C6ORF195 抗体 (AA 81-127) (Alexa Fluor 594)
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- 抗原 See all C6ORF195 products
- C6ORF195 (Chromosome 6 Open Reading Frame 195 (C6ORF195))
- 抗原表位
- AA 81-127
- 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 C6ORF195 antibody is conjugated to Alexa Fluor 594
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应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C6orf195
- 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
- C6ORF195 (Chromosome 6 Open Reading Frame 195 (C6ORF195))
- 别名
- C6orf195 (C6ORF195 产品)
- 别名
- RP11-145H9.2 antibody, bA145H9.2 antibody, long intergenic non-protein coding RNA 1600 antibody, LINC01600 antibody
- 背景
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Synonyms: bA145H9.2, C6orf195, CF195_HUMAN, Chromosome 6 open reading frame 195, FLJ31934, RP11-145H9.2, Uncharacterized protein C6orf195.
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 C6orf195 gene product has been provisionally designated C6orf195 pending further characterization.
- 基因ID
- 154386
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