C6orf168 抗体 (AA 221-320) (FITC)
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- 抗原 See all C6orf168 (FAXC) 抗体
- C6orf168 (FAXC) (Failed Axon Connections Homolog (Drosophila) (FAXC))
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抗原表位
- AA 221-320
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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 C6orf168 antibody is conjugated to FITC
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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,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C6orf168
- 亚型
- IgG
- Top Product
- Discover our top product FAXC Primary Antibody
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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
- C6orf168 (FAXC) (Failed Axon Connections Homolog (Drosophila) (FAXC))
- 别名
- C6orf168 (FAXC 产品)
- 别名
- C6orf168 antibody, dJ273F20 antibody, failed axon connections homolog antibody, FAXC antibody
- 背景
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Synonyms: C6orf168, CF168_HUMAN, Chromosome 6 open reading frame 168, dJ273F20, Uncharacterized protein C6orf168.
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 C6orf168 gene product has been provisionally designated C6orf168 pending further characterization.
- 基因ID
- 84553
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