Review





Similar Products

86
Amaxa amaxa basic nucleofector kit
Amaxa Basic Nucleofector Kit, supplied by Amaxa, 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/amaxa+nucleofector+kit/pmc13266002-306-14-14?v=Amaxa
Average 86 stars, based on 1 article reviews
amaxa basic nucleofector kit - by Bioz Stars, 2026-07
86/100 stars
  Buy from Supplier

86
Amaxa 2b amaxa human cd34 cell nucleofector kit
a Schematic representation of human α-globin locus on chromosome 16p13.3. From the telomeric end, the locus contains the ζ-globin gene HBZ , the minor μ-globin gene HBM , the two α-globin genes HBA2 and HBA1 , and lastly the minor θ-globin gene HBQ1 . Two pseudogenes are present: ψζ HBZP1 between HBZ and HBM , and ψα1 HBAP1 between HBM and HBA2 . Four distal enhancers (R1-R4) are situated upstream of the genes. b Schematic overview of the experimental workflow to generate ATRX knockout erythroid cells from healthy donor <t>CD34</t> + HSPCs, followed by downstream analysis. c Western blot analysis of ATRX expression in day 7 differentiated cells, confirming efficient knockout. Quantification is presented on the right (n = 3 biological replicates, data shown as mean ± SEM). ** p = 0.009, two-tailed unpaired Welch’s t-test. d Relative expression of HBA, HBM and α to β-like globin ratios by RT-qPCR analysis in day 10 and day 13 differentiated erythroid cells (n = 3 biological replicates, data shown as mean ± SEM). Differences between AAVS1 and ATRX KO were compared using a two-tailed unpaired Welch’s t-test on log₂-transformed fold-change values. e Genotyping summary of the collected 351 BFU-E colonies derived from ATRX KO samples showing genotype distribution. f Three-dimensional plot showing Biomark gene expression analysis of ATRX, HBA and HBM in single BFU-E colony. Each dot represents one colony, and the edited AAVS1 colonies are shown in blue; ATRX KO colonies with frameshift mutations (ATRX_FS) are shown in red. AAVS1 controls gather around the internal space whereas the majority of the ATRX KO colonies assemble around the origin indicating low expression of ATRX, HBM and HBA . g Quantified gene expression analyses of BFU-E colonies show statistical differences between AAVS1 (n = 15) and ATRX KO groups (n = 57) (Mann-Whitney U test). Individual colonies are selected from two biological repeats. *** p = 1.493 × 10 -5 for ATRX expression, ** p = 0.003632 for HBM expression, and p = 0.9083 for HBA expression. ns: not significant. Source data are provided as a Source Data file.
2b Amaxa Human Cd34 Cell Nucleofector Kit, supplied by Amaxa, 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/amaxa+nucleofector+kit/pmc13018553-336-18-19?v=Amaxa
Average 86 stars, based on 1 article reviews
2b amaxa human cd34 cell nucleofector kit - by Bioz Stars, 2026-07
86/100 stars
  Buy from Supplier

86
Amaxa 633 amaxa cell line nucleofector kit v
a Schematic representation of human α-globin locus on chromosome 16p13.3. From the telomeric end, the locus contains the ζ-globin gene HBZ , the minor μ-globin gene HBM , the two α-globin genes HBA2 and HBA1 , and lastly the minor θ-globin gene HBQ1 . Two pseudogenes are present: ψζ HBZP1 between HBZ and HBM , and ψα1 HBAP1 between HBM and HBA2 . Four distal enhancers (R1-R4) are situated upstream of the genes. b Schematic overview of the experimental workflow to generate ATRX knockout erythroid cells from healthy donor <t>CD34</t> + HSPCs, followed by downstream analysis. c Western blot analysis of ATRX expression in day 7 differentiated cells, confirming efficient knockout. Quantification is presented on the right (n = 3 biological replicates, data shown as mean ± SEM). ** p = 0.009, two-tailed unpaired Welch’s t-test. d Relative expression of HBA, HBM and α to β-like globin ratios by RT-qPCR analysis in day 10 and day 13 differentiated erythroid cells (n = 3 biological replicates, data shown as mean ± SEM). Differences between AAVS1 and ATRX KO were compared using a two-tailed unpaired Welch’s t-test on log₂-transformed fold-change values. e Genotyping summary of the collected 351 BFU-E colonies derived from ATRX KO samples showing genotype distribution. f Three-dimensional plot showing Biomark gene expression analysis of ATRX, HBA and HBM in single BFU-E colony. Each dot represents one colony, and the edited AAVS1 colonies are shown in blue; ATRX KO colonies with frameshift mutations (ATRX_FS) are shown in red. AAVS1 controls gather around the internal space whereas the majority of the ATRX KO colonies assemble around the origin indicating low expression of ATRX, HBM and HBA . g Quantified gene expression analyses of BFU-E colonies show statistical differences between AAVS1 (n = 15) and ATRX KO groups (n = 57) (Mann-Whitney U test). Individual colonies are selected from two biological repeats. *** p = 1.493 × 10 -5 for ATRX expression, ** p = 0.003632 for HBM expression, and p = 0.9083 for HBA expression. ns: not significant. Source data are provided as a Source Data file.
633 Amaxa Cell Line Nucleofector Kit V, supplied by Amaxa, 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/amaxa+nucleofector+kit/pm41376157-278-14-15?v=Amaxa
Average 86 stars, based on 1 article reviews
633 amaxa cell line nucleofector kit v - by Bioz Stars, 2026-07
86/100 stars
  Buy from Supplier

86
Amaxa amaxa nucleofector kit t
a Schematic representation of human α-globin locus on chromosome 16p13.3. From the telomeric end, the locus contains the ζ-globin gene HBZ , the minor μ-globin gene HBM , the two α-globin genes HBA2 and HBA1 , and lastly the minor θ-globin gene HBQ1 . Two pseudogenes are present: ψζ HBZP1 between HBZ and HBM , and ψα1 HBAP1 between HBM and HBA2 . Four distal enhancers (R1-R4) are situated upstream of the genes. b Schematic overview of the experimental workflow to generate ATRX knockout erythroid cells from healthy donor <t>CD34</t> + HSPCs, followed by downstream analysis. c Western blot analysis of ATRX expression in day 7 differentiated cells, confirming efficient knockout. Quantification is presented on the right (n = 3 biological replicates, data shown as mean ± SEM). ** p = 0.009, two-tailed unpaired Welch’s t-test. d Relative expression of HBA, HBM and α to β-like globin ratios by RT-qPCR analysis in day 10 and day 13 differentiated erythroid cells (n = 3 biological replicates, data shown as mean ± SEM). Differences between AAVS1 and ATRX KO were compared using a two-tailed unpaired Welch’s t-test on log₂-transformed fold-change values. e Genotyping summary of the collected 351 BFU-E colonies derived from ATRX KO samples showing genotype distribution. f Three-dimensional plot showing Biomark gene expression analysis of ATRX, HBA and HBM in single BFU-E colony. Each dot represents one colony, and the edited AAVS1 colonies are shown in blue; ATRX KO colonies with frameshift mutations (ATRX_FS) are shown in red. AAVS1 controls gather around the internal space whereas the majority of the ATRX KO colonies assemble around the origin indicating low expression of ATRX, HBM and HBA . g Quantified gene expression analyses of BFU-E colonies show statistical differences between AAVS1 (n = 15) and ATRX KO groups (n = 57) (Mann-Whitney U test). Individual colonies are selected from two biological repeats. *** p = 1.493 × 10 -5 for ATRX expression, ** p = 0.003632 for HBM expression, and p = 0.9083 for HBA expression. ns: not significant. Source data are provided as a Source Data file.
Amaxa Nucleofector Kit T, supplied by Amaxa, 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/amaxa+nucleofector+kit/us12478672-188-12-12?v=Amaxa
Average 86 stars, based on 1 article reviews
amaxa nucleofector kit t - by Bioz Stars, 2026-07
86/100 stars
  Buy from Supplier

90
Amaxa amaxa® cell line nucleofector® kit v
a Schematic representation of human α-globin locus on chromosome 16p13.3. From the telomeric end, the locus contains the ζ-globin gene HBZ , the minor μ-globin gene HBM , the two α-globin genes HBA2 and HBA1 , and lastly the minor θ-globin gene HBQ1 . Two pseudogenes are present: ψζ HBZP1 between HBZ and HBM , and ψα1 HBAP1 between HBM and HBA2 . Four distal enhancers (R1-R4) are situated upstream of the genes. b Schematic overview of the experimental workflow to generate ATRX knockout erythroid cells from healthy donor <t>CD34</t> + HSPCs, followed by downstream analysis. c Western blot analysis of ATRX expression in day 7 differentiated cells, confirming efficient knockout. Quantification is presented on the right (n = 3 biological replicates, data shown as mean ± SEM). ** p = 0.009, two-tailed unpaired Welch’s t-test. d Relative expression of HBA, HBM and α to β-like globin ratios by RT-qPCR analysis in day 10 and day 13 differentiated erythroid cells (n = 3 biological replicates, data shown as mean ± SEM). Differences between AAVS1 and ATRX KO were compared using a two-tailed unpaired Welch’s t-test on log₂-transformed fold-change values. e Genotyping summary of the collected 351 BFU-E colonies derived from ATRX KO samples showing genotype distribution. f Three-dimensional plot showing Biomark gene expression analysis of ATRX, HBA and HBM in single BFU-E colony. Each dot represents one colony, and the edited AAVS1 colonies are shown in blue; ATRX KO colonies with frameshift mutations (ATRX_FS) are shown in red. AAVS1 controls gather around the internal space whereas the majority of the ATRX KO colonies assemble around the origin indicating low expression of ATRX, HBM and HBA . g Quantified gene expression analyses of BFU-E colonies show statistical differences between AAVS1 (n = 15) and ATRX KO groups (n = 57) (Mann-Whitney U test). Individual colonies are selected from two biological repeats. *** p = 1.493 × 10 -5 for ATRX expression, ** p = 0.003632 for HBM expression, and p = 0.9083 for HBA expression. ns: not significant. Source data are provided as a Source Data file.
Amaxa® Cell Line Nucleofector® Kit V, supplied by Amaxa, 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/amaxa+nucleofector+kit/pmc10756265__pnas__2318274120__sapp-50-30-29?v=Amaxa
Average 90 stars, based on 1 article reviews
amaxa® cell line nucleofector® kit v - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

90
Amaxa amaxa® human cd34+ cell nucleofector® kit
a Schematic representation of human α-globin locus on chromosome 16p13.3. From the telomeric end, the locus contains the ζ-globin gene HBZ , the minor μ-globin gene HBM , the two α-globin genes HBA2 and HBA1 , and lastly the minor θ-globin gene HBQ1 . Two pseudogenes are present: ψζ HBZP1 between HBZ and HBM , and ψα1 HBAP1 between HBM and HBA2 . Four distal enhancers (R1-R4) are situated upstream of the genes. b Schematic overview of the experimental workflow to generate ATRX knockout erythroid cells from healthy donor <t>CD34</t> + HSPCs, followed by downstream analysis. c Western blot analysis of ATRX expression in day 7 differentiated cells, confirming efficient knockout. Quantification is presented on the right (n = 3 biological replicates, data shown as mean ± SEM). ** p = 0.009, two-tailed unpaired Welch’s t-test. d Relative expression of HBA, HBM and α to β-like globin ratios by RT-qPCR analysis in day 10 and day 13 differentiated erythroid cells (n = 3 biological replicates, data shown as mean ± SEM). Differences between AAVS1 and ATRX KO were compared using a two-tailed unpaired Welch’s t-test on log₂-transformed fold-change values. e Genotyping summary of the collected 351 BFU-E colonies derived from ATRX KO samples showing genotype distribution. f Three-dimensional plot showing Biomark gene expression analysis of ATRX, HBA and HBM in single BFU-E colony. Each dot represents one colony, and the edited AAVS1 colonies are shown in blue; ATRX KO colonies with frameshift mutations (ATRX_FS) are shown in red. AAVS1 controls gather around the internal space whereas the majority of the ATRX KO colonies assemble around the origin indicating low expression of ATRX, HBM and HBA . g Quantified gene expression analyses of BFU-E colonies show statistical differences between AAVS1 (n = 15) and ATRX KO groups (n = 57) (Mann-Whitney U test). Individual colonies are selected from two biological repeats. *** p = 1.493 × 10 -5 for ATRX expression, ** p = 0.003632 for HBM expression, and p = 0.9083 for HBA expression. ns: not significant. Source data are provided as a Source Data file.
Amaxa® Human Cd34+ Cell Nucleofector® Kit, supplied by Amaxa, 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/amaxa+nucleofector+kit/pm39970510-27-22-21?v=Amaxa
Average 90 stars, based on 1 article reviews
amaxa® human cd34+ cell nucleofector® kit - by Bioz Stars, 2026-07
90/100 stars
  Buy from Supplier

Image Search Results


a Schematic representation of human α-globin locus on chromosome 16p13.3. From the telomeric end, the locus contains the ζ-globin gene HBZ , the minor μ-globin gene HBM , the two α-globin genes HBA2 and HBA1 , and lastly the minor θ-globin gene HBQ1 . Two pseudogenes are present: ψζ HBZP1 between HBZ and HBM , and ψα1 HBAP1 between HBM and HBA2 . Four distal enhancers (R1-R4) are situated upstream of the genes. b Schematic overview of the experimental workflow to generate ATRX knockout erythroid cells from healthy donor CD34 + HSPCs, followed by downstream analysis. c Western blot analysis of ATRX expression in day 7 differentiated cells, confirming efficient knockout. Quantification is presented on the right (n = 3 biological replicates, data shown as mean ± SEM). ** p = 0.009, two-tailed unpaired Welch’s t-test. d Relative expression of HBA, HBM and α to β-like globin ratios by RT-qPCR analysis in day 10 and day 13 differentiated erythroid cells (n = 3 biological replicates, data shown as mean ± SEM). Differences between AAVS1 and ATRX KO were compared using a two-tailed unpaired Welch’s t-test on log₂-transformed fold-change values. e Genotyping summary of the collected 351 BFU-E colonies derived from ATRX KO samples showing genotype distribution. f Three-dimensional plot showing Biomark gene expression analysis of ATRX, HBA and HBM in single BFU-E colony. Each dot represents one colony, and the edited AAVS1 colonies are shown in blue; ATRX KO colonies with frameshift mutations (ATRX_FS) are shown in red. AAVS1 controls gather around the internal space whereas the majority of the ATRX KO colonies assemble around the origin indicating low expression of ATRX, HBM and HBA . g Quantified gene expression analyses of BFU-E colonies show statistical differences between AAVS1 (n = 15) and ATRX KO groups (n = 57) (Mann-Whitney U test). Individual colonies are selected from two biological repeats. *** p = 1.493 × 10 -5 for ATRX expression, ** p = 0.003632 for HBM expression, and p = 0.9083 for HBA expression. ns: not significant. Source data are provided as a Source Data file.

Journal: Nature Communications

Article Title: ATRX loss couples genome instability at a G-rich repeat to dysregulation of human alpha-globin expression

doi: 10.1038/s41467-026-69169-7

Figure Lengend Snippet: a Schematic representation of human α-globin locus on chromosome 16p13.3. From the telomeric end, the locus contains the ζ-globin gene HBZ , the minor μ-globin gene HBM , the two α-globin genes HBA2 and HBA1 , and lastly the minor θ-globin gene HBQ1 . Two pseudogenes are present: ψζ HBZP1 between HBZ and HBM , and ψα1 HBAP1 between HBM and HBA2 . Four distal enhancers (R1-R4) are situated upstream of the genes. b Schematic overview of the experimental workflow to generate ATRX knockout erythroid cells from healthy donor CD34 + HSPCs, followed by downstream analysis. c Western blot analysis of ATRX expression in day 7 differentiated cells, confirming efficient knockout. Quantification is presented on the right (n = 3 biological replicates, data shown as mean ± SEM). ** p = 0.009, two-tailed unpaired Welch’s t-test. d Relative expression of HBA, HBM and α to β-like globin ratios by RT-qPCR analysis in day 10 and day 13 differentiated erythroid cells (n = 3 biological replicates, data shown as mean ± SEM). Differences between AAVS1 and ATRX KO were compared using a two-tailed unpaired Welch’s t-test on log₂-transformed fold-change values. e Genotyping summary of the collected 351 BFU-E colonies derived from ATRX KO samples showing genotype distribution. f Three-dimensional plot showing Biomark gene expression analysis of ATRX, HBA and HBM in single BFU-E colony. Each dot represents one colony, and the edited AAVS1 colonies are shown in blue; ATRX KO colonies with frameshift mutations (ATRX_FS) are shown in red. AAVS1 controls gather around the internal space whereas the majority of the ATRX KO colonies assemble around the origin indicating low expression of ATRX, HBM and HBA . g Quantified gene expression analyses of BFU-E colonies show statistical differences between AAVS1 (n = 15) and ATRX KO groups (n = 57) (Mann-Whitney U test). Individual colonies are selected from two biological repeats. *** p = 1.493 × 10 -5 for ATRX expression, ** p = 0.003632 for HBM expression, and p = 0.9083 for HBA expression. ns: not significant. Source data are provided as a Source Data file.

Article Snippet: 2 × 10 6 of ATRX degron-VNTR KO differentiated day 6 cells were transfected with RNPs using the 2B Amaxa Human CD34 Cell Nucleofector Kit on the AMAXA Nucleofector 2B system.

Techniques: Knock-Out, Western Blot, Expressing, Two Tailed Test, Quantitative RT-PCR, Transformation Assay, Derivative Assay, Gene Expression, MANN-WHITNEY