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HDHD2B Rabbit pAb (bs-8319R)  
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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-8319R
英文名称 HDHD2B Rabbit pAb
中文名称 HDHD2B蛋白抗体
别    名 FLJ44846; FLJ46044; HDHD2B; hLHPP; lhpp; LHPP_HUMAN; phospholysine phosphohistidine inorganic pyrophosphate phosphatase.  
研究领域 肿瘤  细胞生物  免疫学  信号转导  转录调节因子  
抗体来源 Rabbit
克隆类型 Polyclonal
克 隆 号
交叉反应 (predicted: Human,Mouse,Rat,Rabbit,Pig,Cow,Dog,Horse)
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 29 kDa
检测分子量
细胞定位 细胞核 细胞浆 
性    状 Liquid
浓    度 1mg/ml
免 疫 原 KLH conjugated synthetic peptide derived from human HDHD2B/LHPP: 171-270/270 
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 LHPP, also known as HDHD2B, is a 270 amino acid protein that exists as a homodimer and is a member of the HAD-like hydrolase superfamily. Expressed in liver, kidney and moderately in brain, LHPP is encoded by a gene located on 10, which houses over 1,200 genes and comprises nearly 4.5% of the human genome. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.

Function:
Phosphatase that hydrolyzes imidodiphosphate, 3-phosphohistidine and 6-phospholysine. Has broad substrate specificity and can also hydrolyze inorganic diphosphate, but with lower efficiency (By similarity).

Subunit:
Homodimer.

Subcellular Location:
Cytoplasm. Nucleus.

Tissue Specificity:
Expressed in brain, and at lower levels in liver and kidney. Detected in thyroid (at protein level). Expressed in liver, kidney and moderately in brain.

Similarity:
Belongs to the HAD-like hydrolase superfamily.

SWISS:
Q9H008

Gene ID:
64077

Database links:

Entrez Gene: 64077 Human

Entrez Gene: 76429 Mouse

Entrez Gene: 361663 Rat

SwissProt: Q9H008 Human

SwissProt: Q9D7I5 Mouse

SwissProt: Q5I0D5 Rat

Unigene: 527748 Human

Unigene: 276721 Mouse

Unigene: 15275 Rat



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