C7orf43 抗体 (AA 301-400)
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- 抗原 See all C7orf43 products
- C7orf43 (Chromosome 7 Open Reading Frame 43 (C7orf43))
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抗原表位
- AA 301-400
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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 C7orf43 antibody is un-conjugated
- 应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC)
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C7ORF43
- 亚型
- IgG
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anti-Chromosome 7 Open Reading Frame 43 (C7orf43) (AA 503-552) antibody
C7orf43 适用: 人, Cow, 豚鼠, 小鼠, 兔, 大鼠, 斑马鱼, Bat, 猴, Pig, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 7 Open Reading Frame 43 (C7orf43) (Middle Region) antibodyC7orf43 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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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
ICC 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
- 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
- C7orf43 (Chromosome 7 Open Reading Frame 43 (C7orf43))
- 别名
- C7ORF43 (C7orf43 产品)
- 别名
- chromosome 3 open reading frame, human C7orf43 antibody, chromosome 7 open reading frame 43 antibody, C3H7orf43 antibody, c7orf43 antibody, C7orf43 antibody
- 背景
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Synonyms: C7orf43, CG043_HUMAN, Chromosome 7 open reading frame 43, DKFZp761G0712, FLJ10925, Hypothetical protein LOC55262, Uncharacterized protein C7orf43.
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 C7orf43 gene product has been provisionally designated C7orf43 pending further characterization.
- 基因ID
- 55262
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