C6orf192 抗体 (AA 50-80) (Cy5)
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- 抗原 See all C6orf192 抗体
- C6orf192 (Chromosome 6 Open Reading Frame 192 (C6orf192))
- 抗原表位
- AA 50-80
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适用
- 人, 小鼠, 大鼠
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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 C6orf192 antibody is conjugated to Cy5
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C6orf192
- 亚型
- IgG
- Top Product
- Discover our top product C6orf192 Primary Antibody
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anti-Chromosome 6 Open Reading Frame 192 (C6orf192) (AA 50-80) antibody
C6orf192 适用: 人, 小鼠, 大鼠 WB, IF (p), IHC (p) 宿主: 兔 Polyclonal unconjugated
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- 应用备注
- IF(IHC-P) 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
- C6orf192 (Chromosome 6 Open Reading Frame 192 (C6orf192))
- 别名
- C6orf192 (C6orf192 产品)
- 别名
- C3H6orf192 antibody, SLC18B1 antibody, C6orf192 antibody, dJ55C23.6 antibody, 1110021L09Rik antibody, solute carrier family 18, subfamily B, member 1 antibody, solute carrier family 18 member B1 antibody, slc18b1 antibody, SLC18B1 antibody, Slc18b1 antibody
- 背景
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Synonyms: C6orf192, dJ55C23.6, MFS-type transporter SLC18B1, Solute carrier family 18 member B1, SLC18B1
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 C6orf192 gene product has been provisionally designated C6orf192 pending further characterization.
- 基因ID
- 116843
- UniProt
- Q6NT16
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