rt cdna synthesis kit Search Results


rt ramda cdna synthesis kit  (Toyobo)
96
Toyobo rt ramda cdna synthesis kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Rt Ramda Cdna Synthesis Kit, supplied by Toyobo, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
rt ramda cdna synthesis kit - by Bioz Stars, 2026-02
96/100 stars
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firescript cdna synthesis kit  (Solis BioDyne)
96
Solis BioDyne firescript cdna synthesis kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Firescript Cdna Synthesis Kit, supplied by Solis BioDyne, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 96 stars, based on 1 article reviews
firescript cdna synthesis kit - by Bioz Stars, 2026-02
96/100 stars
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quantaccuracytm rt ramdm cdna synthesis kit  (Toyobo)
93
Toyobo quantaccuracytm rt ramdm cdna synthesis kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Quantaccuracytm Rt Ramdm Cdna Synthesis Kit, supplied by Toyobo, 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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Average 93 stars, based on 1 article reviews
quantaccuracytm rt ramdm cdna synthesis kit - by Bioz Stars, 2026-02
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reverse transcriptase  (Solis BioDyne)
93
Solis BioDyne reverse transcriptase
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Reverse Transcriptase, supplied by Solis BioDyne, 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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Average 93 stars, based on 1 article reviews
reverse transcriptase - by Bioz Stars, 2026-02
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universal rt microrna pcr; polyadenylation cdna synthesis kit  (Qiagen)
90
Qiagen universal rt microrna pcr; polyadenylation cdna synthesis kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Universal Rt Microrna Pcr; Polyadenylation Cdna Synthesis Kit, supplied by Qiagen, 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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Average 90 stars, based on 1 article reviews
universal rt microrna pcr; polyadenylation cdna synthesis kit - by Bioz Stars, 2026-02
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rt first strand cdna synthesis kit  (Servicebio Inc)
90
Servicebio Inc rt first strand cdna synthesis kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Rt First Strand Cdna Synthesis Kit, supplied by Servicebio 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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Average 90 stars, based on 1 article reviews
rt first strand cdna synthesis kit - by Bioz Stars, 2026-02
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rt first strand cdna synthesis kit g3330  (Servicebio Inc)
90
Servicebio Inc rt first strand cdna synthesis kit g3330
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Rt First Strand Cdna Synthesis Kit G3330, supplied by Servicebio 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/rt first strand cdna synthesis kit g3330/product/Servicebio Inc
Average 90 stars, based on 1 article reviews
rt first strand cdna synthesis kit g3330 - by Bioz Stars, 2026-02
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wonder rt cdna synthesis kit  (EuroClone)
90
EuroClone wonder rt cdna synthesis kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Wonder Rt Cdna Synthesis Kit, supplied by EuroClone, 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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Average 90 stars, based on 1 article reviews
wonder rt cdna synthesis kit - by Bioz Stars, 2026-02
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suprimescript cdna synthesis kit  (Genet Bio Inc)
90
Genet Bio Inc suprimescript cdna synthesis kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Suprimescript Cdna Synthesis Kit, supplied by Genet Bio 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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Average 90 stars, based on 1 article reviews
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pcr cdna synthesis kit  (Promega)
90
Promega pcr cdna synthesis kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Pcr Cdna Synthesis 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
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Average 90 stars, based on 1 article reviews
pcr cdna synthesis kit - by Bioz Stars, 2026-02
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cdna first-strand synthesis kit quantscript rt kit  (tiangen biotech co)
90
tiangen biotech co cdna first-strand synthesis kit quantscript rt kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Cdna First Strand Synthesis Kit Quantscript Rt Kit, supplied by tiangen biotech co, 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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swescript rt i first-strand cdna synthesis kit  (Servicebio Inc)
90
Servicebio Inc swescript rt i first-strand cdna synthesis kit
Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific <t>cDNA</t> amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.
Swescript Rt I First Strand Cdna Synthesis Kit, supplied by Servicebio 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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Image Search Results


Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific cDNA amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.

Journal: Stem Cell Reports

Article Title: Early reactivation of clustered genes on the inactive X chromosome during somatic cell reprogramming

doi: 10.1016/j.stemcr.2021.11.008

Figure Lengend Snippet: Establishment of a TaqMan-based system to quantify allele-specific transcripts from the X chromosomes (A) Isolation of hybrid MEFs for XCR analyses. (B) TaqMan probes that discriminate transcripts from B6 and Sp alleles. TaqMan probes in a single reaction recognize their cognate allele-specific transcripts, which differ by SNPs or an MNP, and emit fluorescence (VIC or FAM). (C) Mouse X chromosome showing the locations of Lamp2 , Atrx , and the X-inactivation center (Xic). (D) Linear correlation between the ratio of the allele-specific cDNA amounts and the ratio of emitted fluorescence for each allele. cDNAs derived from homozygous B6 and Sp mice were mixed at five different ratios, and qRT-PCR was performed using TaqMan probes for the Lamp2 or Atrx gene. The square of the correlation coefficient is indicated by R 2 . (E) Relative abundance of allele-specific transcripts in drug-selected MEFs. The relative abundances of allele-specific transcripts in HAT- or 6-TG-selected bsMEFs were calculated by using TaqMan probes for Lamp2 or Atrx . Data represent mean ± SEM of at least three independent experiments. ∗ p < 0.05 and ∗∗ p < 0.01. n.s., not significant.

Article Snippet: Dissociated cells were subjected to single-cell sorting using MoFlo XDP (Beckman) followed by cDNA synthesis using the RT-RamDA cDNA Synthesis Kit (Toyobo).

Techniques: Isolation, Fluorescence, Derivative Assay, Quantitative RT-PCR