LHPP 抗体 (AA 171-270) (AbBy Fluor® 750)
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- 抗原 See all LHPP 抗体
- LHPP (Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP))
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抗原表位
- AA 171-270
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This LHPP antibody is conjugated to AbBy Fluor® 750
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human HDHD2B/LHPP
- 亚型
- IgG
- Top Product
- Discover our top product LHPP Primary Antibody
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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
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- LHPP (Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP))
- 别名
- HDHD2B (LHPP 产品)
- 别名
- HDHD2B antibody, 2310007H09Rik antibody, zgc:165670 antibody, phospholysine phosphohistidine inorganic pyrophosphate phosphatase antibody, haloacid dehalogenase-like hydrolase domain-containing protein 2 antibody, phospholysine phosphohistidine inorganic pyrophosphate phosphatase S homeolog antibody, LHPP antibody, LB_102 antibody, PSPPH_2719 antibody, LOC5569494 antibody, CpipJ_CPIJ005727 antibody, Lhpp antibody, lhpp.S antibody, lhpp antibody
- 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.
- 基因ID
- 64077
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