Cytochrome P450 11A1 Antibody - #DF4697

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产品: Cytochrome P450 11A1 抗体
货号: DF4697
描述: Rabbit polyclonal antibody to Cytochrome P450 11A1
应用: WB IHC IF/ICC
反应: Human, Mouse, Rat
预测: Bovine
分子量: 60 KD; 60kD(Calculated).
蛋白号: P05108
RRID: AB_2837048

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 50ul RMB¥ 1250 现货
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产品描述

来源:
Rabbit
应用:
WB 1:500-1:1000, IF/ICC 1:100-1:500, IHC 1:50-1:200
*The optimal dilutions should be determined by the end user.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human,Mouse,Rat
预测:
Bovine(86%)
克隆:
Polyclonal
特异性:
Cytochrome P450 11A1 Antibody detects endogenous levels of total Cytochrome P450 11A1.
RRID:
AB_2837048
引用格式: Affinity Biosciences Cat# DF4697, RRID:AB_2837048.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:

展开/折叠

Cholesterol 20 22 desmolase; Cholesterol desmolase; Cholesterol monooxygenase (side chain cleaving); Cholesterol side chain cleavage enzyme; Cholesterol side chain cleavage enzyme mitochondrial; Cholesterol side-chain cleavage enzyme; CP11A_HUMAN; CYP11A; CYP11A1; CYPXIA1; Cytochrome P450 11A1; Cytochrome P450 11A1 mitochondrial; Cytochrome P450 family 11 subfamily A polypeptide 1; Cytochrome P450 subfamily XIA; Cytochrome P450(scc); Cytochrome P450C11A1; mitochondrial; P450SCC; Steroid 20 22 lyase;

抗原和靶标

免疫原:
Uniprot:

P05108(CP11A_HUMAN) >>Visit HPA database.

基因/基因ID:
CYP11A1(1583)
序列:
MLAKGLPPRSVLVKGCQTFLSAPREGLGRLRVPTGEGAGISTRSPRPFNEIPSPGDNGWLNLYHFWRETGTHKVHLHHVQNFQKYGPIYREKLGNVESVYVIDPEDVALLFKSEGPNPERFLIPPWVAYHQYYQRPIGVLLKKSAAWKKDRVALNQEVMAPEATKNFLPLLDAVSRDFVSVLHRRIKKAGSGNYSGDISDDLFRFAFESITNVIFGERQGMLEEVVNPEAQRFIDAIYQMFHTSVPMLNLPPDLFRLFRTKTWKDHVAAWDVIFSKADIYTQNFYWELRQKGSVHHDYRGILYRLLGDSKMSFEDIKANVTEMLAGGVDTTSMTLQWHLYEMARNLKVQDMLRAEVLAARHQAQGDMATMLQLVPLLKASIKETLRLHPISVTLQRYLVNDLVLRDYMIPAKTLVQVAIYALGREPTFFFDPENFDPTRWLSKDKNITYFRNLGFGWGVRQCLGRRIAELEMTIFLINMLENFRVEIQHLSDVGTTFNLILMPEKPISFTFWPFNQEATQQ

种属预测

种属预测:

score>80的预测可信度较高，可尝试用于WB检测。*预测模型主要基于免疫原序列比对，结果仅作参考，不作为质保凭据。

Species
Results
Score
Bovine
86
Sheep
79
Dog
79
Rabbit
79
Horse
71
Chicken
70
Pig
64
Xenopus
60
Zebrafish
43
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

翻译修饰 - P05108 作为底物

Site PTM Type Enzyme
S113 Phosphorylation
T164 Phosphorylation

研究背景

功能:

A cytochrome P450 monooxygenase that catalyzes the side-chain hydroxylation and cleavage of cholesterol to pregnenolone, the precursor of most steroid hormones. Catalyzes three sequential oxidation reactions of cholesterol, namely the hydroxylation at C22 followed with the hydroxylation at C20 to yield 20R,22R-hydroxycholesterol that is further cleaved between C20 and C22 to yield the C21-steroid pregnenolone and 4-methylpentanal. Mechanistically, uses molecular oxygen inserting one oxygen atom into a substrate and reducing the second into a water molecule. Two electrons are provided by NADPH via a two-protein mitochondrial transfer system comprising flavoprotein FDXR (adrenodoxin/ferredoxin reductase) and nonheme iron-sulfur protein FDX1 or FDX2 (adrenodoxin/ferredoxin).

细胞定位:

Mitochondrion inner membrane>Peripheral membrane protein.
Note: Localizes to the matrix side of the mitochondrion inner membrane.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
亚基结构:

Interacts with FDX1/adrenodoxin.

蛋白家族:

Belongs to the cytochrome P450 family.

研究领域

· Metabolism > Lipid metabolism > Steroid hormone biosynthesis.

· Metabolism > Global and overview maps > Metabolic pathways.

· Organismal Systems > Endocrine system > Ovarian steroidogenesis.

· Organismal Systems > Endocrine system > Aldosterone synthesis and secretion.

文献引用

1). Interleukin 17A deficiency alleviates fluoride-induced testicular injury by inhibiting the immune response and apoptosis. Chemosphere, 2021 (PubMed: 33297146) [IF=8.8]

Application: WB    Species: Mice    Sample: testis

Fig. 5. IL-17A mediates the effect of excessive F on the testosterone level in serum and the expression of testosterone secretion-related proteins in testis (A) The content of testosterone in serum of mice (n ¼ 13. Three times repetition). (B) The expression of testosterone secretion-related proteins in testis (n ¼ 13. Three times repetition). Statistical analysis was carried out using one-way ANOVA with Dunnett’s test. Error bars denote the mean ± s.e.m. *P < 0.05, **P < 0.01.
2). The Curcumin Derivative, H10, Suppresses Hormone-Dependent Prostate Cancer by Inhibiting 17β-Hydroxysteroid Dehydrogenase Type 3. Frontiers in Pharmacology, 2020 (PubMed: 32457626) [IF=5.6]

Application: WB    Species: mouse    Sample: LC540 (17b-HSD3) cells

FIGURE 3 | Effects of H10 on 17b-HSD3 in LC540 (17b-HSD3) cells. Effects of H10 on the production of (A) T and (B) P. (C) The expression of 17b-HSD3 mRNA.(D) The expression levels of the proteins in the T synthesis pathway were detected by western blotting following treatment with H10. The concentrations of H10 were 0.25, 0.5, and 1 mM, while the concentration of 3858858 (positive control) was 0.25 mM.
3). Deubiquitinase UCHL1 regulates estradiol synthesis by stabilizing voltage-dependent anion channel 2. Journal of Biological Chemistry, 2023 (PubMed: 37797697) [IF=4.8]
4). Effects of high-intensity interval training on adipose tissue lipolysis, inflammation, and metabolomics in aged rats. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2020 (PubMed: 32006095) [IF=4.5]

Application: WB    Species: rat    Sample: fat

Fig. 4 |Metabolic pathway enrichment analysis and lipolysis metabolismrelated protein and mRNA expression. Correlation analysis of 9 metabolites (a); metabolic pathway analysis in MICT versus SED (b);mRNA levels of PPAR-γ, HSL, ATGL, and TNF-α in adipose tissues (c);correlation analysis of 6 metabolites (d); metabolic pathway analysis in HIIT versus SED (e); and contents of PPAR-γ, HSL, ATGL, TNF-α, and P450scc protein (f).
5). Quercetin Alleviated H2O2-Induced Apoptosis and Steroidogenic Impairment in Goat Luteinized Granulosa Cells. JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2020 (PubMed: 32410385) [IF=3.6]

Application: WB    Species: goat    Sample: granulosa cells

FIGURE 1 Identification of luteinized granulosa cells (GCs). A, The production of progesterone (P4) in goat GCs was enhanced in the forskolin group, compared with the fetal bovine serum (FBS) group. B‐G, The messenger RNA (mRNA) expressions of CYP19A1, CCND2, and PCNA decreased in the forskolin group, whereas there was an increase in the mRNA expressions of PTGFR, HSD3B, and StAR. The relative expression levels were normalized to GAPDH. H‐J, The expression of HSD3B and P450scc proteins increased in the forskolin group. Data are presented as mean ± SEM of three independent experiments. Different letters indicate significant differences (P < .05)
6). Effects of LPS on the accumulation of lipid droplets, proliferation, and steroidogenesis in goat luteinized granulosa cells. JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY, 2019 (PubMed: 30934154) [IF=3.6]

Application: WB    Species: goat    Sample: LGCs

FIGURE 5| Effect of LPS on the key regulators during steroidogenesis in goat LGCs. Cells were cultured as in the figure.A, Cells were processed to analyze the expressions of STAR, P450scc, 3β‐HSD,and CYP19A1 protein by Western blot analysis. α‐Tubulin was used as an internal control.
7). Suppression of Notch Signaling Stimulates Progesterone Synthesis by Enhancing the Expression of NR5A2 and NR2F2 in Porcine Granulosa Cells. Genes, 2020 (PubMed: 31978970) [IF=3.5]

Application: WB    Species: porcine    Sample: pGCs

Figure 4. |Effects of NR5A2 knockdown on progesterone biosynthesis. (D,E) protein expression of NR5A2, StAR, Cyp11a1, and HSD3B. Primary pGCs were transfected with NR5A2 siRNA (siNR5A2) or scramble siRNA (siNC). Six hours later, the medium was changed to fresh medium with DMSO or DAPT, followed by further culture for 48 h. * means significant difference at p < 0.05.

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