intact cells Search Results


intact cem cells  (CEM Corporation)
90
CEM Corporation intact cem cells
Intact Cem Cells, supplied by CEM Corporation, 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/intact+cells/intact+cem+cells/us08110577-133-3-2
Average 90 stars, based on 1 article reviews
intact cem cells - by Bioz Stars, 2026-10
90/100 stars
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bl21(de3) cells  (Intact Genomics)
90
Intact Genomics bl21(de3) cells
Bl21(de3) Cells, supplied by Intact Genomics, 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/intact+cells/bl21+de3++cells/pm27708258-273-5-7
Average 90 stars, based on 1 article reviews
bl21(de3) cells - by Bioz Stars, 2026-10
90/100 stars
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e. coli competent cells  (Intact Genomics)
90
Intact Genomics e. coli competent cells
E. Coli Competent Cells, supplied by Intact Genomics, 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/intact+cells/e++coli+competent+cells/pmc05577364-339-40-12
Average 90 stars, based on 1 article reviews
e. coli competent cells - by Bioz Stars, 2026-10
90/100 stars
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intact islet cell architecture  (StemCells Inc)
90
StemCells Inc intact islet cell architecture
Intact Islet Cell Architecture, supplied by StemCells 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/product/intact+cells/intact+islet+cell+architecture/pm22162314-185-5-12
Average 90 stars, based on 1 article reviews
intact islet cell architecture - by Bioz Stars, 2026-10
90/100 stars
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centrifugation of intact cells  (BioNano Genomics)
90
BioNano Genomics centrifugation of intact cells
Centrifugation Of Intact Cells, supplied by BioNano Genomics, 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/intact+cells/centrifugation+of+intact+cells/pm38164980-179-26-27
Average 90 stars, based on 1 article reviews
centrifugation of intact cells - by Bioz Stars, 2026-10
90/100 stars
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viral lysis buffer fastamp viral and cell solution  (Intact Genomics)
90
Intact Genomics viral lysis buffer fastamp viral and cell solution
Viral Lysis Buffer Fastamp Viral And Cell Solution, supplied by Intact Genomics, 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/intact+cells/fastamp+viral+and+cell+solution+for+covid+19+testing/pmc07679446-232-2-10
Average 90 stars, based on 1 article reviews
viral lysis buffer fastamp viral and cell solution - by Bioz Stars, 2026-10
90/100 stars
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electrically competent e. coli cells gt115 strain  (Intact Genomics)
90
Intact Genomics electrically competent e. coli cells gt115 strain
( A ) Y-axis depicts the number of unique plasmid-derived mRNA fragments reported in a given STARR-seq ( ; ; ), MPRA ( ; ; ), or CAP-STARR ( ; ) experiment. Each dot represents a replicate transfection (in cases where data on individual replicates were available). Published STARR-seq, MPRA, or CAP-STARR experiments that did not report the number of unique plasmid-derived mRNA fragments per replicate are not included. ( B ) Retransforming a given plasmid pool results in almost no loss in diversity. We retransformed a small amount (<300 ng) of the plasmid pool described in the main text into 300 ul of electrocompetent <t>GT115</t> E. coli , and sequenced the inserts from the retransformed sample. For a given number of sampled fragments (x-axis), the retransformed sample and the post-transfection DNA-seq plasmid libraries from the main experiment have a comparable number of unique fragments (defined as uniquely mapped fragments with unique start and end positions). Each solid line represents an individual replicate, and the dashed line shows the line where x = y. The retransformed plasmid DNA library appears slightly more diverse than the methylated and unmethylated condition libraries, presumably because ( i ) the methylated and unmethylated condition libraries were sequenced post-transfection (which likely results in some loss of diversity) and (ii) the retransformed plasmid was supercoiled DNA rather than ligation product, likely resulting in a more efficient transfection. Importantly, almost all (98.17%) of fragments observed in the retransformed library are also present in methylated and unmethylated condition libraries.
Electrically Competent E. Coli Cells Gt115 Strain, supplied by Intact Genomics, 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/intact+cells/gt115+strain+electrically+competent+e++coli+cells/pmc06303109-15-6-9
Average 90 stars, based on 1 article reviews
electrically competent e. coli cells gt115 strain - by Bioz Stars, 2026-10
90/100 stars
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intact cells  (The Company of Biologists)
90
The Company of Biologists intact cells
( A ) Y-axis depicts the number of unique plasmid-derived mRNA fragments reported in a given STARR-seq ( ; ; ), MPRA ( ; ; ), or CAP-STARR ( ; ) experiment. Each dot represents a replicate transfection (in cases where data on individual replicates were available). Published STARR-seq, MPRA, or CAP-STARR experiments that did not report the number of unique plasmid-derived mRNA fragments per replicate are not included. ( B ) Retransforming a given plasmid pool results in almost no loss in diversity. We retransformed a small amount (<300 ng) of the plasmid pool described in the main text into 300 ul of electrocompetent <t>GT115</t> E. coli , and sequenced the inserts from the retransformed sample. For a given number of sampled fragments (x-axis), the retransformed sample and the post-transfection DNA-seq plasmid libraries from the main experiment have a comparable number of unique fragments (defined as uniquely mapped fragments with unique start and end positions). Each solid line represents an individual replicate, and the dashed line shows the line where x = y. The retransformed plasmid DNA library appears slightly more diverse than the methylated and unmethylated condition libraries, presumably because ( i ) the methylated and unmethylated condition libraries were sequenced post-transfection (which likely results in some loss of diversity) and (ii) the retransformed plasmid was supercoiled DNA rather than ligation product, likely resulting in a more efficient transfection. Importantly, almost all (98.17%) of fragments observed in the retransformed library are also present in methylated and unmethylated condition libraries.
Intact Cells, supplied by The Company of Biologists, 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/intact+cells/intact+cells/pm10194413-17-21-39
Average 90 stars, based on 1 article reviews
intact cells - by Bioz Stars, 2026-10
90/100 stars
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intact e. coli cells  (Autodisplay Biotech GmbH)
90
Autodisplay Biotech GmbH intact e. coli cells
( A ) Y-axis depicts the number of unique plasmid-derived mRNA fragments reported in a given STARR-seq ( ; ; ), MPRA ( ; ; ), or CAP-STARR ( ; ) experiment. Each dot represents a replicate transfection (in cases where data on individual replicates were available). Published STARR-seq, MPRA, or CAP-STARR experiments that did not report the number of unique plasmid-derived mRNA fragments per replicate are not included. ( B ) Retransforming a given plasmid pool results in almost no loss in diversity. We retransformed a small amount (<300 ng) of the plasmid pool described in the main text into 300 ul of electrocompetent <t>GT115</t> E. coli , and sequenced the inserts from the retransformed sample. For a given number of sampled fragments (x-axis), the retransformed sample and the post-transfection DNA-seq plasmid libraries from the main experiment have a comparable number of unique fragments (defined as uniquely mapped fragments with unique start and end positions). Each solid line represents an individual replicate, and the dashed line shows the line where x = y. The retransformed plasmid DNA library appears slightly more diverse than the methylated and unmethylated condition libraries, presumably because ( i ) the methylated and unmethylated condition libraries were sequenced post-transfection (which likely results in some loss of diversity) and (ii) the retransformed plasmid was supercoiled DNA rather than ligation product, likely resulting in a more efficient transfection. Importantly, almost all (98.17%) of fragments observed in the retransformed library are also present in methylated and unmethylated condition libraries.
Intact E. Coli Cells, supplied by Autodisplay Biotech GmbH, 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/intact+cells/intact+e++coli+cells/pm36692311-126-5-11
Average 90 stars, based on 1 article reviews
intact e. coli cells - by Bioz Stars, 2026-10
90/100 stars
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electro-competent tg1 cells  (Intact Genomics)
90
Intact Genomics electro-competent tg1 cells
( A ) Y-axis depicts the number of unique plasmid-derived mRNA fragments reported in a given STARR-seq ( ; ; ), MPRA ( ; ; ), or CAP-STARR ( ; ) experiment. Each dot represents a replicate transfection (in cases where data on individual replicates were available). Published STARR-seq, MPRA, or CAP-STARR experiments that did not report the number of unique plasmid-derived mRNA fragments per replicate are not included. ( B ) Retransforming a given plasmid pool results in almost no loss in diversity. We retransformed a small amount (<300 ng) of the plasmid pool described in the main text into 300 ul of electrocompetent <t>GT115</t> E. coli , and sequenced the inserts from the retransformed sample. For a given number of sampled fragments (x-axis), the retransformed sample and the post-transfection DNA-seq plasmid libraries from the main experiment have a comparable number of unique fragments (defined as uniquely mapped fragments with unique start and end positions). Each solid line represents an individual replicate, and the dashed line shows the line where x = y. The retransformed plasmid DNA library appears slightly more diverse than the methylated and unmethylated condition libraries, presumably because ( i ) the methylated and unmethylated condition libraries were sequenced post-transfection (which likely results in some loss of diversity) and (ii) the retransformed plasmid was supercoiled DNA rather than ligation product, likely resulting in a more efficient transfection. Importantly, almost all (98.17%) of fragments observed in the retransformed library are also present in methylated and unmethylated condition libraries.
Electro Competent Tg1 Cells, supplied by Intact Genomics, 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/intact+cells/electro+competent+tg1+cells/pmc11107207-257-108-110
Average 90 stars, based on 1 article reviews
electro-competent tg1 cells - by Bioz Stars, 2026-10
90/100 stars
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intact mouse cardiac muscle cells  (Japan SLC inc)
90
Japan SLC inc intact mouse cardiac muscle cells
( A ) Y-axis depicts the number of unique plasmid-derived mRNA fragments reported in a given STARR-seq ( ; ; ), MPRA ( ; ; ), or CAP-STARR ( ; ) experiment. Each dot represents a replicate transfection (in cases where data on individual replicates were available). Published STARR-seq, MPRA, or CAP-STARR experiments that did not report the number of unique plasmid-derived mRNA fragments per replicate are not included. ( B ) Retransforming a given plasmid pool results in almost no loss in diversity. We retransformed a small amount (<300 ng) of the plasmid pool described in the main text into 300 ul of electrocompetent <t>GT115</t> E. coli , and sequenced the inserts from the retransformed sample. For a given number of sampled fragments (x-axis), the retransformed sample and the post-transfection DNA-seq plasmid libraries from the main experiment have a comparable number of unique fragments (defined as uniquely mapped fragments with unique start and end positions). Each solid line represents an individual replicate, and the dashed line shows the line where x = y. The retransformed plasmid DNA library appears slightly more diverse than the methylated and unmethylated condition libraries, presumably because ( i ) the methylated and unmethylated condition libraries were sequenced post-transfection (which likely results in some loss of diversity) and (ii) the retransformed plasmid was supercoiled DNA rather than ligation product, likely resulting in a more efficient transfection. Importantly, almost all (98.17%) of fragments observed in the retransformed library are also present in methylated and unmethylated condition libraries.
Intact Mouse Cardiac Muscle Cells, supplied by Japan SLC 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/product/intact+cells/intact+mouse+cardiac+muscle+cells/us11920180-158-40-70
Average 90 stars, based on 1 article reviews
intact mouse cardiac muscle cells - by Bioz Stars, 2026-10
90/100 stars
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intact human t-leukemia cells (ccrf-cem cells)  (CEM Corporation)
90
CEM Corporation intact human t-leukemia cells (ccrf-cem cells)
( A ) Y-axis depicts the number of unique plasmid-derived mRNA fragments reported in a given STARR-seq ( ; ; ), MPRA ( ; ; ), or CAP-STARR ( ; ) experiment. Each dot represents a replicate transfection (in cases where data on individual replicates were available). Published STARR-seq, MPRA, or CAP-STARR experiments that did not report the number of unique plasmid-derived mRNA fragments per replicate are not included. ( B ) Retransforming a given plasmid pool results in almost no loss in diversity. We retransformed a small amount (<300 ng) of the plasmid pool described in the main text into 300 ul of electrocompetent <t>GT115</t> E. coli , and sequenced the inserts from the retransformed sample. For a given number of sampled fragments (x-axis), the retransformed sample and the post-transfection DNA-seq plasmid libraries from the main experiment have a comparable number of unique fragments (defined as uniquely mapped fragments with unique start and end positions). Each solid line represents an individual replicate, and the dashed line shows the line where x = y. The retransformed plasmid DNA library appears slightly more diverse than the methylated and unmethylated condition libraries, presumably because ( i ) the methylated and unmethylated condition libraries were sequenced post-transfection (which likely results in some loss of diversity) and (ii) the retransformed plasmid was supercoiled DNA rather than ligation product, likely resulting in a more efficient transfection. Importantly, almost all (98.17%) of fragments observed in the retransformed library are also present in methylated and unmethylated condition libraries.
Intact Human T Leukemia Cells (Ccrf Cem Cells), supplied by CEM Corporation, 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/intact+cells/intact+human+t+leukemia+cells++ccrf+cem+cells+/pm33945753-121-28-31
Average 90 stars, based on 1 article reviews
intact human t-leukemia cells (ccrf-cem cells) - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


( A ) Y-axis depicts the number of unique plasmid-derived mRNA fragments reported in a given STARR-seq ( ; ; ), MPRA ( ; ; ), or CAP-STARR ( ; ) experiment. Each dot represents a replicate transfection (in cases where data on individual replicates were available). Published STARR-seq, MPRA, or CAP-STARR experiments that did not report the number of unique plasmid-derived mRNA fragments per replicate are not included. ( B ) Retransforming a given plasmid pool results in almost no loss in diversity. We retransformed a small amount (<300 ng) of the plasmid pool described in the main text into 300 ul of electrocompetent GT115 E. coli , and sequenced the inserts from the retransformed sample. For a given number of sampled fragments (x-axis), the retransformed sample and the post-transfection DNA-seq plasmid libraries from the main experiment have a comparable number of unique fragments (defined as uniquely mapped fragments with unique start and end positions). Each solid line represents an individual replicate, and the dashed line shows the line where x = y. The retransformed plasmid DNA library appears slightly more diverse than the methylated and unmethylated condition libraries, presumably because ( i ) the methylated and unmethylated condition libraries were sequenced post-transfection (which likely results in some loss of diversity) and (ii) the retransformed plasmid was supercoiled DNA rather than ligation product, likely resulting in a more efficient transfection. Importantly, almost all (98.17%) of fragments observed in the retransformed library are also present in methylated and unmethylated condition libraries.

Journal: eLife

Article Title: Genome-wide quantification of the effects of DNA methylation on human gene regulation

doi: 10.7554/eLife.37513

Figure Lengend Snippet: ( A ) Y-axis depicts the number of unique plasmid-derived mRNA fragments reported in a given STARR-seq ( ; ; ), MPRA ( ; ; ), or CAP-STARR ( ; ) experiment. Each dot represents a replicate transfection (in cases where data on individual replicates were available). Published STARR-seq, MPRA, or CAP-STARR experiments that did not report the number of unique plasmid-derived mRNA fragments per replicate are not included. ( B ) Retransforming a given plasmid pool results in almost no loss in diversity. We retransformed a small amount (<300 ng) of the plasmid pool described in the main text into 300 ul of electrocompetent GT115 E. coli , and sequenced the inserts from the retransformed sample. For a given number of sampled fragments (x-axis), the retransformed sample and the post-transfection DNA-seq plasmid libraries from the main experiment have a comparable number of unique fragments (defined as uniquely mapped fragments with unique start and end positions). Each solid line represents an individual replicate, and the dashed line shows the line where x = y. The retransformed plasmid DNA library appears slightly more diverse than the methylated and unmethylated condition libraries, presumably because ( i ) the methylated and unmethylated condition libraries were sequenced post-transfection (which likely results in some loss of diversity) and (ii) the retransformed plasmid was supercoiled DNA rather than ligation product, likely resulting in a more efficient transfection. Importantly, almost all (98.17%) of fragments observed in the retransformed library are also present in methylated and unmethylated condition libraries.

Article Snippet: Electrically competent E. coli cells , GT115 strain , Intact Genomics , , Custom order to grow Invivogen's ChemiComp GT115 strain and prepare cells for electroporation.

Techniques: Plasmid Preparation, Derivative Assay, Transfection, DNA Sequencing, Methylation, Ligation

Journal: eLife

Article Title: Genome-wide quantification of the effects of DNA methylation on human gene regulation

doi: 10.7554/eLife.37513

Figure Lengend Snippet:

Article Snippet: Electrically competent E. coli cells , GT115 strain , Intact Genomics , , Custom order to grow Invivogen's ChemiComp GT115 strain and prepare cells for electroporation.

Techniques: Recombinant, Plasmid Preparation, Electroporation