LHPP 抗体 (AA 171-270) (Cy3)
Quick Overview for LHPP 抗体 (AA 171-270) (Cy3) (ABIN1416263)
抗原
See all LHPP 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 171-270
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预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,Horse,Rabbit
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human HDHD2B/LHPP
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亚型
- IgG
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应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- LHPP (Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP))
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别名
- HDHD2B
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背景
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Synonyms: FLJ44846, FLJ46044, HDHD2B, hLHPP, lhpp, LHPP_HUMAN, Phospholysine phosphohistidine inorganic pyrophosphate phosphatase.
Background: 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.
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基因ID
- 64077
抗原
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