DHRS13 抗体 (Cy3)
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- 抗原 See all DHRS13 抗体
- DHRS13 (Dehydrogenase/reductase (SDR Family) Member 13 (DHRS13))
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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 DHRS13 antibody is conjugated to Cy3
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应用范围
- Western Blotting (WB)
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Cow,Sheep,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human DHRS13
- 亚型
- IgG
- Top Product
- Discover our top product DHRS13 Primary Antibody
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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
- Sodium azide
- 注意事项
- This product contains Sodium azide: 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
- DHRS13 (Dehydrogenase/reductase (SDR Family) Member 13 (DHRS13))
- 别名
- Dhrs13 (DHRS13 产品)
- 别名
- 2610209N15Rik antibody, SDR7C5 antibody, RGD1305508 antibody, dhrs13 antibody, zgc:91936 antibody, dehydrogenase/reductase (SDR family) member 13 antibody, dehydrogenase/reductase 13 antibody, dehydrogenase/reductase (SDR family) member 13 L homeolog antibody, dehydrogenase/reductase (SDR family) member 13b antibody, Dhrs13 antibody, DHRS13 antibody, dhrs13.L antibody, dhrs13b antibody
- 背景
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Synonyms: Dehydrogenase/reductase SDR family member 13, Dehydrogenase/reductase SDR family member 13, DHRS 13, MGC23280, OTTHUMP00000163522, SDR7C5, Short chain dehydrogenase/reductase family 7C member 5, DHR13_HUMAN.
Background: DHRS13 (dehydrogenase/reductase SDR family member 13), also known as UNQ419/PRO853, is a 377 amino acid secreted protein belonging to the short-chain dehydrogenases/reductases (SDR) family. DHRS13 is presumed to function as an oxidoreductase and is phosphorylated, potentially by ATM or ATR, upon DNA damage. DHRS13 exists as two isoforms produced by alternative splicing events. The gene encoding DHRS13 maps to human chromosome 17, which comprises over 2.5 % of the human genome and encodes over 1,200 genes. Neurofibromatosis, dysregulated Schwann cell growth, Alexander disease, Birt-Hogg-Dube syndrome and Canavan disease are associated with chromosome 17.
- 基因ID
- 147015
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