CNBD2 抗体 (AA 21-120) (HRP)
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- 抗原 See all CNBD2 products
- CNBD2 (Cyclic Nucleotide Binding Domain Containing 2 (CNBD2))
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抗原表位
- AA 21-120
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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 CNBD2 antibody is conjugated to HRP
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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
- 人
- 预测反应
- Mouse,Rat,Dog,Cow,Sheep,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C20orf152
- 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.
- 注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
- 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
- CNBD2 (Cyclic Nucleotide Binding Domain Containing 2 (CNBD2))
- 别名
- C20orf152 (CNBD2 产品)
- 别名
- C20orf152 antibody, CNMPD1 antibody, dJ954P9.1 antibody, 4921517L17Rik antibody, 5430421B09Rik antibody, Cris antibody, cyclic nucleotide binding domain containing 2 antibody, CNBD2 antibody, Cnbd2 antibody
- 背景
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Synonyms: C20orf152, Chromosome 20 open reading frame 152, CT152_HUMAN, dJ954P9.1, RP5-954P9.1, Uncharacterized protein C20orf152, Uncharacterized protein C20orf152 homolog.
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 C20orf152 gene product has been provisionally designated C20orf152 pending further characterization.
- 基因ID
- 140894
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