SCP2D1 抗体 (AA 101-156) (Cy7)
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- 抗原 See all SCP2D1 抗体
- SCP2D1 (SCP2 Sterol-Binding Domain Containing 1 (SCP2D1))
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抗原表位
- AA 101-156
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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 SCP2D1 antibody is conjugated to Cy7
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Dog,Cow,Sheep,Pig,Horse,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C20orf79
- 亚型
- IgG
- Top Product
- Discover our top product SCP2D1 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
- SCP2D1 (SCP2 Sterol-Binding Domain Containing 1 (SCP2D1))
- 别名
- C20orf79 (SCP2D1 产品)
- 别名
- C20orf79 antibody, HSD22 antibody, dJ1068E13.2 antibody, C13H20orf79 antibody, 1700010M22Rik antibody, SCP2 sterol binding domain containing 1 antibody, SCP2 sterol-binding domain containing 1 antibody, SCP2D1 antibody, Scp2d1 antibody
- 背景
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Synonyms: Chromosome 20 open reading frame 79, dJ1068E13.2, HSD22, Hypothetical protein LOC140856, MGC138229, OTTHUMP00000030367, Sterol carrier protein 2 like protein, Uncharacterized protein C20orf79.
Background: Representing about 2 % of human DNA, chromosome 20 consists of approximately 63 million bases and 600 genes. Chromosome 20 contains a region with numerous genes expressed in the epididymis, which are thought important for seminal production, and some viewed as potential targets for male contraception. The PRNP gene encoding the prion protein associated with spongiform encephalopathies, like Creutzfeldt-Jakob disease, is found on chromosome 20. Amyotrophic lateral sclerosis, spinal muscular atrophy, ring chromosome 20 epilepsy syndrome and Alagille syndrome are also associated with chromosome 20. The C20orf79 gene product has been provisionally designated C20orf79 pending further characterization.
- 基因ID
- 140856
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