OR10A5 抗体 (AA 231-317) (Biotin)
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- 抗原 See all OR10A5 抗体
- OR10A5 (Olfactory Receptor, Family 10, Subfamily A, Member 5 (OR10A5))
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抗原表位
- AA 231-317
- 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 OR10A5 antibody is conjugated to Biotin
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应用范围
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human OR10A5
- 亚型
- IgG
- Top Product
- Discover our top product OR10A5 Primary Antibody
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- 应用备注
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IHC-P 1:200-400
IHC-F 1:100-500 - 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
- OR10A5 (Olfactory Receptor, Family 10, Subfamily A, Member 5 (OR10A5))
- 别名
- OR10A5 (OR10A5 产品)
- 别名
- JCG6 antibody, OR10A1 antibody, OR11-403 antibody, olfactory receptor family 10 subfamily A member 5 antibody, olfactory receptor antibody, OR10A5 antibody, OR10B10 antibody
- 背景
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Synonyms: HP3, O10A5_HUMAN, Olfactory receptor 10A1, Olfactory receptor 10A5, Olfactory receptor 11-403, Olfactory receptor-like protein JCG6, OR10A1, OR10A5, OR11-403, R10A1.
Background: Olfactory receptors interact with odorant molecules in the nose to initiate a neuronal response that leads to the perception of smell. While they share a seven transmembrane domain structure with many neurotransmitter and hormone receptors, olfactory receptors are responsible for the recognition and transduction of odorant signals. OR10A2 (olfactory receptor 10A2) and OR10A5 (olfactory receptor 10A5) are multi-pass membrane proteins that belong to the G-protein coupled receptor 1 family and are encoded by genes that map to human chromosome 11p15.4. Chromosome 11 houses over 1,400 genes and comprises nearly 4 % of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that map to chromosome 11.
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