44330 Search Results


92
ATCC p boydii
P Boydii, supplied by ATCC, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ATCC pseudallescheria boydii
Pseudallescheria Boydii, supplied by ATCC, 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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93
Santa Cruz Biotechnology rna sirna duplex targeting yy1
CP-31398-mediated augmentation of p21 and suppression of <t>YY1</t> expression. Esophageal carcinoma cells treated with CP-31398 (A) at different concentrations as indicated for 48 hrs or (B) at 10 μM for different times as indicated, were subjected to Western blot analysis. Actin was used as a loading control.
Rna Sirna Duplex Targeting Yy1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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91
Cell Signaling Technology Inc gap43
CP-31398-mediated augmentation of p21 and suppression of <t>YY1</t> expression. Esophageal carcinoma cells treated with CP-31398 (A) at different concentrations as indicated for 48 hrs or (B) at 10 μM for different times as indicated, were subjected to Western blot analysis. Actin was used as a loading control.
Gap43, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/gap43/product/Cell Signaling Technology Inc
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93
Addgene inc vector plasmid pzac2 1 gfaabc1d lck gcamp3
CP-31398-mediated augmentation of p21 and suppression of <t>YY1</t> expression. Esophageal carcinoma cells treated with CP-31398 (A) at different concentrations as indicated for 48 hrs or (B) at 10 μM for different times as indicated, were subjected to Western blot analysis. Actin was used as a loading control.
Vector Plasmid Pzac2 1 Gfaabc1d Lck Gcamp3, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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86
DSMZ tsukamurella tyrosinosolvens
Figure 1. Findings of DNA-DNA homology studies with solid-phase dot-blot hybridizations for <t>Tsukamurella</t> species. Probe and target DNAs are indicated. Strain numbers beginning with “A” are from the American Type Culture Collection system.
Tsukamurella Tyrosinosolvens, supplied by DSMZ, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Santa Cruz Biotechnology shrna targeting yy1
Figure 1. Findings of DNA-DNA homology studies with solid-phase dot-blot hybridizations for <t>Tsukamurella</t> species. Probe and target DNAs are indicated. Strain numbers beginning with “A” are from the American Type Culture Collection system.
Shrna Targeting Yy1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Celestron International imaging system celestron model 44330
Figure 1. Findings of DNA-DNA homology studies with solid-phase dot-blot hybridizations for <t>Tsukamurella</t> species. Probe and target DNAs are indicated. Strain numbers beginning with “A” are from the American Type Culture Collection system.
Imaging System Celestron Model 44330, supplied by Celestron International, 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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Celestron International imaging system celestron 44330
Figure 1. Findings of DNA-DNA homology studies with solid-phase dot-blot hybridizations for <t>Tsukamurella</t> species. Probe and target DNAs are indicated. Strain numbers beginning with “A” are from the American Type Culture Collection system.
Imaging System Celestron 44330, supplied by Celestron International, 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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Image Search Results


CP-31398-mediated augmentation of p21 and suppression of YY1 expression. Esophageal carcinoma cells treated with CP-31398 (A) at different concentrations as indicated for 48 hrs or (B) at 10 μM for different times as indicated, were subjected to Western blot analysis. Actin was used as a loading control.

Journal: American Journal of Cancer Research

Article Title: A p53-stabilizing agent, CP-31398, induces p21 expression with increased G2/M phase through the YY1 transcription factor in esophageal carcinoma defective of the p53 pathway

doi:

Figure Lengend Snippet: CP-31398-mediated augmentation of p21 and suppression of YY1 expression. Esophageal carcinoma cells treated with CP-31398 (A) at different concentrations as indicated for 48 hrs or (B) at 10 μM for different times as indicated, were subjected to Western blot analysis. Actin was used as a loading control.

Article Snippet: Cells were transfected with small interfering RNA (siRNA) duplex targeting YY1 (#sc-36863), p21 (#sc-29427) (Santa Cruz Biotechnology, Santa Cruz, CA, USA), p53 (#TP53-VHS40367) or with non-coding siRNA (#12935-114) as a control (Thermo Fisher Scientific, Fremont, CA, USA) using Lipofectamine RNAiMAX according to the manufacturer’s protocol (Thermo Fisher Scientific).

Techniques: Expressing, Western Blot, Control

CP-31398-mediated up-regulation of p21 was independent of p53 but associated with YY1 expression. (A) Esophageal carcinoma cells treated with CP-31398 as indicated for 48 hrs and amounts of p21 transcripts were analyzed with RT-PCR. GAPDH transcripts are shown as a control. (B, C) Cells transfected with either (B) p53-siRNA or (C) YY1-siRNA were treated with CP-31398 at 10 μM for 48 hrs and subjected to Western blot analysis. Cells transfected with control siRNA were also used as a reference. Actin was used as a loading control.

Journal: American Journal of Cancer Research

Article Title: A p53-stabilizing agent, CP-31398, induces p21 expression with increased G2/M phase through the YY1 transcription factor in esophageal carcinoma defective of the p53 pathway

doi:

Figure Lengend Snippet: CP-31398-mediated up-regulation of p21 was independent of p53 but associated with YY1 expression. (A) Esophageal carcinoma cells treated with CP-31398 as indicated for 48 hrs and amounts of p21 transcripts were analyzed with RT-PCR. GAPDH transcripts are shown as a control. (B, C) Cells transfected with either (B) p53-siRNA or (C) YY1-siRNA were treated with CP-31398 at 10 μM for 48 hrs and subjected to Western blot analysis. Cells transfected with control siRNA were also used as a reference. Actin was used as a loading control.

Article Snippet: Cells were transfected with small interfering RNA (siRNA) duplex targeting YY1 (#sc-36863), p21 (#sc-29427) (Santa Cruz Biotechnology, Santa Cruz, CA, USA), p53 (#TP53-VHS40367) or with non-coding siRNA (#12935-114) as a control (Thermo Fisher Scientific, Fremont, CA, USA) using Lipofectamine RNAiMAX according to the manufacturer’s protocol (Thermo Fisher Scientific).

Techniques: Expressing, Reverse Transcription Polymerase Chain Reaction, Control, Transfection, Western Blot

CP-31398-mediated cell cycle changes were attributable to augmented p21 expression. A. Cells transfected with p21-siRNA or control siRNA were treated with CP-31398 at 10 μM for 48 hrs and subjected to Western blot analysis. Actin was used as a loading control. B. Representative cell cycle profiles of cells treated with siRNA and/or CP-31398 at 10 μM for 48 hrs. The profiles were examined with a flow cytometry. A percentage of each fraction was shown in Table 2.

Journal: American Journal of Cancer Research

Article Title: A p53-stabilizing agent, CP-31398, induces p21 expression with increased G2/M phase through the YY1 transcription factor in esophageal carcinoma defective of the p53 pathway

doi:

Figure Lengend Snippet: CP-31398-mediated cell cycle changes were attributable to augmented p21 expression. A. Cells transfected with p21-siRNA or control siRNA were treated with CP-31398 at 10 μM for 48 hrs and subjected to Western blot analysis. Actin was used as a loading control. B. Representative cell cycle profiles of cells treated with siRNA and/or CP-31398 at 10 μM for 48 hrs. The profiles were examined with a flow cytometry. A percentage of each fraction was shown in Table 2.

Article Snippet: Cells were transfected with small interfering RNA (siRNA) duplex targeting YY1 (#sc-36863), p21 (#sc-29427) (Santa Cruz Biotechnology, Santa Cruz, CA, USA), p53 (#TP53-VHS40367) or with non-coding siRNA (#12935-114) as a control (Thermo Fisher Scientific, Fremont, CA, USA) using Lipofectamine RNAiMAX according to the manufacturer’s protocol (Thermo Fisher Scientific).

Techniques: Expressing, Transfection, Control, Western Blot, Flow Cytometry

Cell cycle progression of esophageal carcinoma cells which were treated with CP-31398 and  siRNA

Journal: American Journal of Cancer Research

Article Title: A p53-stabilizing agent, CP-31398, induces p21 expression with increased G2/M phase through the YY1 transcription factor in esophageal carcinoma defective of the p53 pathway

doi:

Figure Lengend Snippet: Cell cycle progression of esophageal carcinoma cells which were treated with CP-31398 and siRNA

Article Snippet: Cells were transfected with small interfering RNA (siRNA) duplex targeting YY1 (#sc-36863), p21 (#sc-29427) (Santa Cruz Biotechnology, Santa Cruz, CA, USA), p53 (#TP53-VHS40367) or with non-coding siRNA (#12935-114) as a control (Thermo Fisher Scientific, Fremont, CA, USA) using Lipofectamine RNAiMAX according to the manufacturer’s protocol (Thermo Fisher Scientific).

Techniques: Control

Figure 1. Findings of DNA-DNA homology studies with solid-phase dot-blot hybridizations for Tsukamurella species. Probe and target DNAs are indicated. Strain numbers beginning with “A” are from the American Type Culture Collection system.

Journal: Clinical infectious diseases : an official publication of the Infectious Diseases Society of America

Article Title: Central venous catheter-related bacteremia due to Tsukamurella species in the immunocompromised host: a case series and review of the literature.

doi: 10.1086/342561

Figure Lengend Snippet: Figure 1. Findings of DNA-DNA homology studies with solid-phase dot-blot hybridizations for Tsukamurella species. Probe and target DNAs are indicated. Strain numbers beginning with “A” are from the American Type Culture Collection system.

Article Snippet: The type strain of Tsukamurella tyrosinosolvens (DSM 44234) was purchased from the Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH.

Techniques: Dot Blot