NSDHL 抗体
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北京 101111
Quick Overview for NSDHL 抗体 (ABIN6989853)
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, 大鼠
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纯化方法
- Purified by Protein A.
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免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-240 of human NSDHL (NP_057006.1).
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亚型
- IgG
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anti-NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL) antibody
KD Validated NSDHL 适用: 人 WB, ICC, FACS 宿主: 兔 Monoclonal 24GB485 unconjugated Recombinant Antibody
anti-NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL) antibodyKD Validated NSDHL 适用: 人 WB, ICC, FACS 宿主: 兔 Monoclonal 24GB510 unconjugated Recombinant Antibody
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 1-110) antibodyNSDHL 适用: 人 WB, ELISA 宿主: 小鼠 Monoclonal 6E3 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
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WB 1:300-5000
IF(ICC) 1:50-200
IF() -
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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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- NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))
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别名
- NSDHL
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背景
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Synonyms: NSDHL,H105E3,SDR31E1,XAP104
Background: 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.
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基因ID
- 50814
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UniProt
- Q15738
抗原
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