RFESD 抗体 (AA 51-157) (Biotin)
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- 抗原 See all RFESD products
- RFESD (Rieske (Fe-S) Domain Containing (RFESD))
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抗原表位
- AA 51-157
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适用
- 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 RFESD antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 交叉反应
- 大鼠
- 预测反应
- Human,Mouse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human RFESD
- 亚型
- IgG
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anti-Rieske (Fe-S) Domain Containing (RFESD) (AA 1-157) antibody
RFESD 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Rieske (Fe-S) Domain Containing (RFESD) (AA 35-84) antibodyRFESD 适用: 人, 小鼠, 豚鼠, 马, Pig, Bat, Hamster 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
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
- RFESD (Rieske (Fe-S) Domain Containing (RFESD))
- 别名
- RFESD (RFESD 产品)
- 别名
- MGC82457 antibody, zgc:112118 antibody, AI256775 antibody, D030068K09 antibody, RGD1308284 antibody, Rieske Fe-S domain containing antibody, Rieske (Fe-S) domain containing L homeolog antibody, Rieske (Fe-S) domain containing antibody, RFESD antibody, rfesd.L antibody, rfesd antibody, Rfesd antibody
- 背景
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Synonyms: Rieske Fe S domain containing, Rieske domain containing protein, RFESD_HUMAN.
Background: RFESD, also known as Rieske domain-containing protein, is a 157 amino acid protein that binds one 2Fe-2S cluster per subunit. Involved in metal ion binding, RFESD contains one Rieske domain. The RFESD gene is conserved in chimpanzee, dog, cow, mouse, rat, chicken and zebrafish, and maps to human chromosome 5q15. Chromosome 5 makes up approximately 6 % of the human genome and contains 181 million base pairs, which encode 1,000 genes. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is caused by insertions or deletions within the TCOF1 gene and is also associated with chromosome 5. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
- 基因ID
- 317671
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