LHPP 抗体 (AA 6-270)
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Quick Overview for LHPP 抗体 (AA 6-270) (ABIN7875947)
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 6-270
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原理
- LHPP Antibody / Phospholysine phosphohistidine inorganic pyrophosphate phosphatase
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纯化方法
- Antigen affinity purified
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免疫原
- An E.coli-derived human recombinant protein (amino acids K6-K270) was used as the immunogen for the LHPP antibody.
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亚型
- IgG
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anti-Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP) antibody
LHPP 适用: 人, 小鼠, 大鼠 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP) (AA 1-270) antibodyLHPP 适用: 人 WB, IF 宿主: 兔 Polyclonal unconjugated
anti-Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP) (AA 84-116) antibodyLHPP 适用: 人 WB 宿主: 兔 Polyclonal RB55322 unconjugated
anti-Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP) (AA 1-270) antibodyLHPP 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP) (C-Term) antibodyLHPP 适用: 人, 小鼠, 大鼠, Cow, 兔, 豚鼠, 马, 猴, Pig WB 宿主: 兔 Polyclonal unconjugated
anti-Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP) (AA 179-228) antibodyLHPP 适用: 人, 小鼠, 大鼠, Cow, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the LHPP antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Lyophilized
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缓冲液
- 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water
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储存条件
- 4 °C,-20 °C
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储存方法
- After reconstitution, the LHPP antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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- LHPP (Phospholysine Phosphohistidine Inorganic Pyrophosphate Phosphatase (LHPP))
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别名
- LHPP
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背景
- 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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UniProt
- Q9H008
抗原
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