NSDHL 抗体
Quick Overview for NSDHL 抗体 (ABIN7465357)
抗原
See all NSDHL 抗体适用
宿主
克隆类型
标记
应用范围
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交叉反应
- 人
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纯化方法
- Purified by antigen-affinity chromatography.
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免疫原
- Recombinant protein encompassing a sequence within the center region of human NSDHL. The exact sequence is proprietary.
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亚型
- IgG
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anti-NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL) (AA 1-110) antibody
NSDHL 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 6E3 unconjugated
anti-NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL) (AA 1-240) antibodyKO Validated NSDHL 适用: 人 WB, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL) (AA 154-211) antibodyNSDHL 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL) (AA 1-373) antibodyNSDHL 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL) (AA 1-373) antibodyNSDHL 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL) (AA 181-230) antibodyNSDHL 适用: 人, 大鼠, 小鼠, Cow, 犬, 豚鼠, 马, Pig, 兔, 斑马鱼, Bat, 小鸡, 猴, 非洲爪蟾 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
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说明
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Positive Control: A431
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
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储存液
- Thimerosal (Merthiolate)
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注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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储存条件
- 4 °C,-20 °C
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储存方法
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))
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别名
- NAD(P) dependent steroid dehydrogenase-like
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背景
- NAD(P) dependent steroid dehydrogenase-like , H105E3 , SDR31E1 , XAP104,The protein encoded by this gene is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in this gene are associated with CHILD syndrome, which is a X-linked dominant disorder of lipid metabolism with disturbed cholesterol biosynthesis, and typically lethal in males. Alternatively spliced transcript variants with differing 5' UTR have been found for this gene. [provided by RefSeq]
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分子量
- 42 kDa
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基因ID
- 50814
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UniProt
- Q15738
抗原
-
