NSDHL 抗体 (Middle Region)
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- 抗原 See all NSDHL 抗体
- NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))
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抗原表位
- Middle Region
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适用
- 人, 大鼠, 小鼠, Pig, 兔, Cow, 犬, 斑马鱼, 豚鼠, 马
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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 NSDHL antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- RAVLGANDPE KNFLTTAIRP HGIFGPRDPQ LVPILIEAAR NGKMKFVIGN
- 预测反应
- Cow: 100%, Dog: 100%, Guinea Pig: 86%, Horse: 100%, Human: 100%, Mouse: 100%, Pig: 100%, Rabbit: 100%, Rat: 100%, Zebrafish: 100%
- 产品特性
- This is a rabbit polyclonal antibody against NSDHL. It was validated on Western Blot using a cell lysate as a positive control.
- 纯化方法
- Protein A purified
- 免疫原
- The immunogen is a synthetic peptide directed towards the middle region of human NSDHL
- Top Product
- Discover our top product NSDHL Primary Antibody
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- 应用备注
- Optimal working dilutions should be determined experimentally by the investigator.
- 说明
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Antigen size: 373 AA
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- Lot specific
- 缓冲液
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
- 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.
- 注意事项
- Avoid repeated freeze-thaw cycles.
- 储存条件
- -20 °C
- 储存方法
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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- 抗原
- NSDHL (NAD(P) Dependent Steroid Dehydrogenase-Like (NSDHL))
- 别名
- NSDHL (NSDHL 产品)
- 别名
- zgc:112474 antibody, H105E3 antibody, SDR31E1 antibody, XAP104 antibody, AI747449 antibody, Bpa antibody, Str antibody, NAD(P) dependent steroid dehydrogenase-like antibody, NAD(P) dependent steroid dehydrogenase-like L homeolog antibody, NSDHL antibody, nsdhl antibody, nsdhl.L antibody, Nsdhl antibody
- 背景
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NSDHL is localized in the endoplasmic reticulum and is involved in cholesterol biosynthesis. Mutations in NSDHL 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.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.
Alias Symbols: H105E3, XAP104, SDR31E1
Protein Interaction Partner: UBC, FUS, SUMO3,
Protein Size: 373 - 分子量
- 42 kDa
- 基因ID
- 50814
- NCBI登录号
- NM_015922, NP_057006
- UniProt
- Q15738
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