5α dihydrotestosterone Search Results


91
TargetMol dihydrotestosterone
Dihydrotestosterone, supplied by TargetMol, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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steraloids inc dht
FIG. 1. Differential display PCR analysis. A, Human ZR-75–1 breast cancer cells were grown for 48 h in the presence <t>of</t> <t>estradiol</t> (10210 M) alone (control) or in combination with <t>DHT</t> (1029 M). Total RNA was isolated from control and DHT-treated cells and used for cDNA syn- thesis in the presence of oligo(dT) primer and Moloney murine leu- kemia virus reverse transcriptase. A fraction of each cDNA was am- plified by PCR using P4 and T1 primers, [a-33P]dATP, and dNTP mix. The products were analyzed on a denaturing 6% acrylamide gel. The gel was dried and exposed to x-ray film. B, The differentially displayed cDNA was amplified by PCR using the P4 and T1 primers and was separated on a 1% agarose gel along with DNA size markers.
Dht, supplied by steraloids inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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steraloids inc dihydrotestosterone
FIG. 1. Differential display PCR analysis. A, Human ZR-75–1 breast cancer cells were grown for 48 h in the presence <t>of</t> <t>estradiol</t> (10210 M) alone (control) or in combination with <t>DHT</t> (1029 M). Total RNA was isolated from control and DHT-treated cells and used for cDNA syn- thesis in the presence of oligo(dT) primer and Moloney murine leu- kemia virus reverse transcriptase. A fraction of each cDNA was am- plified by PCR using P4 and T1 primers, [a-33P]dATP, and dNTP mix. The products were analyzed on a denaturing 6% acrylamide gel. The gel was dried and exposed to x-ray film. B, The differentially displayed cDNA was amplified by PCR using the P4 and T1 primers and was separated on a 1% agarose gel along with DNA size markers.
Dihydrotestosterone, supplied by steraloids inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/5%CE%B1+dihydrotestosterone/5%CE%B1-ANDROSTAN-17%CE%B2-OL-3-ONE/bio_rxiv__2023__11__09__564741-211-0-4
Average 93 stars, based on 1 article reviews
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86
Millipore 5α dihydrotestosterone d3
FIG. 1. Differential display PCR analysis. A, Human ZR-75–1 breast cancer cells were grown for 48 h in the presence <t>of</t> <t>estradiol</t> (10210 M) alone (control) or in combination with <t>DHT</t> (1029 M). Total RNA was isolated from control and DHT-treated cells and used for cDNA syn- thesis in the presence of oligo(dT) primer and Moloney murine leu- kemia virus reverse transcriptase. A fraction of each cDNA was am- plified by PCR using P4 and T1 primers, [a-33P]dATP, and dNTP mix. The products were analyzed on a denaturing 6% acrylamide gel. The gel was dried and exposed to x-ray film. B, The differentially displayed cDNA was amplified by PCR using the P4 and T1 primers and was separated on a 1% agarose gel along with DNA size markers.
5α Dihydrotestosterone D3, supplied by Millipore, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/5%CE%B1+dihydrotestosterone/5alpha-Dihydrotestosterone-D3+(16%2C16%2C17-D3)+(0%2E1+mg%2Fml)+in+Methanol/pm30901160-51-0-30
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90
FUJIFILM 5α-dihydrotestosterone (dht
FIG. 1. Differential display PCR analysis. A, Human ZR-75–1 breast cancer cells were grown for 48 h in the presence <t>of</t> <t>estradiol</t> (10210 M) alone (control) or in combination with <t>DHT</t> (1029 M). Total RNA was isolated from control and DHT-treated cells and used for cDNA syn- thesis in the presence of oligo(dT) primer and Moloney murine leu- kemia virus reverse transcriptase. A fraction of each cDNA was am- plified by PCR using P4 and T1 primers, [a-33P]dATP, and dNTP mix. The products were analyzed on a denaturing 6% acrylamide gel. The gel was dried and exposed to x-ray film. B, The differentially displayed cDNA was amplified by PCR using the P4 and T1 primers and was separated on a 1% agarose gel along with DNA size markers.
5α Dihydrotestosterone (Dht, supplied by FUJIFILM, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/5%CE%B1+dihydrotestosterone/5%CE%B1+dihydrotestosterone++dht/pm19346694-39-22-24
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Dr Ehrenstorfer GmbH ar pathway agonist 5α-dihydrotestosterone (dht)
FIG. 1. Differential display PCR analysis. A, Human ZR-75–1 breast cancer cells were grown for 48 h in the presence <t>of</t> <t>estradiol</t> (10210 M) alone (control) or in combination with <t>DHT</t> (1029 M). Total RNA was isolated from control and DHT-treated cells and used for cDNA syn- thesis in the presence of oligo(dT) primer and Moloney murine leu- kemia virus reverse transcriptase. A fraction of each cDNA was am- plified by PCR using P4 and T1 primers, [a-33P]dATP, and dNTP mix. The products were analyzed on a denaturing 6% acrylamide gel. The gel was dried and exposed to x-ray film. B, The differentially displayed cDNA was amplified by PCR using the P4 and T1 primers and was separated on a 1% agarose gel along with DNA size markers.
Ar Pathway Agonist 5α Dihydrotestosterone (Dht), supplied by Dr Ehrenstorfer GmbH, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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DuPont de Nemours dht (5α-dihydrotestosterone)
FIG. 1. Differential display PCR analysis. A, Human ZR-75–1 breast cancer cells were grown for 48 h in the presence <t>of</t> <t>estradiol</t> (10210 M) alone (control) or in combination with <t>DHT</t> (1029 M). Total RNA was isolated from control and DHT-treated cells and used for cDNA syn- thesis in the presence of oligo(dT) primer and Moloney murine leu- kemia virus reverse transcriptase. A fraction of each cDNA was am- plified by PCR using P4 and T1 primers, [a-33P]dATP, and dNTP mix. The products were analyzed on a denaturing 6% acrylamide gel. The gel was dried and exposed to x-ray film. B, The differentially displayed cDNA was amplified by PCR using the P4 and T1 primers and was separated on a 1% agarose gel along with DNA size markers.
Dht (5α Dihydrotestosterone), supplied by DuPont de Nemours, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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NEN Life Science 14 c-labeled 5α-androstan-17 β -ol-3-one (dihydrotestosterone
FIG. 1. Differential display PCR analysis. A, Human ZR-75–1 breast cancer cells were grown for 48 h in the presence <t>of</t> <t>estradiol</t> (10210 M) alone (control) or in combination with <t>DHT</t> (1029 M). Total RNA was isolated from control and DHT-treated cells and used for cDNA syn- thesis in the presence of oligo(dT) primer and Moloney murine leu- kemia virus reverse transcriptase. A fraction of each cDNA was am- plified by PCR using P4 and T1 primers, [a-33P]dATP, and dNTP mix. The products were analyzed on a denaturing 6% acrylamide gel. The gel was dried and exposed to x-ray film. B, The differentially displayed cDNA was amplified by PCR using the P4 and T1 primers and was separated on a 1% agarose gel along with DNA size markers.
14 C Labeled 5α Androstan 17 β Ol 3 One (Dihydrotestosterone, supplied by NEN Life Science, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cambridge Isotope Laboratories 5α-dihydrotestosterone
Target analytes (19 steroid hormones), isotopically labeled internal standards, and their MRM parameters. MRM parameters include precursor ion (Q1), product ion (Q3), declustering potential (DP), entrance potential (EP), collision energy (CE), collision cell exit potential (CXP), and dwell time.
5α Dihydrotestosterone, supplied by Cambridge Isotope Laboratories, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/5%CE%B1+dihydrotestosterone/5%CE%B1+dihydrotestosterone/pmc09699436-139-20-93
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Merck KGaA 5α-dihydrotestosterone (dht)
Target analytes (19 steroid hormones), isotopically labeled internal standards, and their MRM parameters. MRM parameters include precursor ion (Q1), product ion (Q3), declustering potential (DP), entrance potential (EP), collision energy (CE), collision cell exit potential (CXP), and dwell time.
5α Dihydrotestosterone (Dht), supplied by Merck KGaA, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Toronto Research Chemicals d3 dihydrotestosterone
Target analytes (19 steroid hormones), isotopically labeled internal standards, and their MRM parameters. MRM parameters include precursor ion (Q1), product ion (Q3), declustering potential (DP), entrance potential (EP), collision energy (CE), collision cell exit potential (CXP), and dwell time.
D3 Dihydrotestosterone, supplied by Toronto Research Chemicals, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/5%CE%B1+dihydrotestosterone/Mestanolone-d3/pm22198065-57-17-19
Average 93 stars, based on 1 article reviews
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86
Macklin Inc 5α dihydrotestosterone
Target analytes (19 steroid hormones), isotopically labeled internal standards, and their MRM parameters. MRM parameters include precursor ion (Q1), product ion (Q3), declustering potential (DP), entrance potential (EP), collision energy (CE), collision cell exit potential (CXP), and dwell time.
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Image Search Results


FIG. 1. Differential display PCR analysis. A, Human ZR-75–1 breast cancer cells were grown for 48 h in the presence of estradiol (10210 M) alone (control) or in combination with DHT (1029 M). Total RNA was isolated from control and DHT-treated cells and used for cDNA syn- thesis in the presence of oligo(dT) primer and Moloney murine leu- kemia virus reverse transcriptase. A fraction of each cDNA was am- plified by PCR using P4 and T1 primers, [a-33P]dATP, and dNTP mix. The products were analyzed on a denaturing 6% acrylamide gel. The gel was dried and exposed to x-ray film. B, The differentially displayed cDNA was amplified by PCR using the P4 and T1 primers and was separated on a 1% agarose gel along with DNA size markers.

Journal: Endocrinology

Article Title: Identification and cloning of a novel androgen-responsive gene, uridine diphosphoglucose dehydrogenase, in human breast cancer cells.

doi: 10.1210/endo.140.10.7071

Figure Lengend Snippet: FIG. 1. Differential display PCR analysis. A, Human ZR-75–1 breast cancer cells were grown for 48 h in the presence of estradiol (10210 M) alone (control) or in combination with DHT (1029 M). Total RNA was isolated from control and DHT-treated cells and used for cDNA syn- thesis in the presence of oligo(dT) primer and Moloney murine leu- kemia virus reverse transcriptase. A fraction of each cDNA was am- plified by PCR using P4 and T1 primers, [a-33P]dATP, and dNTP mix. The products were analyzed on a denaturing 6% acrylamide gel. The gel was dried and exposed to x-ray film. B, The differentially displayed cDNA was amplified by PCR using the P4 and T1 primers and was separated on a 1% agarose gel along with DNA size markers.

Article Snippet: 17b-Estradiol (E2) and DHT were purchased from Steraloids (Wilton, NH).

Techniques: Control, Isolation, Virus, Reverse Transcription, Acrylamide Gel Assay, Amplification, Agarose Gel Electrophoresis

FIG. 2. Northern blot analysis of androgen-regulated mRNAs. Total RNA was isolated from ZR-75–1 cells grown for 48 h in the presence of estradiol (10210 M) alone (control) or in combination with DHT (1029

Journal: Endocrinology

Article Title: Identification and cloning of a novel androgen-responsive gene, uridine diphosphoglucose dehydrogenase, in human breast cancer cells.

doi: 10.1210/endo.140.10.7071

Figure Lengend Snippet: FIG. 2. Northern blot analysis of androgen-regulated mRNAs. Total RNA was isolated from ZR-75–1 cells grown for 48 h in the presence of estradiol (10210 M) alone (control) or in combination with DHT (1029

Article Snippet: 17b-Estradiol (E2) and DHT were purchased from Steraloids (Wilton, NH).

Techniques: Northern Blot, Isolation, Control

FIG. 6. Time course of DHT treatment on UDPGDH mRNA levels in ZR-75–1 cells. ZR-75–1 cells were grown for 0, 1, 6, 24, and 48 h in medium containing estradiol (10210 M) supplemented with DHT (1029

Journal: Endocrinology

Article Title: Identification and cloning of a novel androgen-responsive gene, uridine diphosphoglucose dehydrogenase, in human breast cancer cells.

doi: 10.1210/endo.140.10.7071

Figure Lengend Snippet: FIG. 6. Time course of DHT treatment on UDPGDH mRNA levels in ZR-75–1 cells. ZR-75–1 cells were grown for 0, 1, 6, 24, and 48 h in medium containing estradiol (10210 M) supplemented with DHT (1029

Article Snippet: 17b-Estradiol (E2) and DHT were purchased from Steraloids (Wilton, NH).

Techniques:

FIG. 7. Northern analysis of UDPGDH mRNA levels after DHT, cy- cloheximide, actinomycin D, and hydroxyflutamide treatment in ZR- 75–1 cells. ZR-75–1 cells were grown in medium containing estradiol (10210 M) supplemented with 1029 M DHT, DHT plus cycloheximide, DHT plus actinomycin D, and DHT plus hydroxyflutamide (3 3 1026

Journal: Endocrinology

Article Title: Identification and cloning of a novel androgen-responsive gene, uridine diphosphoglucose dehydrogenase, in human breast cancer cells.

doi: 10.1210/endo.140.10.7071

Figure Lengend Snippet: FIG. 7. Northern analysis of UDPGDH mRNA levels after DHT, cy- cloheximide, actinomycin D, and hydroxyflutamide treatment in ZR- 75–1 cells. ZR-75–1 cells were grown in medium containing estradiol (10210 M) supplemented with 1029 M DHT, DHT plus cycloheximide, DHT plus actinomycin D, and DHT plus hydroxyflutamide (3 3 1026

Article Snippet: 17b-Estradiol (E2) and DHT were purchased from Steraloids (Wilton, NH).

Techniques: Northern Blot

Target analytes (19 steroid hormones), isotopically labeled internal standards, and their MRM parameters. MRM parameters include precursor ion (Q1), product ion (Q3), declustering potential (DP), entrance potential (EP), collision energy (CE), collision cell exit potential (CXP), and dwell time.

Journal: Toxics

Article Title: Determination of 19 Steroid Hormones in Human Serum and Urine Using Liquid Chromatography-Tandem Mass Spectrometry

doi: 10.3390/toxics10110687

Figure Lengend Snippet: Target analytes (19 steroid hormones), isotopically labeled internal standards, and their MRM parameters. MRM parameters include precursor ion (Q1), product ion (Q3), declustering potential (DP), entrance potential (EP), collision energy (CE), collision cell exit potential (CXP), and dwell time.

Article Snippet: Individual certified stock solutions of cortisone, 11-deoxycortisol, aldosterone, corticosterone, progesterone, 17α-OH-progesterone, pregnenolone, estrone, estradiol, testosterone, dehydroepiandrosterone (DEHA), 5α-dihydrotestosterone, 17α-OH-pregnenolone, 11-dehydrocorticosterone, androstenediol, 13 C 3 -cortisone, 13 C 3 -cortisol, 13 C 3 -11-deoxycortisol, D 4 -aldosterone, D 4 -corticosterone, 13 C 3 -progesterone, 13 C 3 -17α-OH-progesterone, 13 C 2 -D 2 -pregnenolone, 13 C 3 -estrone, 13 C 2 -estradiol, 13 C 3 -estriol, 13 C 3 -testosterone, 13 C 3 -DEHA, 13 C 3 -5α-OH-dihydrotestosterone, and 13 C 2 -D 2 -17α-OH-pregnenolone (100 μg/mL) with purities of 95–98% were purchased from Cambridge Isotope Laboratories (Andover, MA, USA).

Techniques: Labeling

Method validation parameters for the analysis of 19 steroid hormones in human urine.

Journal: Toxics

Article Title: Determination of 19 Steroid Hormones in Human Serum and Urine Using Liquid Chromatography-Tandem Mass Spectrometry

doi: 10.3390/toxics10110687

Figure Lengend Snippet: Method validation parameters for the analysis of 19 steroid hormones in human urine.

Article Snippet: Individual certified stock solutions of cortisone, 11-deoxycortisol, aldosterone, corticosterone, progesterone, 17α-OH-progesterone, pregnenolone, estrone, estradiol, testosterone, dehydroepiandrosterone (DEHA), 5α-dihydrotestosterone, 17α-OH-pregnenolone, 11-dehydrocorticosterone, androstenediol, 13 C 3 -cortisone, 13 C 3 -cortisol, 13 C 3 -11-deoxycortisol, D 4 -aldosterone, D 4 -corticosterone, 13 C 3 -progesterone, 13 C 3 -17α-OH-progesterone, 13 C 2 -D 2 -pregnenolone, 13 C 3 -estrone, 13 C 2 -estradiol, 13 C 3 -estriol, 13 C 3 -testosterone, 13 C 3 -DEHA, 13 C 3 -5α-OH-dihydrotestosterone, and 13 C 2 -D 2 -17α-OH-pregnenolone (100 μg/mL) with purities of 95–98% were purchased from Cambridge Isotope Laboratories (Andover, MA, USA).

Techniques: Biomarker Discovery

Method validation parameters for the analysis of 19 steroid hormones in human serum.

Journal: Toxics

Article Title: Determination of 19 Steroid Hormones in Human Serum and Urine Using Liquid Chromatography-Tandem Mass Spectrometry

doi: 10.3390/toxics10110687

Figure Lengend Snippet: Method validation parameters for the analysis of 19 steroid hormones in human serum.

Article Snippet: Individual certified stock solutions of cortisone, 11-deoxycortisol, aldosterone, corticosterone, progesterone, 17α-OH-progesterone, pregnenolone, estrone, estradiol, testosterone, dehydroepiandrosterone (DEHA), 5α-dihydrotestosterone, 17α-OH-pregnenolone, 11-dehydrocorticosterone, androstenediol, 13 C 3 -cortisone, 13 C 3 -cortisol, 13 C 3 -11-deoxycortisol, D 4 -aldosterone, D 4 -corticosterone, 13 C 3 -progesterone, 13 C 3 -17α-OH-progesterone, 13 C 2 -D 2 -pregnenolone, 13 C 3 -estrone, 13 C 2 -estradiol, 13 C 3 -estriol, 13 C 3 -testosterone, 13 C 3 -DEHA, 13 C 3 -5α-OH-dihydrotestosterone, and 13 C 2 -D 2 -17α-OH-pregnenolone (100 μg/mL) with purities of 95–98% were purchased from Cambridge Isotope Laboratories (Andover, MA, USA).

Techniques: Biomarker Discovery

Steroid hormones measured in plasma Standard Reference Material (SRM1950) using the method developed in this study and compared to the certified reference values. Reference values were only available for cortisol, progesterone, and testosterone.

Journal: Toxics

Article Title: Determination of 19 Steroid Hormones in Human Serum and Urine Using Liquid Chromatography-Tandem Mass Spectrometry

doi: 10.3390/toxics10110687

Figure Lengend Snippet: Steroid hormones measured in plasma Standard Reference Material (SRM1950) using the method developed in this study and compared to the certified reference values. Reference values were only available for cortisol, progesterone, and testosterone.

Article Snippet: Individual certified stock solutions of cortisone, 11-deoxycortisol, aldosterone, corticosterone, progesterone, 17α-OH-progesterone, pregnenolone, estrone, estradiol, testosterone, dehydroepiandrosterone (DEHA), 5α-dihydrotestosterone, 17α-OH-pregnenolone, 11-dehydrocorticosterone, androstenediol, 13 C 3 -cortisone, 13 C 3 -cortisol, 13 C 3 -11-deoxycortisol, D 4 -aldosterone, D 4 -corticosterone, 13 C 3 -progesterone, 13 C 3 -17α-OH-progesterone, 13 C 2 -D 2 -pregnenolone, 13 C 3 -estrone, 13 C 2 -estradiol, 13 C 3 -estriol, 13 C 3 -testosterone, 13 C 3 -DEHA, 13 C 3 -5α-OH-dihydrotestosterone, and 13 C 2 -D 2 -17α-OH-pregnenolone (100 μg/mL) with purities of 95–98% were purchased from Cambridge Isotope Laboratories (Andover, MA, USA).

Techniques: Clinical Proteomics