HEBP1 抗体 (AbBy Fluor® 647)
Quick Overview for HEBP1 抗体 (AbBy Fluor® 647) (ABIN1405248)
抗原
See all HEBP1 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人, 小鼠, 大鼠
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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 HEBP1/p22HBP
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亚型
- IgG
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anti-Heme Binding Protein 1 (HEBP1) antibody
HEBP1 适用: 人 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Heme Binding Protein 1 (HEBP1) (AA 80-189) antibodyHEBP1 适用: 人 WB, ELISA 宿主: 小鼠 Polyclonal unconjugated
anti-Heme Binding Protein 1 (HEBP1) (AA 1-189) antibodyHEBP1 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Heme Binding Protein 1 (HEBP1) (AA 1-171) antibodyHEBP1 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- IF(IHC-P) 1:50-200
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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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- HEBP1 (Heme Binding Protein 1 (HEBP1))
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别名
- HEBP1
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背景
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Synonyms: HBP, HEBP, Hebp1, HEBP1_HUMAN, Heme binding protein 1, Heme-binding protein 1, p22HBP.
Background: p22HBP, also known as HEBP1 (heme binding protein 1), HBP or HEBP, is a 189 amino acid intracellular tetrapyrrole-binding protein that assists in prevention of cellular toxicity by removing free porphyrinogens from the cell. Existing as a monomer, p22HBP localizes to cytoplasm and contains a 21 amino acid chemoattractant within its N-terminus that functions as a natural ligand for FPR3. p22HBP is a member of the HEBP family and binds N-methylprotoporphyrin and metalloporphyrins with similar affinity to porphyrinogens. The gene encoding p22HBP maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
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基因ID
- 50865
抗原
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