cell specific culturing medium Search Results


carboxyphenol ba  (Chem Impex International)
94
Chem Impex International carboxyphenol ba
Carboxyphenol Ba, supplied by Chem Impex International, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/carboxyphenol ba/product/Chem Impex International
Average 94 stars, based on 1 article reviews
carboxyphenol ba - by Bioz Stars, 2026-03
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mouse aortic endothelial cell line procell cp-m075  (Procell Inc)
90
Procell Inc mouse aortic endothelial cell line procell cp-m075
Mouse Aortic Endothelial Cell Line Procell Cp M075, supplied by Procell 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/mouse aortic endothelial cell line procell cp-m075/product/Procell Inc
Average 90 stars, based on 1 article reviews
mouse aortic endothelial cell line procell cp-m075 - by Bioz Stars, 2026-03
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specific epithelial culture medium  (Pro-cell Co Ltd)
90
Pro-cell Co Ltd specific epithelial culture medium
Specific Epithelial Culture Medium, supplied by Pro-cell Co Ltd, 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/specific epithelial culture medium/product/Pro-cell Co Ltd
Average 90 stars, based on 1 article reviews
specific epithelial culture medium - by Bioz Stars, 2026-03
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nb4 cell-specific culture medium  (Procell Inc)
90
Procell Inc nb4 cell-specific culture medium
SiSTAT4 decreased STAT4 expression, while overexpressed STAT4 did conversely in transfected HL60 and <t>NB4</t> cells. (a) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was used as the loading gene. (b) The expression of STAT4 in HL60 cells after transfection was examined by Western blot, and GAPDH was adopted as the internal control. (c) The expression of STAT4 in NB4 cells after transfection was examined by qPCR, and GAPDH was employed as a loading gene. (d) The expression of STAT4 in NB4 cells after transfection was examined by Western blot, and GAPDH was utilized as the internal control. (e) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was harnessed as the reference gene. (f) The expression of STAT4 in HL60 cells after transfection was measured by Western blot, and GAPDH was exploited as the internal control. (g) The expression of STAT4 in NB4 cells after transfection was quantified by qPCR, and GAPDH was applied as the reference gene. (h) The expression of STAT4 in NB4 cells after transfection was determined by Western blot, and GAPDH was adopted as the loading control. *** P < 0.001 vs siNC; ^^^ P < 0.001 vs NC (NC: negative control, siSTAT4: siRNA targeting STAT4, siNC: negative control of siSTAT4).
Nb4 Cell Specific Culture Medium, supplied by Procell 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/nb4 cell-specific culture medium/product/Procell Inc
Average 90 stars, based on 1 article reviews
nb4 cell-specific culture medium - by Bioz Stars, 2026-03
90/100 stars
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cell specific culture-medium icell-h091001b  (iCell Gene Therapeutics)
90
iCell Gene Therapeutics cell specific culture-medium icell-h091001b
SiSTAT4 decreased STAT4 expression, while overexpressed STAT4 did conversely in transfected HL60 and <t>NB4</t> cells. (a) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was used as the loading gene. (b) The expression of STAT4 in HL60 cells after transfection was examined by Western blot, and GAPDH was adopted as the internal control. (c) The expression of STAT4 in NB4 cells after transfection was examined by qPCR, and GAPDH was employed as a loading gene. (d) The expression of STAT4 in NB4 cells after transfection was examined by Western blot, and GAPDH was utilized as the internal control. (e) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was harnessed as the reference gene. (f) The expression of STAT4 in HL60 cells after transfection was measured by Western blot, and GAPDH was exploited as the internal control. (g) The expression of STAT4 in NB4 cells after transfection was quantified by qPCR, and GAPDH was applied as the reference gene. (h) The expression of STAT4 in NB4 cells after transfection was determined by Western blot, and GAPDH was adopted as the loading control. *** P < 0.001 vs siNC; ^^^ P < 0.001 vs NC (NC: negative control, siSTAT4: siRNA targeting STAT4, siNC: negative control of siSTAT4).
Cell Specific Culture Medium Icell H091001b, supplied by iCell Gene Therapeutics, 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/cell specific culture-medium icell-h091001b/product/iCell Gene Therapeutics
Average 90 stars, based on 1 article reviews
cell specific culture-medium icell-h091001b - by Bioz Stars, 2026-03
90/100 stars
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cell-specific culture medium  (FLUIGENT Inc)
90
FLUIGENT Inc cell-specific culture medium
SiSTAT4 decreased STAT4 expression, while overexpressed STAT4 did conversely in transfected HL60 and <t>NB4</t> cells. (a) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was used as the loading gene. (b) The expression of STAT4 in HL60 cells after transfection was examined by Western blot, and GAPDH was adopted as the internal control. (c) The expression of STAT4 in NB4 cells after transfection was examined by qPCR, and GAPDH was employed as a loading gene. (d) The expression of STAT4 in NB4 cells after transfection was examined by Western blot, and GAPDH was utilized as the internal control. (e) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was harnessed as the reference gene. (f) The expression of STAT4 in HL60 cells after transfection was measured by Western blot, and GAPDH was exploited as the internal control. (g) The expression of STAT4 in NB4 cells after transfection was quantified by qPCR, and GAPDH was applied as the reference gene. (h) The expression of STAT4 in NB4 cells after transfection was determined by Western blot, and GAPDH was adopted as the loading control. *** P < 0.001 vs siNC; ^^^ P < 0.001 vs NC (NC: negative control, siSTAT4: siRNA targeting STAT4, siNC: negative control of siSTAT4).
Cell Specific Culture Medium, supplied by FLUIGENT 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/cell-specific culture medium/product/FLUIGENT Inc
Average 90 stars, based on 1 article reviews
cell-specific culture medium - by Bioz Stars, 2026-03
90/100 stars
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hrmecs-specific endothelial cell culture medium (ecm) kit  (ScienCell)
90
ScienCell hrmecs-specific endothelial cell culture medium (ecm) kit
SiSTAT4 decreased STAT4 expression, while overexpressed STAT4 did conversely in transfected HL60 and <t>NB4</t> cells. (a) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was used as the loading gene. (b) The expression of STAT4 in HL60 cells after transfection was examined by Western blot, and GAPDH was adopted as the internal control. (c) The expression of STAT4 in NB4 cells after transfection was examined by qPCR, and GAPDH was employed as a loading gene. (d) The expression of STAT4 in NB4 cells after transfection was examined by Western blot, and GAPDH was utilized as the internal control. (e) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was harnessed as the reference gene. (f) The expression of STAT4 in HL60 cells after transfection was measured by Western blot, and GAPDH was exploited as the internal control. (g) The expression of STAT4 in NB4 cells after transfection was quantified by qPCR, and GAPDH was applied as the reference gene. (h) The expression of STAT4 in NB4 cells after transfection was determined by Western blot, and GAPDH was adopted as the loading control. *** P < 0.001 vs siNC; ^^^ P < 0.001 vs NC (NC: negative control, siSTAT4: siRNA targeting STAT4, siNC: negative control of siSTAT4).
Hrmecs Specific Endothelial Cell Culture Medium (Ecm) Kit, supplied by ScienCell, 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/hrmecs-specific endothelial cell culture medium (ecm) kit/product/ScienCell
Average 90 stars, based on 1 article reviews
hrmecs-specific endothelial cell culture medium (ecm) kit - by Bioz Stars, 2026-03
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Image Search Results


SiSTAT4 decreased STAT4 expression, while overexpressed STAT4 did conversely in transfected HL60 and NB4 cells. (a) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was used as the loading gene. (b) The expression of STAT4 in HL60 cells after transfection was examined by Western blot, and GAPDH was adopted as the internal control. (c) The expression of STAT4 in NB4 cells after transfection was examined by qPCR, and GAPDH was employed as a loading gene. (d) The expression of STAT4 in NB4 cells after transfection was examined by Western blot, and GAPDH was utilized as the internal control. (e) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was harnessed as the reference gene. (f) The expression of STAT4 in HL60 cells after transfection was measured by Western blot, and GAPDH was exploited as the internal control. (g) The expression of STAT4 in NB4 cells after transfection was quantified by qPCR, and GAPDH was applied as the reference gene. (h) The expression of STAT4 in NB4 cells after transfection was determined by Western blot, and GAPDH was adopted as the loading control. *** P < 0.001 vs siNC; ^^^ P < 0.001 vs NC (NC: negative control, siSTAT4: siRNA targeting STAT4, siNC: negative control of siSTAT4).

Journal: Open Medicine

Article Title: High STAT4 expression correlates with poor prognosis in acute myeloid leukemia and facilitates disease progression by upregulating VEGFA expression

doi: 10.1515/med-2023-0840

Figure Lengend Snippet: SiSTAT4 decreased STAT4 expression, while overexpressed STAT4 did conversely in transfected HL60 and NB4 cells. (a) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was used as the loading gene. (b) The expression of STAT4 in HL60 cells after transfection was examined by Western blot, and GAPDH was adopted as the internal control. (c) The expression of STAT4 in NB4 cells after transfection was examined by qPCR, and GAPDH was employed as a loading gene. (d) The expression of STAT4 in NB4 cells after transfection was examined by Western blot, and GAPDH was utilized as the internal control. (e) The expression of STAT4 in HL60 cells after transfection was examined by qPCR, and GAPDH was harnessed as the reference gene. (f) The expression of STAT4 in HL60 cells after transfection was measured by Western blot, and GAPDH was exploited as the internal control. (g) The expression of STAT4 in NB4 cells after transfection was quantified by qPCR, and GAPDH was applied as the reference gene. (h) The expression of STAT4 in NB4 cells after transfection was determined by Western blot, and GAPDH was adopted as the loading control. *** P < 0.001 vs siNC; ^^^ P < 0.001 vs NC (NC: negative control, siSTAT4: siRNA targeting STAT4, siNC: negative control of siSTAT4).

Article Snippet: NB4 cells were seeded within NB4 cell-specific culture medium (CM-0676; Procell).

Techniques: Expressing, Transfection, Western Blot, Negative Control

STAT4 silencing decreased the viability, while overexpressed STAT4 did conversely in transfected AML cells. (a–d) The viability of HL60 and NB4 cells after transfection was examined by MTT assay. * P < 0.05, *** P < 0.001 vs siNC; ^ P < 0.05, ^^^ P < 0.001 vs NC.

Journal: Open Medicine

Article Title: High STAT4 expression correlates with poor prognosis in acute myeloid leukemia and facilitates disease progression by upregulating VEGFA expression

doi: 10.1515/med-2023-0840

Figure Lengend Snippet: STAT4 silencing decreased the viability, while overexpressed STAT4 did conversely in transfected AML cells. (a–d) The viability of HL60 and NB4 cells after transfection was examined by MTT assay. * P < 0.05, *** P < 0.001 vs siNC; ^ P < 0.05, ^^^ P < 0.001 vs NC.

Article Snippet: NB4 cells were seeded within NB4 cell-specific culture medium (CM-0676; Procell).

Techniques: Transfection, MTT Assay

STAT4 silencing decreased Bcl-2 level, yet increased apoptosis and Bax level in AML cells, while overexpressed STAT4 did conversely. (a and b) The apoptosis of HL60 and NB4 cells after transfection was examined by flow cytometry. (c) The expressions of Bcl-2 and Bax in HL60 cells after transfection were quantified by qPCR, and GAPDH was used as the reference gene. (d) The expressions of Bcl-2 and Bax in HL60 cells after transfection were detected by Western blot, and GAPDH was used as the loading control. (e) The expressions of Bcl-2 and Bax in NB4 cells after transfection were measured by qPCR, and GAPDH was used as the reference gene. (f) The expressions of Bcl-2 and Bax in NB4 cells after transfection were examined by Western blot, and GAPDH was used as the internal control. *** P < 0.001 vs siNC; ^^^ P < P < 0.001 vs NC.

Journal: Open Medicine

Article Title: High STAT4 expression correlates with poor prognosis in acute myeloid leukemia and facilitates disease progression by upregulating VEGFA expression

doi: 10.1515/med-2023-0840

Figure Lengend Snippet: STAT4 silencing decreased Bcl-2 level, yet increased apoptosis and Bax level in AML cells, while overexpressed STAT4 did conversely. (a and b) The apoptosis of HL60 and NB4 cells after transfection was examined by flow cytometry. (c) The expressions of Bcl-2 and Bax in HL60 cells after transfection were quantified by qPCR, and GAPDH was used as the reference gene. (d) The expressions of Bcl-2 and Bax in HL60 cells after transfection were detected by Western blot, and GAPDH was used as the loading control. (e) The expressions of Bcl-2 and Bax in NB4 cells after transfection were measured by qPCR, and GAPDH was used as the reference gene. (f) The expressions of Bcl-2 and Bax in NB4 cells after transfection were examined by Western blot, and GAPDH was used as the internal control. *** P < 0.001 vs siNC; ^^^ P < P < 0.001 vs NC.

Article Snippet: NB4 cells were seeded within NB4 cell-specific culture medium (CM-0676; Procell).

Techniques: Transfection, Flow Cytometry, Western Blot

STAT4 silencing decreased the angiogenesis and VEGFA level, while overexpressed STAT4 did conversely. (a and b) The angiogenesis of HL60 and NB4 cells after transfection was examined by tube formation assay under ×100 magnification. (c) The expressions of STAT4 and VEGFA in HL60 cells after transfection were tested by qPCR, and GAPDH was used as the reference gene. (d) The expressions of STAT4 and VEGFA in HL60 cells after transfection were determined by Western blot, and GAPDH was adopted as the internal control. (e) The expressions of STAT4 and VEGFA in NB4 cells after transfection were assayed by qPCR, and GAPDH was utilized as the reference gene. (f) The expressions of STAT4 and VEGFA in NB4 cells after transfection were measured by Western blot, and GAPDH was exploited as the loading control. *** P < 0.001 vs siNC; ^^^ P < 0.001 vs NC (VEGFA: vascular endothelial growth factor A).

Journal: Open Medicine

Article Title: High STAT4 expression correlates with poor prognosis in acute myeloid leukemia and facilitates disease progression by upregulating VEGFA expression

doi: 10.1515/med-2023-0840

Figure Lengend Snippet: STAT4 silencing decreased the angiogenesis and VEGFA level, while overexpressed STAT4 did conversely. (a and b) The angiogenesis of HL60 and NB4 cells after transfection was examined by tube formation assay under ×100 magnification. (c) The expressions of STAT4 and VEGFA in HL60 cells after transfection were tested by qPCR, and GAPDH was used as the reference gene. (d) The expressions of STAT4 and VEGFA in HL60 cells after transfection were determined by Western blot, and GAPDH was adopted as the internal control. (e) The expressions of STAT4 and VEGFA in NB4 cells after transfection were assayed by qPCR, and GAPDH was utilized as the reference gene. (f) The expressions of STAT4 and VEGFA in NB4 cells after transfection were measured by Western blot, and GAPDH was exploited as the loading control. *** P < 0.001 vs siNC; ^^^ P < 0.001 vs NC (VEGFA: vascular endothelial growth factor A).

Article Snippet: NB4 cells were seeded within NB4 cell-specific culture medium (CM-0676; Procell).

Techniques: Transfection, Tube Formation Assay, Western Blot

VEGFA silencing counteracted the effects of overexpressed STAT4 on promoting the viability and angiogenesis as well as inhibiting the apoptosis of AML cells. (a and b) The viability of HL60 and NB4 cells after transfection was examined by MTT assay. (c and d) The angiogenesis of HL60 and NB4 cells after transfection was determined by tube formation assay under ×100 magnification. (e and f) The apoptosis of HL60 and NB4 cells after transfection was tested by flow cytometry. * P < 0.05, ** P < 0.01 , *** P < 0.001 vs NC + vector; ^ P < 0.05, ^^ P < 0.01, ^^^ P < 0.001 vs STAT4 + vector; # P < 0.05, ## P < 0.01, ### P < 0.001 vs NC + siVEGFA (siVEGFA: siRNA targeting VEGFA, vector: negative control for siVEGFA).

Journal: Open Medicine

Article Title: High STAT4 expression correlates with poor prognosis in acute myeloid leukemia and facilitates disease progression by upregulating VEGFA expression

doi: 10.1515/med-2023-0840

Figure Lengend Snippet: VEGFA silencing counteracted the effects of overexpressed STAT4 on promoting the viability and angiogenesis as well as inhibiting the apoptosis of AML cells. (a and b) The viability of HL60 and NB4 cells after transfection was examined by MTT assay. (c and d) The angiogenesis of HL60 and NB4 cells after transfection was determined by tube formation assay under ×100 magnification. (e and f) The apoptosis of HL60 and NB4 cells after transfection was tested by flow cytometry. * P < 0.05, ** P < 0.01 , *** P < 0.001 vs NC + vector; ^ P < 0.05, ^^ P < 0.01, ^^^ P < 0.001 vs STAT4 + vector; # P < 0.05, ## P < 0.01, ### P < 0.001 vs NC + siVEGFA (siVEGFA: siRNA targeting VEGFA, vector: negative control for siVEGFA).

Article Snippet: NB4 cells were seeded within NB4 cell-specific culture medium (CM-0676; Procell).

Techniques: Transfection, MTT Assay, Tube Formation Assay, Flow Cytometry, Plasmid Preparation, Negative Control