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AP2B Rabbit Polyclonal Antibody

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产品基本信息

产品货号
BD-PN3852
产品名称
AP2B Rabbit Polyclonal Antibody
类别
常规抗体
基因名称
TFAP2B
蛋白名称
AP2B
推荐应用
WB
反应种属
Human,Mouse
浓度
1 mg/ml
存储缓冲液
Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% New type preservative N.
Human Gene ID
7021
Human Gene Link
https://www.uniprot.org/uniprot/7021
Human Swissprot No.
Q92481
Human Swissprot Link
https://www.uniprot.org/uniprotkb/Q92481/entry
Mouse Gene ID
21419
Mouse Gene Link
https://www.uniprot.org/uniprot/21419
Mouse Swissprot No.
Q61313
Mouse Swissprot Link
https://www.uniprot.org/uniprotkb/Q61313
免疫原
Synthesized peptide derived from human AP2B AA range: 18-68
特异性
This antibody detects endogenous levels of AP2B at Human/Mouse
稀释度
WB 1:500-2000
参考分子量
51kD
运输及保存条件
-20°C/1 year
宿主
Polyclonal, Rabbit,IgG
背景介绍
This gene encodes a member of the AP-2 family of transcription factors. AP-2 proteins form homo- or hetero-dimers with other AP-2 family members and bind specific DNA sequences. They are thought to stimulate cell proliferation and suppress terminal differentiation of specific cell types during embryonic development. Specific AP-2 family members differ in their expression patterns and binding affinity for different promoters. This protein functions as both a transcriptional activator and repressor. Mutations in this gene result in autosomal dominant Char syndrome, suggesting that this gene functions in the differentiation of neural crest cell derivatives. [provided by RefSeq, Jul 2008],
细胞定位
Nucleus . In the brain, localizes to the arcuate hypothalamic nucleus, the ventromedial hypothalamic nucleus and the accumbens nucleus of the ventral striatum. .
功能
disease:Defects in TFAP2B are the cause of Char syndrome (CHAR) [MIM:169100]. CHAR is an autosomal dominant disorder characterized by patent ductus arteriosus (PDA), facial dysmorphism and hand anomalies.,function:Sequence-specific DNA-binding protein that interacts with inducible viral and cellular enhancer elements to regulate transcription of selected genes. AP-2 factors bind to the consensus sequence 5'-GCCNNNGGC-3' and activate genes involved in a large spectrum of important biological functions including proper eye, face, body wall, limb and neural tube development. They also suppress a number of genes including MCAM/MUC18, C/EBP alpha and MYC. AP-2 beta appears to be required for normal face and limb development and for proper terminal differentiation and function of renal tubular epithelia.,online information:Activatin protein 2 entry,PTM:Sumoylated on Lys-21; which inhibits transcriptional activity.,similarity:Belongs to the AP-2 family.,subunit:Binds DNA as a dimer. Can form homodimers or heterodimers with other AP-2 family members. Interacts with CITED4. Interacts with UBE2I.,
期货
现货
纯化
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

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