super rna labeling kits Search Results


sp-6 rna polymerase reagent kits for synthesis of labelled and unlabelled rnas  (Promega)
90
Promega sp-6 rna polymerase reagent kits for synthesis of labelled and unlabelled rnas
CD437 regulation of chimeric rabbit β-globin-p21 WAF1/CIP1 mRNA . Two independent sublines derived from transfection of RGB-WAF (581-2004) plasmid [31.4(A4) and 31.4(C5)] or RBG plasmid [29.6(1) and 29.6(2)] were grown either in the absence (-) or presence (+) of 1 μM CD437 for 48 hours. Total <t>RNAs</t> were prepared and expression of RBG transcripts analyzed by northern blot hybridization as described . Levels <t>of</t> <t>RNA</t> loading in each lane were assessed by signals from hybridization with ribosomal phosphoprotein 36B4 cDNA
Sp 6 Rna Polymerase Reagent Kits For Synthesis Of Labelled And Unlabelled Rnas, 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/result/sp-6 rna polymerase reagent kits for synthesis of labelled and unlabelled rnas/product/Promega
Average 90 stars, based on 1 article reviews
sp-6 rna polymerase reagent kits for synthesis of labelled and unlabelled rnas - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
super total rna extraction kits with rnase-free dnasei  (Promega)
90
Promega super total rna extraction kits with rnase-free dnasei
CD437 regulation of chimeric rabbit β-globin-p21 WAF1/CIP1 mRNA . Two independent sublines derived from transfection of RGB-WAF (581-2004) plasmid [31.4(A4) and 31.4(C5)] or RBG plasmid [29.6(1) and 29.6(2)] were grown either in the absence (-) or presence (+) of 1 μM CD437 for 48 hours. Total <t>RNAs</t> were prepared and expression of RBG transcripts analyzed by northern blot hybridization as described . Levels <t>of</t> <t>RNA</t> loading in each lane were assessed by signals from hybridization with ribosomal phosphoprotein 36B4 cDNA
Super Total Rna Extraction Kits With Rnase Free Dnasei, 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/result/super total rna extraction kits with rnase-free dnasei/product/Promega
Average 90 stars, based on 1 article reviews
super total rna extraction kits with rnase-free dnasei - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier
35 s-utp and rna labeling kits  (Amersham Life Sciences Inc)
90
Amersham Life Sciences Inc 35 s-utp and rna labeling kits
CD437 regulation of chimeric rabbit β-globin-p21 WAF1/CIP1 mRNA . Two independent sublines derived from transfection of RGB-WAF (581-2004) plasmid [31.4(A4) and 31.4(C5)] or RBG plasmid [29.6(1) and 29.6(2)] were grown either in the absence (-) or presence (+) of 1 μM CD437 for 48 hours. Total <t>RNAs</t> were prepared and expression of RBG transcripts analyzed by northern blot hybridization as described . Levels <t>of</t> <t>RNA</t> loading in each lane were assessed by signals from hybridization with ribosomal phosphoprotein 36B4 cDNA
35 S Utp And Rna Labeling Kits, supplied by Amersham Life Sciences Inc, 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/result/35 s-utp and rna labeling kits/product/Amersham Life Sciences Inc
Average 90 stars, based on 1 article reviews
35 s-utp and rna labeling kits - by Bioz Stars, 2026-03
90/100 stars
  Buy from Supplier

Image Search Results


CD437 regulation of chimeric rabbit β-globin-p21 WAF1/CIP1 mRNA . Two independent sublines derived from transfection of RGB-WAF (581-2004) plasmid [31.4(A4) and 31.4(C5)] or RBG plasmid [29.6(1) and 29.6(2)] were grown either in the absence (-) or presence (+) of 1 μM CD437 for 48 hours. Total RNAs were prepared and expression of RBG transcripts analyzed by northern blot hybridization as described . Levels of RNA loading in each lane were assessed by signals from hybridization with ribosomal phosphoprotein 36B4 cDNA

Journal: Journal of Molecular Signaling

Article Title: Novel cis-trans interactions are involved in post-transcriptional regulation of cyclin-dependent kinase inhibitor p21 WAF1/CIP1 mRNA

doi: 10.1186/1750-2187-5-12

Figure Lengend Snippet: CD437 regulation of chimeric rabbit β-globin-p21 WAF1/CIP1 mRNA . Two independent sublines derived from transfection of RGB-WAF (581-2004) plasmid [31.4(A4) and 31.4(C5)] or RBG plasmid [29.6(1) and 29.6(2)] were grown either in the absence (-) or presence (+) of 1 μM CD437 for 48 hours. Total RNAs were prepared and expression of RBG transcripts analyzed by northern blot hybridization as described . Levels of RNA loading in each lane were assessed by signals from hybridization with ribosomal phosphoprotein 36B4 cDNA

Article Snippet: The T 7 , T 3 , and SP-6 RNA polymerase reagent kits for synthesis of labelled and unlabelled RNAs were purchased from Promega (Madison, WI).

Techniques: Derivative Assay, Transfection, Plasmid Preparation, Expressing, Northern Blot, Hybridization

Multiple cell cytoplasmic proteins bind to radiolabelled p21 WAF1/CIP1 3'-UTR and GADD45 5'-UTR sense strand riboprobes . Transcription and labeling of the indicated probes as well as the in vitro binding reactions were as described in the Methods. The probes utilized and treatment times with CD437 (hr) are indicated above each lane in the respective panels. The cytoplasmic protein extracts were prepared from untreated (lanes marked 0 hours) or CD437-treated MDA-MB-468 (panels A-C), MCF-7 (panel C) and HL-60R (panel C) cells. Panel A, the protein extracts in lanes 4-6 and11-13 were pre-incubated with 200-fold excess of the respective unlabeled probe RNAs, while the protein extracts in lane 7 were pre-incubated with 200-fold excess of the unlabeled 3'-UTR of c-myc RNA followed by incubation with the indicated labeled probe RNAs. Probe 14.2 RNA is loaded in lane 14. Panel B , the protein extracts in lanes 3 and 6 were pre-incubated with 200-fold excess of the respective unlabeled probe RNAs, while the protein extracts in lane 7 were pre-incubated with 200-fold excess of the unlabeled 3'-UTR of c-myc RNA followed by incubation with the indicated labeled probe RNAs. Panel C , lanes 6, 12 represent the labeled probe only. The approximate migration of molecular weight standards is marked on the left side of respective panel, while the * and ** on the right side of each panel denote locations of the putative 85 kD and 55 kD complexes, respectively.

Journal: Journal of Molecular Signaling

Article Title: Novel cis-trans interactions are involved in post-transcriptional regulation of cyclin-dependent kinase inhibitor p21 WAF1/CIP1 mRNA

doi: 10.1186/1750-2187-5-12

Figure Lengend Snippet: Multiple cell cytoplasmic proteins bind to radiolabelled p21 WAF1/CIP1 3'-UTR and GADD45 5'-UTR sense strand riboprobes . Transcription and labeling of the indicated probes as well as the in vitro binding reactions were as described in the Methods. The probes utilized and treatment times with CD437 (hr) are indicated above each lane in the respective panels. The cytoplasmic protein extracts were prepared from untreated (lanes marked 0 hours) or CD437-treated MDA-MB-468 (panels A-C), MCF-7 (panel C) and HL-60R (panel C) cells. Panel A, the protein extracts in lanes 4-6 and11-13 were pre-incubated with 200-fold excess of the respective unlabeled probe RNAs, while the protein extracts in lane 7 were pre-incubated with 200-fold excess of the unlabeled 3'-UTR of c-myc RNA followed by incubation with the indicated labeled probe RNAs. Probe 14.2 RNA is loaded in lane 14. Panel B , the protein extracts in lanes 3 and 6 were pre-incubated with 200-fold excess of the respective unlabeled probe RNAs, while the protein extracts in lane 7 were pre-incubated with 200-fold excess of the unlabeled 3'-UTR of c-myc RNA followed by incubation with the indicated labeled probe RNAs. Panel C , lanes 6, 12 represent the labeled probe only. The approximate migration of molecular weight standards is marked on the left side of respective panel, while the * and ** on the right side of each panel denote locations of the putative 85 kD and 55 kD complexes, respectively.

Article Snippet: The T 7 , T 3 , and SP-6 RNA polymerase reagent kits for synthesis of labelled and unlabelled RNAs were purchased from Promega (Madison, WI).

Techniques: Labeling, In Vitro, Binding Assay, Incubation, Migration, Molecular Weight