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ZBTB12 Rabbit pAb (bs-13565R)  
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50ul/1180.00元
100ul/1980.00元
200ul/2800.00元
大包装/询价
产品编号 bs-13565R
英文名称 ZBTB12 Rabbit pAb
中文名称 锌指蛋白ZBTB12抗体
别    名 Bat9; C6orf46; G10; HLA B associated transcript 9; NG35; Protein G10; ZBT12_HUMAN; ZBTB12; Zinc finger and BTB domain containing protein 12; Zinc finger and BTB domain-containing protein 12.  
研究领域 细胞生物  信号转导  锌指蛋白  表观遗传学  
抗体来源 Rabbit
克隆类型 Polyclonal
交叉反应 (predicted: Human,Mouse,Rat,Pig,Sheep,Cow,Dog)
产品应用 WB=1:500-2000,ELISA=1:5000-10000
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 49 kDa
检测分子量
细胞定位 细胞核 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human ZBTB12: 21-120/459 
亚    型 IgG
纯化方法 affinity purified by Protein A
缓 冲 液 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
保存条件 Shipped at 4℃. Store at -20℃ for one year. Avoid repeated freeze/thaw cycles.
注意事项 This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
PubMed PubMed
产品介绍 ZBTB12 is a 459 amino acid protein that may be involved in transcriptional regulation. BAT9 localizes to nucleus, contains one BTB (POZ) domain and four C2H2-type zinc fingers. The BAT9 gene maps to human chromosome 6p21.32. Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6.

Function:
May be involved in transcriptional regulation.

Subcellular Location:
Nucleus.

Similarity:
Contains 1 BTB (POZ) domain.
Contains 4 C2H2-type zinc fingers.

SWISS:
Q9Y330

Gene ID:
221527

Database links:

Entrez Gene: 221527 Human

SwissProt: Q9Y330 Human

Unigene: 234027 Human



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