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Anti-CYP17A1 Antibody (4G627) 是一种抗体,靶向 CYP17A1。Anti-CYP17A1 Antibody (4G627) 可用于 ELISA, WB, IHC, IF。
Anti-CYP17A1 Antibody (4G627) 是一种抗体,靶向 CYP17A1。Anti-CYP17A1 Antibody (4G627) 可用于 ELISA, WB, IHC, IF。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
50 μL | ¥ 1,305 | 5日内发货 | |
100 μL | ¥ 2,180 | 5日内发货 |
产品描述 | Anti-CYP17A1 Antibody (4G627) is an antibody targeting CYP17A1. Anti-CYP17A1 Antibody (4G627) can be used in ELISA, WB, IHC, IF. |
Ig Type | Rabbit IgG |
克隆号 | 4G627 |
交叉反应 | Human, Rat |
验证活性 | 1. Western Blot -Positive WB detected in: HepG2 whole cell lysate, Rat Heart whole cell lysate, Rat Brain whole cell lysate -All lanes: CYP17A1 antibody at 1:1000 -Secondary: Goat polyclonal to rabbit IgG at 1/50000 dilution -Predicted band size: 58 kDa -Observed band size: 58 kDa 2. IHC image of TMAH-00326 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 IgG polymer labeled by HRP and visualized using 0.05% DAB. 3. Immunofluorescence staining of Hela Cells with TMAH-00326 at 1:50, counter-stained with DAPI. The cells were fixed in 4% formaldehyde, permeated by 0.2% TritonX-100, and blocked in 10% normal Goat Serum. The cells were then incubated with the antibody overnight at 4°C. Nuclear DNA was labeled in blue with DAPI. The secondary antibody was FITC-conjugated AffiniPure Goat Anti-Rabbit IgG (H+L). |
应用 | ELISA, WB, IHC, IF |
推荐剂量 | WB:1:500-1:5000; IHC:1:50-1:200; IF:1:20-1:200. |
抗体种类 | Monoclonal |
亚细胞定位 | Endoplasmic reticulum membrane. Microsome membrane. |
构建方式 | Recombinant Antibody |
纯化方式 | Affinity-chromatography |
性状 | Liquid |
缓冲液 | Phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. |
研究背景 | A cytochrome P450 monooxygenase involved in corticoid and androgen biosynthesis. Catalyzes 17-alpha hydroxylation of C21 steroids, which is common for both pathways. A second oxidative step, required only for androgen synthesis, involves an acyl-carbon cleavage. The 17-alpha hydroxy intermediates, as part of adrenal glucocorticoids biosynthesis pathway, are precursors of cortisol (Probable). Hydroxylates steroid hormones, pregnenolone and progesterone to form 17-alpha hydroxy metabolites, followed by the cleavage of the C17-C20 bond to form C19 steroids, dehydroepiandrosterone (DHEA) and androstenedione. Has 16-alpha hydroxylase activity. Catalyzes 16-alpha hydroxylation of 17-alpha hydroxy pregnenolone, followed by the cleavage of the C17-C20 bond to form 16-alpha-hydroxy DHEA. Also 16-alpha hydroxylates androgens, relevant for estriol synthesis. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate, and reducing the second into a water molecule, with two electrons provided by NADPH via cytochrome P450 reductase (CPR; NADPH-ferrihemoprotein reductase). |
偶联 | Unconjugated |
免疫原 | A synthetic peptide: Human Cytochrome P450 17A1 |
抗原种属 | Human |
基因ID | 1586 |
Uniprot ID | |
研究领域 | Cancer, Cardiovascular, Metabolism, Signal transduction |
储存方式 | Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. |
运输方式 | Shipping with blue ice. |
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