cdna ends Search Results


smart rapid amplification cdna ends (race) cdna amplification  (Becton Dickinson)
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Becton Dickinson smart rapid amplification cdna ends (race) cdna amplification
Smart Rapid Amplification Cdna Ends (Race) Cdna Amplification, supplied by Becton Dickinson, 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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smart rapid amplification cdna ends (race) cdna amplification - by Bioz Stars, 2026-08
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rapid amplification cdna ends (race  (GenScript corporation)
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GenScript corporation rapid amplification cdna ends (race
Rapid Amplification Cdna Ends (Race, supplied by GenScript corporation, 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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rapid amplification cdna ends (race - by Bioz Stars, 2026-08
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massive analysis of cdna ends (mace) libraries  (GenXPro Inc)
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GenXPro Inc massive analysis of cdna ends (mace) libraries
Massive Analysis Of Cdna Ends (Mace) Libraries, supplied by GenXPro Inc, 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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5’- 3’-race (rapid amplification cdna ends  (Becton Dickinson)
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Becton Dickinson 5’- 3’-race (rapid amplification cdna ends
5’ 3’ Race (Rapid Amplification Cdna Ends, supplied by Becton Dickinson, 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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5’- 3’-race (rapid amplification cdna ends - by Bioz Stars, 2026-08
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5′-rapid amplification of cdna ends  (SynGap Research Fund Inc)
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SynGap Research Fund Inc 5′-rapid amplification of cdna ends
5′ Rapid Amplification Of Cdna Ends, supplied by SynGap Research Fund Inc, 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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5’ rapid amplification cdna ends  (Oxford Nanopore)
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Oxford Nanopore 5’ rapid amplification cdna ends
5’ Rapid Amplification Cdna Ends, supplied by Oxford Nanopore, 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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3′ rapid amplification of cdna ends (3′race) cdna amplification kit  (Meridian Bioscience)
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Meridian Bioscience 3′ rapid amplification of cdna ends (3′race) cdna amplification kit
3′ Rapid Amplification Of Cdna Ends (3′Race) Cdna Amplification Kit, supplied by Meridian Bioscience, 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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3′ rapid amplification of cdna ends (3′race) cdna amplification kit - by Bioz Stars, 2026-08
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5 -rapid amplification cdna ends (race) kit  (Becton Dickinson)
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Becton Dickinson 5 -rapid amplification cdna ends (race) kit
5 Rapid Amplification Cdna Ends (Race) Kit, supplied by Becton Dickinson, 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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rna ligase-mediated rapid amplification cdna ends (rlm–race  (Promega)
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Promega rna ligase-mediated rapid amplification cdna ends (rlm–race
Stimulation <t>of</t> <t>transcription</t> and expression of αE by transforming growth factor-β (TGF-β). (a) TK1 cells were treated for 16 hr with TGF-β and <t>RNA</t> was extracted at specific time-points and tested for αE transcripts. Probing for glyceraldehyde phosphate dehydrogenase (GAPDH) verified equal loading. (b) Cell-surface expression of αEβ7 by TK1 cells before (left panel) or after (right panel) treatment for 16 hr with TGF-β; black profiles show staining with monoclonal antibody (mAb) M290 (specific for αE), unfilled profiles show the negative control with isotyped-matched irrelevant mAb. (c) Nuclear run-on analysis to test for newly synthesized, nascent, αE transcripts in TK1 cells before and after treatment with TGF-β. 32P-labelled nuclear RNA was extracted from TK1 cells before or after overnight stimulation with TGF-β and from αE+ MTC-1 cells cultured in the presence of TGF-β. The RNA was tested for hybridization to αE cDNA. Detection of nascent mRNA for β-actin in all samples validated the technique.
Rna Ligase Mediated Rapid Amplification Cdna Ends (Rlm–Race, supplied by Promega, 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/cdna+ends/pmc01783235-147-7-15?v=Promega
Average 90 stars, based on 1 article reviews
rna ligase-mediated rapid amplification cdna ends (rlm–race - by Bioz Stars, 2026-08
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cdna ends amplification (race  (Becton Dickinson)
90
Becton Dickinson cdna ends amplification (race
Stimulation <t>of</t> <t>transcription</t> and expression of αE by transforming growth factor-β (TGF-β). (a) TK1 cells were treated for 16 hr with TGF-β and <t>RNA</t> was extracted at specific time-points and tested for αE transcripts. Probing for glyceraldehyde phosphate dehydrogenase (GAPDH) verified equal loading. (b) Cell-surface expression of αEβ7 by TK1 cells before (left panel) or after (right panel) treatment for 16 hr with TGF-β; black profiles show staining with monoclonal antibody (mAb) M290 (specific for αE), unfilled profiles show the negative control with isotyped-matched irrelevant mAb. (c) Nuclear run-on analysis to test for newly synthesized, nascent, αE transcripts in TK1 cells before and after treatment with TGF-β. 32P-labelled nuclear RNA was extracted from TK1 cells before or after overnight stimulation with TGF-β and from αE+ MTC-1 cells cultured in the presence of TGF-β. The RNA was tested for hybridization to αE cDNA. Detection of nascent mRNA for β-actin in all samples validated the technique.
Cdna Ends Amplification (Race, supplied by Becton Dickinson, 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/cdna+ends/us10041132-1010-7-10?v=Becton+Dickinson
Average 90 stars, based on 1 article reviews
cdna ends amplification (race - by Bioz Stars, 2026-08
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rapid amplification of cdna ends  (5 PRIME)
90
5 PRIME rapid amplification of cdna ends
Stimulation <t>of</t> <t>transcription</t> and expression of αE by transforming growth factor-β (TGF-β). (a) TK1 cells were treated for 16 hr with TGF-β and <t>RNA</t> was extracted at specific time-points and tested for αE transcripts. Probing for glyceraldehyde phosphate dehydrogenase (GAPDH) verified equal loading. (b) Cell-surface expression of αEβ7 by TK1 cells before (left panel) or after (right panel) treatment for 16 hr with TGF-β; black profiles show staining with monoclonal antibody (mAb) M290 (specific for αE), unfilled profiles show the negative control with isotyped-matched irrelevant mAb. (c) Nuclear run-on analysis to test for newly synthesized, nascent, αE transcripts in TK1 cells before and after treatment with TGF-β. 32P-labelled nuclear RNA was extracted from TK1 cells before or after overnight stimulation with TGF-β and from αE+ MTC-1 cells cultured in the presence of TGF-β. The RNA was tested for hybridization to αE cDNA. Detection of nascent mRNA for β-actin in all samples validated the technique.
Rapid Amplification Of Cdna Ends, supplied by 5 PRIME, 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/cdna+ends/pm25090642-103-23-19?v=5+PRIME
Average 90 stars, based on 1 article reviews
rapid amplification of cdna ends - by Bioz Stars, 2026-08
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rna ligase-mediated rapid amplification of cdna ends rlm–race  (Promega)
90
Promega rna ligase-mediated rapid amplification of cdna ends rlm–race
Stimulation <t>of</t> <t>transcription</t> and expression of αE by transforming growth factor-β (TGF-β). (a) TK1 cells were treated for 16 hr with TGF-β and RNA was extracted at specific time-points and tested for αE transcripts. Probing for glyceraldehyde phosphate dehydrogenase (GAPDH) verified equal loading. (b) Cell-surface expression of αEβ7 by TK1 cells before (left panel) or after (right panel) treatment for 16 hr with TGF-β; black profiles show staining with monoclonal antibody (mAb) M290 (specific for αE), unfilled profiles show the negative control with isotyped-matched irrelevant mAb. (c) Nuclear run-on analysis to test for newly synthesized, nascent, αE transcripts in TK1 cells before and after treatment with TGF-β. 32P-labelled nuclear RNA was extracted from TK1 cells before or after overnight stimulation with TGF-β and from αE+ MTC-1 cells cultured in the presence of TGF-β. The RNA was tested for hybridization to αE <t>cDNA.</t> Detection of nascent mRNA for β-actin in all samples validated the technique.
Rna Ligase Mediated Rapid Amplification Of Cdna Ends Rlm–Race, supplied by Promega, 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/cdna+ends/pmc01783235-147-12-15?v=Promega
Average 90 stars, based on 1 article reviews
rna ligase-mediated rapid amplification of cdna ends rlm–race - by Bioz Stars, 2026-08
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Image Search Results


Stimulation of transcription and expression of αE by transforming growth factor-β (TGF-β). (a) TK1 cells were treated for 16 hr with TGF-β and RNA was extracted at specific time-points and tested for αE transcripts. Probing for glyceraldehyde phosphate dehydrogenase (GAPDH) verified equal loading. (b) Cell-surface expression of αEβ7 by TK1 cells before (left panel) or after (right panel) treatment for 16 hr with TGF-β; black profiles show staining with monoclonal antibody (mAb) M290 (specific for αE), unfilled profiles show the negative control with isotyped-matched irrelevant mAb. (c) Nuclear run-on analysis to test for newly synthesized, nascent, αE transcripts in TK1 cells before and after treatment with TGF-β. 32P-labelled nuclear RNA was extracted from TK1 cells before or after overnight stimulation with TGF-β and from αE+ MTC-1 cells cultured in the presence of TGF-β. The RNA was tested for hybridization to αE cDNA. Detection of nascent mRNA for β-actin in all samples validated the technique.

Journal:

Article Title: Studies on transcriptional regulation of the mucosal T-cell integrin ?E?7 (CD103)

doi: 10.1046/j.1365-2567.2001.01232.x

Figure Lengend Snippet: Stimulation of transcription and expression of αE by transforming growth factor-β (TGF-β). (a) TK1 cells were treated for 16 hr with TGF-β and RNA was extracted at specific time-points and tested for αE transcripts. Probing for glyceraldehyde phosphate dehydrogenase (GAPDH) verified equal loading. (b) Cell-surface expression of αEβ7 by TK1 cells before (left panel) or after (right panel) treatment for 16 hr with TGF-β; black profiles show staining with monoclonal antibody (mAb) M290 (specific for αE), unfilled profiles show the negative control with isotyped-matched irrelevant mAb. (c) Nuclear run-on analysis to test for newly synthesized, nascent, αE transcripts in TK1 cells before and after treatment with TGF-β. 32P-labelled nuclear RNA was extracted from TK1 cells before or after overnight stimulation with TGF-β and from αE+ MTC-1 cells cultured in the presence of TGF-β. The RNA was tested for hybridization to αE cDNA. Detection of nascent mRNA for β-actin in all samples validated the technique.

Article Snippet: The transcription start sites were identified by RNA Ligase-Mediated Rapid Amplification of cDNA Ends (RLM–RACE; Promega UK Ltd, Southampton, UK), according to the supplier's protocol.

Techniques: Expressing, Staining, Negative Control, Synthesized, Cell Culture, Hybridization

Stimulation of transcription and expression of αE by transforming growth factor-β (TGF-β). (a) TK1 cells were treated for 16 hr with TGF-β and RNA was extracted at specific time-points and tested for αE transcripts. Probing for glyceraldehyde phosphate dehydrogenase (GAPDH) verified equal loading. (b) Cell-surface expression of αEβ7 by TK1 cells before (left panel) or after (right panel) treatment for 16 hr with TGF-β; black profiles show staining with monoclonal antibody (mAb) M290 (specific for αE), unfilled profiles show the negative control with isotyped-matched irrelevant mAb. (c) Nuclear run-on analysis to test for newly synthesized, nascent, αE transcripts in TK1 cells before and after treatment with TGF-β. 32P-labelled nuclear RNA was extracted from TK1 cells before or after overnight stimulation with TGF-β and from αE+ MTC-1 cells cultured in the presence of TGF-β. The RNA was tested for hybridization to αE cDNA. Detection of nascent mRNA for β-actin in all samples validated the technique.

Journal:

Article Title: Studies on transcriptional regulation of the mucosal T-cell integrin ?E?7 (CD103)

doi: 10.1046/j.1365-2567.2001.01232.x

Figure Lengend Snippet: Stimulation of transcription and expression of αE by transforming growth factor-β (TGF-β). (a) TK1 cells were treated for 16 hr with TGF-β and RNA was extracted at specific time-points and tested for αE transcripts. Probing for glyceraldehyde phosphate dehydrogenase (GAPDH) verified equal loading. (b) Cell-surface expression of αEβ7 by TK1 cells before (left panel) or after (right panel) treatment for 16 hr with TGF-β; black profiles show staining with monoclonal antibody (mAb) M290 (specific for αE), unfilled profiles show the negative control with isotyped-matched irrelevant mAb. (c) Nuclear run-on analysis to test for newly synthesized, nascent, αE transcripts in TK1 cells before and after treatment with TGF-β. 32P-labelled nuclear RNA was extracted from TK1 cells before or after overnight stimulation with TGF-β and from αE+ MTC-1 cells cultured in the presence of TGF-β. The RNA was tested for hybridization to αE cDNA. Detection of nascent mRNA for β-actin in all samples validated the technique.

Article Snippet: The transcription start sites were identified by RNA Ligase-Mediated Rapid Amplification of cDNA Ends (RLM–RACE; Promega UK Ltd, Southampton, UK), according to the supplier's protocol.

Techniques: Expressing, Staining, Negative Control, Synthesized, Cell Culture, Hybridization