quick prep micro mrna purification kit Search Results


quick prep micro mrna purification kit  (Promega)
90
Promega quick prep micro mrna purification kit
Quick Prep Micro Mrna Purification Kit, 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/quick+prep+micro+mrna+purification+kit/quick+prep+micro+mrna+purification+kit/pm10984610-38-17-23
Average 90 stars, based on 1 article reviews
quick prep micro mrna purification kit - by Bioz Stars, 2026-08
90/100 stars
  Buy from Supplier
prep micro mrna purification kit  (Danaher Inc)
86
Danaher Inc prep micro mrna purification kit
Fig. 2. Time course of expression of platelet-derived growth factor (PDGF) A-chain <t>mRNA</t> in rat carotid artery after balloon injury. mRNA was extracted directly with oligo-dT-cellulose, and expression of PDGF A-chain mRNA was evaluated by reverse transcription and polymerase chain reaction of RNA from vessels before and 2, 6, 12, 24 h, and 7 days after balloon injury. 18S ribosomal RNA is included as an internal control. The ratio of the abundance of PDGF A-chain mRNA to that of 18S mRNA was evaluated by densitometric analysis. Data are the means of experiments carried out in duplicate.
Prep Micro Mrna Purification Kit, supplied by Danaher Inc, 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/quick+prep+micro+mrna+purification+kit/pm12504837-94-40-45
Average 86 stars, based on 1 article reviews
prep micro mrna purification kit - by Bioz Stars, 2026-08
86/100 stars
  Buy from Supplier

Image Search Results


Fig. 2. Time course of expression of platelet-derived growth factor (PDGF) A-chain mRNA in rat carotid artery after balloon injury. mRNA was extracted directly with oligo-dT-cellulose, and expression of PDGF A-chain mRNA was evaluated by reverse transcription and polymerase chain reaction of RNA from vessels before and 2, 6, 12, 24 h, and 7 days after balloon injury. 18S ribosomal RNA is included as an internal control. The ratio of the abundance of PDGF A-chain mRNA to that of 18S mRNA was evaluated by densitometric analysis. Data are the means of experiments carried out in duplicate.

Journal: Cardiovascular research

Article Title: Chimeric DNA-RNA hammerhead ribozyme targeting PDGF A-chain mRNA specifically inhibits neointima formation in rat carotid artery after balloon injury.

doi: 10.1016/s0008-6363(02)00607-7

Figure Lengend Snippet: Fig. 2. Time course of expression of platelet-derived growth factor (PDGF) A-chain mRNA in rat carotid artery after balloon injury. mRNA was extracted directly with oligo-dT-cellulose, and expression of PDGF A-chain mRNA was evaluated by reverse transcription and polymerase chain reaction of RNA from vessels before and 2, 6, 12, 24 h, and 7 days after balloon injury. 18S ribosomal RNA is included as an internal control. The ratio of the abundance of PDGF A-chain mRNA to that of 18S mRNA was evaluated by densitometric analysis. Data are the means of experiments carried out in duplicate.

Article Snippet: Membranes were then incubated RNase free phosphate-buffered saline (PBS). mRNA was with goat anti-mouse IgG for 1 h at room temperature, and extracted directly with oligo-dT-cellulose using the Quick then washed once with TBST for 15 min. and then four Prep Micro mRNA Purification Kit (Amersham Pharmacia times for 5 min.

Techniques: Expressing, Derivative Assay, Reverse Transcription, Polymerase Chain Reaction, Control

Fig. 5. Effect of chimeric DNA–RNA ribozyme specific for platelet-derived growth factor (PDGF) A-chain on expression of PDGF A-chain mRNA and PDGF-AA protein in carotid artery after balloon injury. Two or 5 mg of or mismatch ribozyme was incubated within the artery lumen for 10 min. (A) Expression of PDGF A-chain mRNA in the carotid artery 6 h after balloon injury. (B) Ratio of PDGF A-chain to 18S mRNA. Data are the mean6S.E.M. (n54). * P,0.01 vs. balloon injury without ribozyme:Ribozyme (2). (C) Expression of PDGF-AA protein in carotid artery 24 h after balloon injury. a-Tubulin is included and used as an internal control.

Journal: Cardiovascular research

Article Title: Chimeric DNA-RNA hammerhead ribozyme targeting PDGF A-chain mRNA specifically inhibits neointima formation in rat carotid artery after balloon injury.

doi: 10.1016/s0008-6363(02)00607-7

Figure Lengend Snippet: Fig. 5. Effect of chimeric DNA–RNA ribozyme specific for platelet-derived growth factor (PDGF) A-chain on expression of PDGF A-chain mRNA and PDGF-AA protein in carotid artery after balloon injury. Two or 5 mg of or mismatch ribozyme was incubated within the artery lumen for 10 min. (A) Expression of PDGF A-chain mRNA in the carotid artery 6 h after balloon injury. (B) Ratio of PDGF A-chain to 18S mRNA. Data are the mean6S.E.M. (n54). * P,0.01 vs. balloon injury without ribozyme:Ribozyme (2). (C) Expression of PDGF-AA protein in carotid artery 24 h after balloon injury. a-Tubulin is included and used as an internal control.

Article Snippet: Membranes were then incubated RNase free phosphate-buffered saline (PBS). mRNA was with goat anti-mouse IgG for 1 h at room temperature, and extracted directly with oligo-dT-cellulose using the Quick then washed once with TBST for 15 min. and then four Prep Micro mRNA Purification Kit (Amersham Pharmacia times for 5 min.

Techniques: Derivative Assay, Expressing, Incubation, Control