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NKAIN2 Rabbit pAb (bs-19259R)  
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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-19259R
英文名称 NKAIN2 Rabbit pAb
中文名称 钠/钾转运ATP酶相互作用蛋白2抗体
别    名 FAM77B; Na(+)/K(+)-transporting ATPase subunit beta-1-interacting protein 2; Na+/K+TRANSPORTING ATPase-INTERACTING PROTEIN 2; NKAI2_HUMAN; NKAIN2; NKAIP2; Protein FAM77B; SODIUM/POTASSIUM TRANSPORTING ATPase-INTERACTING PROTEIN 2; Sodium/potassium-transporting ATPase subunit beta-1-interacting protein 2; T-CELL LYMPHOMA BREAKPOINT-ASSOCIATED TARGET 1; ; T-cell lymphoma breakpoint-associated target protein 1; TCBA1.  
研究领域 细胞生物  信号转导  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 (predicted: Human,Mouse,Cow)
产品应用 IHC-P=1:100-500,IHC-F=1:100-500,IF=1:100-500,ICC/IF=1:100-500
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
理论分子量 24 kDa
检测分子量
细胞定位 细胞膜 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human NKAIN2: 31-130/208 
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 This gene encodes a transmembrane protein that interacts with the beta subunit of a sodium/potassium-transporting ATPase. A chromosomal translocation involving this gene is a cause of lymphoma. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2014]

Subcellular Location:
Cell membrane.

Tissue Specificity:
Expressed in fetal brain. Weakly expressed in adult brain and thymus. Not expressed in any other normal tissue examined.

DISEASE:
Note=A chromosomal aberration involving NKAIN2 is a cause of lymphoma. Deletion del(6)(q13q21) within NKAIN2 and involving SUSP1 generates the SUSP1-NKAIN2 product.

Similarity:
Belongs to the NKAIN family.

SWISS:
Q5VXU1

Gene ID:
154215

Database links:

Entrez Gene: 154215 Human

Omim: 609758 Human

SwissProt: Q5VXU1 Human

Unigene: 656604 Human



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