Cytochrome b5 (CYTB5) (AA 9-80) 抗体
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- 抗原 See all Cytochrome b5 (CYTB5) 抗体
- Cytochrome b5 (CYTB5)
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抗原表位
- AA 9-80
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适用
- 小鼠
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- 非结合性
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应用范围
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Dog,Cow,Sheep,Pig
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Cytochrome b5
- 亚型
- IgG
- Top Product
- Discover our top product CYTB5 Primary Antibody
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- Cytochrome b5 (CYTB5)
- 别名
- Cytochrome b5 (CYTB5 产品)
- 别名
- CYB5 antibody, MCB5 antibody, Cyb5 antibody, 0610009N12Rik antibody, Cyb5a antibody, CYB5A antibody, 1857 antibody, BcDNA:GH02503 antibody, BcDNA:RE66521 antibody, CG2140 antibody, CYT-B5 antibody, CYTB5 antibody, Dmel\\CG2140 antibody, dpld antibody, l(2)01857 antibody, l(2)k00107 antibody, cytochrome b5 type A antibody, cytochrome b5 type A (microsomal) antibody, cytochrome b5 antibody, Cytochrome b5 antibody, CYB5A antibody, Cyb5a antibody, LOC100328915 antibody, LOC100735904 antibody, Cyt-b5 antibody
- 背景
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Synonyms: CYB 5, CYB 5A, CYB5, CYB5_HUMAN, CYB5A, Cytochrome b 5, Cytochrome b5 microsomal, Cytochrome b5, Cytochrome b5 type A microsomal, Cytochrome b5 type A, MCB 5, MCB5, Microsomal cytochrome b5, Microsomal cytochrome b5 type A, Type 1 cyt b5, CYB5A.
Background: The protein encoded by this gene is a membrane-bound cytochrome that reduces ferric hemoglobin (methemoglobin) to ferrous hemoglobin, which is required for stearyl-CoA-desaturase activity. Defects in this gene are a cause of type IV hereditary methemoglobinemia. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2010]
- 基因ID
- 1528
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