C6orf201 抗体 (AA 1-100) (Biotin)
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- 抗原 See all C6orf201 products
- C6orf201 (Chromosome 6 Open Reading Frame 201 (C6orf201))
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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 C6orf201 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 小鼠
- 预测反应
- Human
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C6orf201
- 亚型
- IgG
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IHC-F 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
- 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 for 12 months.
- 有效期
- 12 months
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- 抗原
- C6orf201 (Chromosome 6 Open Reading Frame 201 (C6orf201))
- 别名
- C6orf201 (C6orf201 产品)
- 别名
- dJ1013A10.5 antibody, chromosome 6 open reading frame 201 antibody, C6orf201 antibody
- 背景
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Synonyms: C6orf201, CF201_HUMAN, Chromosome 6 open reading frame 201, dJ1013A10.5, Hypothetical protein LOC404220, MGC87625, Protein MGC87625, Uncharacterized protein C6orf201.
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 C6orf201 gene product has been provisionally designated C6orf201 pending further characterization.
- 基因ID
- 404220
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