C7orf10 抗体 (AA 351-445) (Cy3)
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- 抗原 See all C7orf10 抗体
- C7orf10 (Chromosome 7 Open Reading Frame 10 (C7orf10))
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抗原表位
- AA 351-445
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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 C7orf10 antibody is conjugated to Cy3
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (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 C7orf10
- 亚型
- IgG
- Top Product
- Discover our top product C7orf10 Primary Antibody
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anti-Chromosome 7 Open Reading Frame 10 (C7orf10) (AA 335-434) antibody
C7orf10 适用: 人 ELISA 宿主: 小鼠 Monoclonal 2B11 unconjugated
anti-Chromosome 7 Open Reading Frame 10 (C7orf10) (AA 1-471) antibodyC7orf10 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Chromosome 7 Open Reading Frame 10 (C7orf10) (AA 104-153) antibodyC7orf10 适用: 人, 小鼠, 兔, Cow, 豚鼠, 马, 猴, Pig, Bat WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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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
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- C7orf10 (Chromosome 7 Open Reading Frame 10 (C7orf10))
- 别名
- C7orf10 (C7orf10 产品)
- 别名
- DERP13 antibody, ORF19 antibody, c7orf10 antibody, sugct antibody, succinyl-CoA:glutarate-CoA transferase antibody, succinyl-CoA:glutarate-CoA transferase L homeolog antibody, SUGCT antibody, sugct.L antibody
- 背景
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Synonyms: Chromosome 7 open reading frame 10, Dermal papilla derived protein 13, DERP13, FLJ11808, Hypothetical protein LOC79783, ORF19, Russel-Silver syndrome candidate, Uncharacterized protein C7orf10,CG010_HUMAN.
Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf10 gene product has been provisionally designated C7orf10 pending further characterization.
- 基因ID
- 79783
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