HEBP1 抗体 (Biotin)
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- 抗原 See all HEBP1 抗体
- HEBP1 (Heme Binding Protein 1 (HEBP1))
- 适用
- 人, 小鼠, 大鼠
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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 HEBP1 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human HEBP1/p22HBP
- 亚型
- IgG
- Top Product
- Discover our top product HEBP1 Primary Antibody
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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
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WB 1:300-5000
IHC-P 1:200-400 - 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- HEBP1 (Heme Binding Protein 1 (HEBP1))
- 别名
- HEBP1 (HEBP1 产品)
- 别名
- HEBP1 antibody, HBP antibody, HEBP antibody, Hebp antibody, heme binding protein 1 antibody, heme binding protein 1 L homeolog antibody, HEBP1 antibody, Hebp1 antibody, hebp1.L antibody
- 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.
- 基因ID
- 50865
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