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Bio-Rad semi quantitative rt pcr cdna
Regulation of M. smegmatis adenylate cyclase genes under starvation conditions. Semi-quantitative <t>RT-PCR</t> was used to compare adenylate cyclase mRNA levels between late-log phase cultures incubated for 4 h in mycomedia (control) or PBS (starvation). (A) A representative depiction of PCR-amplified <t>cDNA</t> separated using agarose gel electrophoresis. (B) Quantification of control (black bars) and starvation (white bars) PCR products depicted in A. (C) Average of three different experiments represented as fold differences of starvation compared to control expression. ∗ indicates statistically significant difference between expression in control and starvation for an individual gene ( P
Semi Quantitative Rt Pcr Cdna, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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semi quantitative rt pcr cdna - by Bioz Stars, 2020-07
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1) Product Images from "The role of transcriptional regulation in maintaining the availability of mycobacterial adenylate cyclases"

Article Title: The role of transcriptional regulation in maintaining the availability of mycobacterial adenylate cyclases

Journal: PeerJ

doi: 10.7717/peerj.298

Regulation of M. smegmatis adenylate cyclase genes under starvation conditions. Semi-quantitative RT-PCR was used to compare adenylate cyclase mRNA levels between late-log phase cultures incubated for 4 h in mycomedia (control) or PBS (starvation). (A) A representative depiction of PCR-amplified cDNA separated using agarose gel electrophoresis. (B) Quantification of control (black bars) and starvation (white bars) PCR products depicted in A. (C) Average of three different experiments represented as fold differences of starvation compared to control expression. ∗ indicates statistically significant difference between expression in control and starvation for an individual gene ( P
Figure Legend Snippet: Regulation of M. smegmatis adenylate cyclase genes under starvation conditions. Semi-quantitative RT-PCR was used to compare adenylate cyclase mRNA levels between late-log phase cultures incubated for 4 h in mycomedia (control) or PBS (starvation). (A) A representative depiction of PCR-amplified cDNA separated using agarose gel electrophoresis. (B) Quantification of control (black bars) and starvation (white bars) PCR products depicted in A. (C) Average of three different experiments represented as fold differences of starvation compared to control expression. ∗ indicates statistically significant difference between expression in control and starvation for an individual gene ( P

Techniques Used: Quantitative RT-PCR, Incubation, Polymerase Chain Reaction, Amplification, Agarose Gel Electrophoresis, Expressing

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Reverse Transcription Polymerase Chain Reaction:

Article Title: The role of transcriptional regulation in maintaining the availability of mycobacterial adenylate cyclases
Article Snippet: .. Semi-quantitative RT-PCR cDNA was prepared from 0.5 µg of RNA using the iScript cDNA synthesis kit according to the manufacture’s specifications (BioRad). ..

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    Bio-Rad semi quantitative rt pcr cdna
    Regulation of M. smegmatis adenylate cyclase genes under starvation conditions. Semi-quantitative <t>RT-PCR</t> was used to compare adenylate cyclase mRNA levels between late-log phase cultures incubated for 4 h in mycomedia (control) or PBS (starvation). (A) A representative depiction of PCR-amplified <t>cDNA</t> separated using agarose gel electrophoresis. (B) Quantification of control (black bars) and starvation (white bars) PCR products depicted in A. (C) Average of three different experiments represented as fold differences of starvation compared to control expression. ∗ indicates statistically significant difference between expression in control and starvation for an individual gene ( P
    Semi Quantitative Rt Pcr Cdna, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 88/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/semi quantitative rt pcr cdna/product/Bio-Rad
    Average 88 stars, based on 1 article reviews
    Price from $9.99 to $1999.99
    semi quantitative rt pcr cdna - by Bioz Stars, 2020-07
    88/100 stars
      Buy from Supplier

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    Regulation of M. smegmatis adenylate cyclase genes under starvation conditions. Semi-quantitative RT-PCR was used to compare adenylate cyclase mRNA levels between late-log phase cultures incubated for 4 h in mycomedia (control) or PBS (starvation). (A) A representative depiction of PCR-amplified cDNA separated using agarose gel electrophoresis. (B) Quantification of control (black bars) and starvation (white bars) PCR products depicted in A. (C) Average of three different experiments represented as fold differences of starvation compared to control expression. ∗ indicates statistically significant difference between expression in control and starvation for an individual gene ( P

    Journal: PeerJ

    Article Title: The role of transcriptional regulation in maintaining the availability of mycobacterial adenylate cyclases

    doi: 10.7717/peerj.298

    Figure Lengend Snippet: Regulation of M. smegmatis adenylate cyclase genes under starvation conditions. Semi-quantitative RT-PCR was used to compare adenylate cyclase mRNA levels between late-log phase cultures incubated for 4 h in mycomedia (control) or PBS (starvation). (A) A representative depiction of PCR-amplified cDNA separated using agarose gel electrophoresis. (B) Quantification of control (black bars) and starvation (white bars) PCR products depicted in A. (C) Average of three different experiments represented as fold differences of starvation compared to control expression. ∗ indicates statistically significant difference between expression in control and starvation for an individual gene ( P

    Article Snippet: Semi-quantitative RT-PCR cDNA was prepared from 0.5 µg of RNA using the iScript cDNA synthesis kit according to the manufacture’s specifications (BioRad).

    Techniques: Quantitative RT-PCR, Incubation, Polymerase Chain Reaction, Amplification, Agarose Gel Electrophoresis, Expressing