custom designed deltagene assay primer pairs
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custom designed deltagene assay primer pairs
Figure 4 Single cell qRT-PCR was carried out on a BioMark HD System (Fluidigm) using a 96 × 96 chip.
DELTAgene Assay custom designed primers (Fluidigm) were used for amplification. Technical replicates were generated for each single cell. (A) Histograms showing the distribution of expression of 4 genes in each population. Data shown unnormalized. (B) Single cells were sorted by flow cytometry into LIF withdrawal conditions. After 7 days differentiated colonies were immunostained for GATA6, CDX2 and BRACHYURY. Quantification of marker expression patterns. 2 and 3 marker exclusive expression indicates colonies that contain independent cells positive for different lineage markers. (C) Whole-mount immunostaining of an E6.5 chimeric embryo generated by injection of a single HV+ ES cell constitutively expressed H2B-Tomato, previously cultured in 2i/LIF, into a morula stage wild-type embryo. Upper whole-mount image shows an extended focus view of the entire embryo. Panels below show optical sections, generated by confocal microscopy, with ES cells contributing to trophoblast and visceral and parietal endoderm (VE and PE, respectively). (D) E6.5 chimeras generated by injection of a single HV- cell that had been cultured in 2i/LIF. The majority of single cells contributed only to epiblast (11/13), with only 2 showing extraembryonic contribution. " width="250" height="auto" />
Custom Designed Deltagene Assay Primer Pairs, supplied by fluidigm, used in various techniques. Bioz Stars score: 93/100, based on 32 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and morehttps://www.bioz.com/product/custom+designed+deltagene+assay+primer+pairs/pmc03701323-74-11-17?v=fluidigm
Average 93 stars, based on 32 article reviews
custom designed deltagene assay primer pairs - by
Bioz Stars,
2026-07
93/100 stars
Images
1) Product Images from "Totipotent Embryonic Stem Cells Arise in Ground-State Culture Conditions"
Article Title: Totipotent Embryonic Stem Cells Arise in Ground-State Culture Conditions
Journal: Cell Reports
doi: 10.1016/j.celrep.2013.04.034

Figure 4 Single cell qRT-PCR was carried out on a BioMark HD System (Fluidigm) using a 96 × 96 chip. DELTAgene Assay custom designed primers (Fluidigm) were used for amplification. Technical replicates were generated for each single cell. (A) Histograms showing the distribution of expression of 4 genes in each population. Data shown unnormalized. (B) Single cells were sorted by flow cytometry into LIF withdrawal conditions. After 7 days differentiated colonies were immunostained for GATA6, CDX2 and BRACHYURY. Quantification of marker expression patterns. 2 and 3 marker exclusive expression indicates colonies that contain independent cells positive for different lineage markers. (C) Whole-mount immunostaining of an E6.5 chimeric embryo generated by injection of a single HV+ ES cell constitutively expressed H2B-Tomato, previously cultured in 2i/LIF, into a morula stage wild-type embryo. Upper whole-mount image shows an extended focus view of the entire embryo. Panels below show optical sections, generated by confocal microscopy, with ES cells contributing to trophoblast and visceral and parietal endoderm (VE and PE, respectively). (D) E6.5 chimeras generated by injection of a single HV- cell that had been cultured in 2i/LIF. The majority of single cells contributed only to epiblast (11/13), with only 2 showing extraembryonic contribution. " title="... System (Fluidigm) using a 96 × 96 chip. DELTAgene Assay custom designed primers (Fluidigm) were used for ..." property="contentUrl" width="100%" height="100%"/>
Figure Legend Snippet: Single HV + Cells Are Totipotent in the Ground State, Related to Figure 4 Single cell qRT-PCR was carried out on a BioMark HD System (Fluidigm) using a 96 × 96 chip. DELTAgene Assay custom designed primers (Fluidigm) were used for amplification. Technical replicates were generated for each single cell. (A) Histograms showing the distribution of expression of 4 genes in each population. Data shown unnormalized. (B) Single cells were sorted by flow cytometry into LIF withdrawal conditions. After 7 days differentiated colonies were immunostained for GATA6, CDX2 and BRACHYURY. Quantification of marker expression patterns. 2 and 3 marker exclusive expression indicates colonies that contain independent cells positive for different lineage markers. (C) Whole-mount immunostaining of an E6.5 chimeric embryo generated by injection of a single HV+ ES cell constitutively expressed H2B-Tomato, previously cultured in 2i/LIF, into a morula stage wild-type embryo. Upper whole-mount image shows an extended focus view of the entire embryo. Panels below show optical sections, generated by confocal microscopy, with ES cells contributing to trophoblast and visceral and parietal endoderm (VE and PE, respectively). (D) E6.5 chimeras generated by injection of a single HV- cell that had been cultured in 2i/LIF. The majority of single cells contributed only to epiblast (11/13), with only 2 showing extraembryonic contribution.
Techniques Used: Quantitative RT-PCR, Amplification, Generated, Expressing, Flow Cytometry, Marker, Immunostaining, Injection, Cell Culture, Confocal Microscopy