DHRSX 抗体 (AA 51-150) (Biotin)
Quick Overview for DHRSX 抗体 (AA 51-150) (Biotin) (ABIN1398145)
抗原
适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 51-150
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预测反应
- Human
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human DHRSX
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亚型
- IgG
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anti-Dehydrogenase/reductase (SDR Family) X-Linked (DHRSX) (AA 1-330) antibody
DHRSX 适用: 人 WB, IF 宿主: 小鼠 Polyclonal unconjugated
anti-Dehydrogenase/reductase (SDR Family) X-Linked (DHRSX) (AA 32-330) antibodyDHRSX 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Dehydrogenase/reductase (SDR Family) X-Linked (DHRSX) (AA 32-81) antibodyDHRSX 适用: 人, Cow WB 宿主: 兔 Polyclonal unconjugated
anti-Dehydrogenase/reductase (SDR Family) X-Linked (DHRSX) (C-Term) antibodyDHRSX 适用: 人, 犬 WB 宿主: 兔 Polyclonal unconjugated
anti-Dehydrogenase/reductase (SDR Family) X-Linked (DHRSX) (C-Term) antibodyDHRSX 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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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
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C for 12 months.
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有效期
- 12 months
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- DHRSX (Dehydrogenase/reductase (SDR Family) X-Linked (DHRSX))
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别名
- DHRSX
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背景
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Synonyms: DHRS5X, DHRSX, DHRSXY, CXorf11, Dehydrogenase/reductase SDR family X linked, Dehydrogenase/reductase SDR family member on chromosome X, DHRS5Y, DHRSX_HUMAN, DHRSY, RP11 325D5.2.
Background: DHRSX (dehydrogenase/reductase SDR family member on chromosome X) is a 330 amino acid protein belonging to the short-chain dehydrogenases/reductases (SDR) family. Widely expressed, DHRSX is an oxidoreductase that contains a coenzyme binding site and a substrate binding site, indicating a possible role in cellular metabolism. The gene that encodes DHRSX is located in the pseudoautosomal region 1 (PAR1) of X and Y chromosomes. The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of a X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unusual number and combination of sex chromosomes being inherited, including Turner's syndrome, Klinefelter's syndrome and Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.
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基因ID
- 207063
抗原
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