NSDHL Recombinant Monoclonal Antibody
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中文名称:NSDHL重组抗体
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货号:CSB-RA843829A0HU
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规格:¥1320
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图片:
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Western Blot
Positive WB detected in: HepG2 whole cell lysate, Hela whole cell lysate, PC-3 whole cell lysate, HEK293 whole cell lysate
All lanes: NSDHL antibody at 1:1000
Secondary
Goat polyclonal to rabbit IgG at 1/50000 dilution
Predicted band size: 42 kDa
Observed band size: 42 kDa -
IHC image of CSB-RA843829A0HU diluted at 1:100 and staining in paraffin-embedded human testis tissue performed on a Leica BondTM system. After dewaxing and hydration, antigen retrieval was mediated by high pressure in a citrate buffer (pH 6.0). Section was blocked with 10% normal goat serum 30min at RT. Then primary antibody (1% BSA) was incubated at 4°C overnight. The primary is detected by a Goat anti-rabbit polymer IgG labeled by HRP and visualized using 0.05% DAB.
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其他:
产品详情
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产品描述:CSB-RA843829A0HU NSDHL重组单克隆抗体是针对NAD(P)依赖性类固醇脱氢酶样蛋白(NSDHL)研发的高特异性检测工具。该靶标蛋白作为胆固醇生物合成途径中C-4固醇脱羧酶复合物的关键组分,参与羊毛甾醇向胆固醇转化的关键步骤,在细胞膜稳态维持和脂代谢调控中发挥重要作用。本抗体经多种实验验证,在Western Blot中可特异性识别内源性NSDHL蛋白,推荐工作浓度1:500-1:2000,显示清晰的检测信号且背景干扰低;在免疫组织化学应用中(推荐稀释度1:50-1:200)能准确呈现蛋白在组织样本中的亚细胞定位。其单克隆特性确保批次间高度一致性,适用于胆固醇代谢通路研究、脂质相关疾病模型构建及分子互作机制探索等科研领域,为研究胆固醇合成异常相关疾病的分子基础提供可靠工具。
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Uniprot No.:
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基因名:NSDHL
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别名:Sterol-4-alpha-carboxylate 3-dehydrogenase, decarboxylating (EC 1.1.1.170) (Protein H105e3), NSDHL, H105E3
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反应种属:Human
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免疫原:A synthesized peptide derived from human NSDHL
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免疫原种属:Homo sapiens (Human)
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标记方式:Non-conjugated
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克隆类型:Monoclonal
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抗体亚型:Rabbit IgG
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纯化方式:Affinity-chromatography
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克隆号:20F2
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浓度:It differs from different batches. Please contact us to confirm it.
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保存缓冲液:Rabbit IgG in phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
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产品提供形式:Liquid
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应用范围:ELISA, WB, IHC
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推荐稀释比:
Application Recommended Dilution WB 1:500-1:2000 IHC 1:50-1:200 -
Protocols:
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储存条件:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
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货期:Basically, we can dispatch the products out in 1-3 working days after receiving your orders. Delivery time maybe differs from different purchasing way or location, please kindly consult your local distributors for specific delivery time.
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用途:For Research Use Only. Not for use in diagnostic or therapeutic procedures.
相关产品
靶点详情
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功能:Catalyzes the NAD(P)(+)-dependent oxidative decarboxylation of the C4 methyl groups of 4-alpha-carboxysterols in post-squalene cholesterol biosynthesis. Plays also a role in the regulation of the endocytic trafficking of EGFR.
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基因功能参考文献:
- Here we present the case of a 9-year-old Chinese girl born with the typical clinical features of CHILD syndrome. Evaluation of the skin lesions confirmed the diagnosis and led to identification of a heterozygous point mutation in exon 8 of the NSDHL gene. PMID: 26459993
- Our findings expand the spectrum of mutations in NSDHL in CHILD syndrome, and indicate that large exon deletions may be not rare. PMID: 26014843
- A novel missense mutation in the NSDHL gene identified in a Lithuanian family by targeted next-generation sequencing causes CK syndrome. PMID: 25900314
- human NSDHL protein and mouse Nsdhl mRNA were expressed in tissues synthesizing cholesterol and steroids and in all peripheral tissues affected by CHILD or CK syndromes. PMID: 22113624
- found that males with intellectual disability in another reported family with an NSDHL mutation (c.1098 dup [p.Arg367SerfsX33]) have CKS PMID: 21129721
- The missense mutation of the NSDHL gene is detected in CHILD syndrome. PMID: 19906044
- Lethality of Nsdhl deficient mouse embryos is rescued by transgenic mice expressing human Nsdhl. PMID: 19880419
- NAD(P)H steroid dehydrogenase-like protein is localized to lipid droplets PMID: 12837764
- NSDHL, an enzyme involved in cholesterol synthesis, traffics through the Golgi and accumulates on ER membranes and on the surface of lipid droplets. PMID: 14506130
- microarray analysis of gene expression related to NSDHL sterol dehydrogenase in embryonic fibroblasts PMID: 15805545
- A novel missense mutation (R199H) in exon 6 of the NSDHL gene was identified in a small subset of sporadic verruciform xanthomas. PMID: 16230564
- NAD(P) dependent steroid dehydrogenase-like (NSDHL)-shRNA sequences were designed and tested for their effectiveness. PMID: 17498944
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相关疾病:Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD); CK syndrome (CKS)
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亚细胞定位:Endoplasmic reticulum membrane; Single-pass membrane protein. Lipid droplet.
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蛋白家族:3-beta-HSD family
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组织特异性:Brain, heart, liver, lung, kidney, skin and placenta.
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数据库链接:
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