gene are a cause of Pitt-Hopkins syndrome. In addition, an intronic CTG repeat normally numbering 10-37 repeat units can expand to >50 repeat units and cause Fuchs endothelial corneal dystrophy. Multiple alternatively spliced transcript variants that encode different proteins have been described. [provided by RefSeq, Jul 2016],
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功能:
Disease:Defects in TCF4 are a cause of Pitt-Hopkins syndrome (PTHS) [MIM:610954].,Disease:Haploinsufficiency of TCF4 is a cause of Pitt-Hopkins syndrome (PTHS) [MIM:610954]. PTHS is a rare syndromic encephalopathy characterized by severe psychomotor delay, epilepsy, daily bouts of diurnal hyperventilation starting in infancy, mild postnatal growth retardation, postnatal microcephaly, and distinctive facial features. Since most hitherto reported cases have been sporadic, with males and females equally affected, PTHS is regarded as an autosomal dominant condition.,Function:Transcription factor that binds to the immunoglobulin enchancer Mu-E5/KE5-motif. Binds to the E-box present in the somatostatin receptor 2 initiator element (SSTR2-INR) to activate transcription (By similarity). Preferentially binds to either 5'-ACANNTGT-3' or 5'-CCANNTGG-3'.,sequence Caution:Incomplete and probable erroneous sequence.,similarity:Contains 1 basic helix-loop-helix (bHLH) domain.,subunit:Efficient DNA binding requires dimerization with another bHLH protein. Forms homo- or heterooligomers with myogenin. Interacts with HIVEP2.,tissue specificity:Expressed in adult heart, brain, placenta, skeletal muscle and to a lesser extent in the lung. In developing embryonic tissues, expression mostly occurs in the brain.,
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细胞定位:
Nucleus .
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货号: YM9582
规格
价格
货期
数量
200μL
¥3,580.00
现货

0

100μL
¥1,960.00
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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