C6ORF62 抗体 (AA 1-100) (AbBy Fluor® 350)
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- 抗原 See all C6ORF62 products
- C6ORF62 (Chromosome 6 Open Reading Frame 62 (C6ORF62))
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抗原表位
- AA 1-100
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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
- This C6ORF62 antibody is conjugated to AbBy Fluor® 350
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Cow,Sheep,Chicken,Rabbit,Hamster
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C6orf62
- 亚型
- IgG
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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
- C6ORF62 (Chromosome 6 Open Reading Frame 62 (C6ORF62))
- 别名
- C6orf62 (C6ORF62 产品)
- 别名
- Nbla00237 antibody, XTP12 antibody, dJ30M3.2 antibody, C6orf62 antibody, 8030460C05Rik antibody, C78201 antibody, chromosome 6 open reading frame 62 antibody, chromosome 2 open reading frame, human C6orf62 antibody, cDNA sequence BC005537 antibody, chromosome 6 open reading frame, human C6orf62 antibody, chromosome 23 open reading frame, human C6orf62 antibody, C6orf62 antibody, C2H6ORF62 antibody, BC005537 antibody, C6H6orf62 antibody, C23H6orf62 antibody
- 背景
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Synonyms: C6orf62, CF062_HUMAN, HBV X-transactivated gene 12 protein, HBV XAg-transactivated protein 12, Nbla00237, Uncharacterized protein C6orf62, XTP12.
Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf62 gene product has been provisionally designated C6orf62 pending further characterization.
- 基因ID
- 81688
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