pcagig backbone Search Results


97
New England Biolabs pcaggs vector backbone
Pcaggs Vector Backbone, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Addgene inc pcagig backbone
Pcagig Backbone, supplied by Addgene inc, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Addgene inc aflii sali digested pcaggs backbone
Aflii Sali Digested Pcaggs Backbone, supplied by Addgene inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Addgene inc plasmid 92141 backbone
Plasmid 92141 Backbone, supplied by Addgene inc, used in various techniques. Bioz Stars score: 92/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Addgene inc paav backbone
Paav Backbone, supplied by Addgene inc, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Marburg GmbH full-length marburg virus vp40
Full Length Marburg Virus Vp40, supplied by Marburg GmbH, 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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99
New England Biolabs backbone pcaggs vector
Backbone Pcaggs Vector, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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90
Applied Biological Materials Inc ascl1 plasmid
(A) Schematic diagram of NEP. (B) Delivery of Ascl1, Brn2 and <t>Myt1l</t> in MEF cells by NEP. Phenotypic characterization of induced neuron-like cells 2 weeks post-NEP (C) or 4 weeks post-NEP (D). Molecular markers are indicated on the top of each panel. Scale, 50 μM. (E) Ngf expression at weeks 1 and 4 post-NEP. NGF ELISA from differentiated MEF media at 4 weeks post-NEP (n = 10). RT-qPCR analysis of neurotrophin mRNA at (F) 1 week (n = 4) and (G) 4 weeks (n = 6) post-NEP. Data expressed as mean ± SEM, *P < 0.05.
Ascl1 Plasmid, supplied by Applied Biological Materials 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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96
New England Biolabs pcagg mcs wpre backbone
(A) Schematic diagram of NEP. (B) Delivery of Ascl1, Brn2 and <t>Myt1l</t> in MEF cells by NEP. Phenotypic characterization of induced neuron-like cells 2 weeks post-NEP (C) or 4 weeks post-NEP (D). Molecular markers are indicated on the top of each panel. Scale, 50 μM. (E) Ngf expression at weeks 1 and 4 post-NEP. NGF ELISA from differentiated MEF media at 4 weeks post-NEP (n = 10). RT-qPCR analysis of neurotrophin mRNA at (F) 1 week (n = 4) and (G) 4 weeks (n = 6) post-NEP. Data expressed as mean ± SEM, *P < 0.05.
Pcagg Mcs Wpre Backbone, supplied by New England Biolabs, 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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99
New England Biolabs pcagig
(A) Schematic diagram of NEP. (B) Delivery of Ascl1, Brn2 and <t>Myt1l</t> in MEF cells by NEP. Phenotypic characterization of induced neuron-like cells 2 weeks post-NEP (C) or 4 weeks post-NEP (D). Molecular markers are indicated on the top of each panel. Scale, 50 μM. (E) Ngf expression at weeks 1 and 4 post-NEP. NGF ELISA from differentiated MEF media at 4 weeks post-NEP (n = 10). RT-qPCR analysis of neurotrophin mRNA at (F) 1 week (n = 4) and (G) 4 weeks (n = 6) post-NEP. Data expressed as mean ± SEM, *P < 0.05.
Pcagig, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/pcagig/product/New England Biolabs
Average 99 stars, based on 1 article reviews
pcagig - by Bioz Stars, 2026-04
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93
Addgene inc pcaggs backbone
(A) Schematic diagram of NEP. (B) Delivery of Ascl1, Brn2 and <t>Myt1l</t> in MEF cells by NEP. Phenotypic characterization of induced neuron-like cells 2 weeks post-NEP (C) or 4 weeks post-NEP (D). Molecular markers are indicated on the top of each panel. Scale, 50 μM. (E) Ngf expression at weeks 1 and 4 post-NEP. NGF ELISA from differentiated MEF media at 4 weeks post-NEP (n = 10). RT-qPCR analysis of neurotrophin mRNA at (F) 1 week (n = 4) and (G) 4 weeks (n = 6) post-NEP. Data expressed as mean ± SEM, *P < 0.05.
Pcaggs Backbone, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/pcaggs backbone/product/Addgene inc
Average 93 stars, based on 1 article reviews
pcaggs backbone - by Bioz Stars, 2026-04
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Image Search Results


(A) Schematic diagram of NEP. (B) Delivery of Ascl1, Brn2 and Myt1l in MEF cells by NEP. Phenotypic characterization of induced neuron-like cells 2 weeks post-NEP (C) or 4 weeks post-NEP (D). Molecular markers are indicated on the top of each panel. Scale, 50 μM. (E) Ngf expression at weeks 1 and 4 post-NEP. NGF ELISA from differentiated MEF media at 4 weeks post-NEP (n = 10). RT-qPCR analysis of neurotrophin mRNA at (F) 1 week (n = 4) and (G) 4 weeks (n = 6) post-NEP. Data expressed as mean ± SEM, *P < 0.05.

Journal: Nanomedicine : nanotechnology, biology, and medicine

Article Title: Neurogenic tissue nanotransfection in the management of cutaneous diabetic polyneuropathy

doi: 10.1016/j.nano.2020.102220

Figure Lengend Snippet: (A) Schematic diagram of NEP. (B) Delivery of Ascl1, Brn2 and Myt1l in MEF cells by NEP. Phenotypic characterization of induced neuron-like cells 2 weeks post-NEP (C) or 4 weeks post-NEP (D). Molecular markers are indicated on the top of each panel. Scale, 50 μM. (E) Ngf expression at weeks 1 and 4 post-NEP. NGF ELISA from differentiated MEF media at 4 weeks post-NEP (n = 10). RT-qPCR analysis of neurotrophin mRNA at (F) 1 week (n = 4) and (G) 4 weeks (n = 6) post-NEP. Data expressed as mean ± SEM, *P < 0.05.

Article Snippet: Ascl1 , Brn2 , and Myt1l plasmids (backbone, pCAGGs) were constructed with GFP ( Ascl1 ), RFP ( Brn2 ), or CFP ( Myt1l ) by Applied Biological Materials Inc., Richmond, BC, Canada) as previously described.

Techniques: Expressing, Enzyme-linked Immunosorbent Assay, Quantitative RT-PCR

(A) Schematic diagram of TNT. (B) Confocal microscopic images showing three-plex in situ hybridization of Ascl1, Brn2, Myt1l, counterstained with DAPI. (C) RT–qPCR analysis of ABM gene expression in skin 24 h post-TNT. (n = 4), (D) Immunostaining showed TuJ1 fibers in skin. White dashed lines indicate epidermal and dermal junction. (E) Quantification of TuJ1+ fiber length per mm epidermis length. (n = 6) (F) Confocal microscopic images of skin showing co-localization (white) of FSP and TuJ1. (G) Quantification of TuJ1 and FSP positive cells per field of view. Data expressed as mean ± SEM (n = 3–4), *P < 0.05.

Journal: Nanomedicine : nanotechnology, biology, and medicine

Article Title: Neurogenic tissue nanotransfection in the management of cutaneous diabetic polyneuropathy

doi: 10.1016/j.nano.2020.102220

Figure Lengend Snippet: (A) Schematic diagram of TNT. (B) Confocal microscopic images showing three-plex in situ hybridization of Ascl1, Brn2, Myt1l, counterstained with DAPI. (C) RT–qPCR analysis of ABM gene expression in skin 24 h post-TNT. (n = 4), (D) Immunostaining showed TuJ1 fibers in skin. White dashed lines indicate epidermal and dermal junction. (E) Quantification of TuJ1+ fiber length per mm epidermis length. (n = 6) (F) Confocal microscopic images of skin showing co-localization (white) of FSP and TuJ1. (G) Quantification of TuJ1 and FSP positive cells per field of view. Data expressed as mean ± SEM (n = 3–4), *P < 0.05.

Article Snippet: Ascl1 , Brn2 , and Myt1l plasmids (backbone, pCAGGs) were constructed with GFP ( Ascl1 ), RFP ( Brn2 ), or CFP ( Myt1l ) by Applied Biological Materials Inc., Richmond, BC, Canada) as previously described.

Techniques: In Situ Hybridization, Quantitative RT-PCR, Gene Expression, Immunostaining