C20orf43 抗体 (HRP)
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- 抗原 See all C20orf43 抗体
- C20orf43 (Chromosome 20 Open Reading Frame 43 (C20orf43))
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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 C20orf43 antibody is conjugated to HRP
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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 C20orf43
- 亚型
- IgG
- Top Product
- Discover our top product C20orf43 Primary Antibody
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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.
- 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
- C20orf43 (Chromosome 20 Open Reading Frame 43 (C20orf43))
- 别名
- C20orf43 (C20orf43 产品)
- 别名
- C20orf43 antibody, C17H20orf43 antibody, CDAO5 antibody, HSPC164 antibody, SHUJUN-3 antibody, C13H20orf43 antibody, RGD1311072 antibody, 1700067C04Rik antibody, 2410001C21Rik antibody, 5730427M17Rik antibody, AA589417 antibody, replication termination factor 2 domain containing 1 antibody, RTFDC1 antibody, Rtfdc1 antibody
- 背景
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Synonyms: C20orf43, CDAO5, chromosome 20 open reading frame 43, CT043_HUMAN, HSPC164, Hypothetical protein LOC51507, SHUJUN-3, UPF0549 protein C20orf43.
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 C20orf43 gene product has been provisionally designated C20orf43 pending further characterization.
- 基因ID
- 51507
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