SAYSD1 抗体 (AA 130-180) (Biotin)
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- 抗原 See all SAYSD1 products
- SAYSD1 (SAYSVFN Motif Domain Containing 1 (SAYSD1))
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抗原表位
- AA 130-180
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适用
- 人, 大鼠, 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 SAYSD1 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (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 C6orf64
- 亚型
- IgG
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400 - 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
- SAYSD1 (SAYSVFN Motif Domain Containing 1 (SAYSD1))
- 别名
- C6orf64 (SAYSD1 产品)
- 别名
- C6orf64 antibody, SAYSD1 antibody, C23H6orf64 antibody, 1810063B07Rik antibody, 4930488P03Rik antibody, SAYSVFN motif domain containing 1 antibody, SAYSD1 antibody, Saysd1 antibody
- 背景
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Synonyms: Chromosome 6 open reading frame 64, DKFZp434H012, FLJ11101, Hypothetical protein LOC55776, Uncharacterized protein C6orf64, SMDC1_HUMAN, SAYSD1, SAYSvFN domain-containing protein 1
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 C6orf64 gene product has been provisionally designated C6orf64 pending further characterization.
- 基因ID
- 55776
- UniProt
- Q9NPB0
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