C7ORF26 抗体 (AA 1-100)
C7ORF26
适用: 人
WB, IF (cc), IF (p), ELISA, IHC (fro), IHC (p), ICC
宿主: 兔
Polyclonal
unconjugated
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- 抗原 See all C7ORF26 products
- C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))
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抗原表位
- AA 1-100
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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 C7ORF26 antibody is un-conjugated
- 应用范围
- Western Blotting (WB), 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,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C7orf26
- 亚型
- IgG
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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
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
- C7ORF26 (Chromosome 7 Open Reading Frame 26 (C7ORF26))
- 别名
- C7orf26 (C7ORF26 产品)
- 别名
- C14H7orf26 antibody, zgc:77458 antibody, c7orf26 antibody, chromosome 7 open reading frame 26 antibody, chromosome 14 C7orf26 homolog antibody, zgc:56409 antibody, chromosome 7 open reading frame 26 L homeolog antibody, chromosome 25 open reading frame, human C7orf26 antibody, C7orf26 antibody, C14H7orf26 antibody, zgc:56409 antibody, c7orf26.L antibody, C25H7orf26 antibody
- 背景
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Synonyms: Chromosome 7 open reading frame 26, MGC2718, Uncharacterized protein C7orf26,CG026_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 C7orf26 gene product has been provisionally designated C7orf26 pending further characterization.
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