stem cellbanker Search Results


stem-cellbanker - gmp grade  (AMS Biotechnology)
96
AMS Biotechnology stem-cellbanker - gmp grade
Stem Cellbanker Gmp Grade, supplied by AMS Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/stem+cellbanker/STEM-CELLBANKER+-+GMP+Grade/custom%4011924%4027846293
Average 96 stars, based on 1 article reviews
stem-cellbanker - gmp grade - by Bioz Stars, 2026-10
96/100 stars
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stem-cellbanker  (TaKaRa)
96
TaKaRa stem-cellbanker
Stem Cellbanker, supplied by TaKaRa, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/stem+cellbanker/Stem-Cellbanker/custom%40stem-cellbanker%4010%2E64898%2F2026%2E08%2E25%2E746868
Average 96 stars, based on 1 article reviews
stem-cellbanker - by Bioz Stars, 2026-10
96/100 stars
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stem-cellbanker  (Cellvation Inc)
90
Cellvation Inc stem-cellbanker
Cell viability of adherent fibroblasts after freeze–thaw. (A) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) 24 h after thawing (n = 9). (B) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). (C) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 24 h after thawing (n = 9). (D) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). The white bars represent control non-frozen cells. The black bars represent cell preservation solutions including dimethyl sulfoxide <t>(DMSO).</t> The gray bars represent cell preservation solutions not containing DMSO.
Stem Cellbanker, supplied by Cellvation 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/stem+cellbanker/stem+cellbanker/pmc08579153-90-16-41
Average 90 stars, based on 1 article reviews
stem-cellbanker - by Bioz Stars, 2026-10
90/100 stars
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stem-cellbanker dmso free - gmp grade  (AMS Biotechnology)
96
AMS Biotechnology stem-cellbanker dmso free - gmp grade
Cell viability of adherent fibroblasts after freeze–thaw. (A) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) 24 h after thawing (n = 9). (B) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). (C) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 24 h after thawing (n = 9). (D) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). The white bars represent control non-frozen cells. The black bars represent cell preservation solutions including dimethyl sulfoxide <t>(DMSO).</t> The gray bars represent cell preservation solutions not containing DMSO.
Stem Cellbanker Dmso Free Gmp Grade, supplied by AMS Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/stem+cellbanker/STEM-CELLBANKER+DMSO+FREE+-+GMP+Grade/custom%4013926%4031144242
Average 96 stars, based on 1 article reviews
stem-cellbanker dmso free - gmp grade - by Bioz Stars, 2026-10
96/100 stars
  Buy from Supplier
stem-cellbanker  (STEMCELL Technologies Inc)
90
STEMCELL Technologies Inc stem-cellbanker
Cell viability of adherent fibroblasts after freeze–thaw. (A) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) 24 h after thawing (n = 9). (B) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). (C) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 24 h after thawing (n = 9). (D) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). The white bars represent control non-frozen cells. The black bars represent cell preservation solutions including dimethyl sulfoxide <t>(DMSO).</t> The gray bars represent cell preservation solutions not containing DMSO.
Stem Cellbanker, supplied by STEMCELL Technologies 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/stem+cellbanker/stem+cellbanker/pm21867427-39-25-29
Average 90 stars, based on 1 article reviews
stem-cellbanker - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
stem-cellbanker® gmp grade  (Corning Life Sciences)
90
Corning Life Sciences stem-cellbanker® gmp grade
Cell viability of adherent fibroblasts after freeze–thaw. (A) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) 24 h after thawing (n = 9). (B) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). (C) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 24 h after thawing (n = 9). (D) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). The white bars represent control non-frozen cells. The black bars represent cell preservation solutions including dimethyl sulfoxide <t>(DMSO).</t> The gray bars represent cell preservation solutions not containing DMSO.
Stem Cellbanker® Gmp Grade, supplied by Corning Life Sciences, 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/stem+cellbanker/stem+cellbanker++gmp+grade/pm40349487-52-5-21
Average 90 stars, based on 1 article reviews
stem-cellbanker® gmp grade - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
stem-cellbanker ex - gmp grade  (AMS Biotechnology)
N/A
STEM-CELLBANKER EX - GMP Grade (100ml)(formerly 11890EX)
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Image Search Results


Cell viability of adherent fibroblasts after freeze–thaw. (A) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) 24 h after thawing (n = 9). (B) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). (C) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 24 h after thawing (n = 9). (D) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). The white bars represent control non-frozen cells. The black bars represent cell preservation solutions including dimethyl sulfoxide (DMSO). The gray bars represent cell preservation solutions not containing DMSO.

Journal: Biochemistry and Biophysics Reports

Article Title: Freezing of cell sheets using a 3D freezer produces high cell viability after thawing

doi: 10.1016/j.bbrep.2021.101169

Figure Lengend Snippet: Cell viability of adherent fibroblasts after freeze–thaw. (A) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) 24 h after thawing (n = 9). (B) Adherent fibroblasts were frozen in five cell preservation solutions using a Program Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). (C) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 24 h after thawing (n = 9). (D) Adherent fibroblasts were frozen in five cell preservation solutions using a 3D Freezer and the viability of the adherent fibroblasts was evaluated using MTS 3 days after thawing (n = 9). The white bars represent control non-frozen cells. The black bars represent cell preservation solutions including dimethyl sulfoxide (DMSO). The gray bars represent cell preservation solutions not containing DMSO.

Article Snippet: The cell preservation solutions used were as follows: (a) STEM-CELLBANKER; (b) Bambanker hRM; (c) Bambanker; (d) STEM-CELLBANKER DMSO Free; (e) Cell Reservoir One (without DMSO); (f) Cryo Scarless DMSO Free; (g) Bambanker DMSO Free; (h) Stem Cell Keep; (i) ThelioKeep; (j) Cellvation; (k) Repro Cryo RM. (C) The hepatocyte growth factor (HGF) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3). (D) The transforming growth factor-β1 (TGF-β1) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3).

Techniques: Preserving, Control

Measurement of cooling temperature in cell preservation solutions in a 3D Freezer and a Program Freezer. Eleven cell preservation solutions were applied to three wells in six-well plates marked with numerical characters and frozen using a 3D Freezer or a Program Freezer. The cooling temperature was measured. The solid line indicates cell preservation solutions frozen using the 3D Freezer. The dotted line indicates cell preservation solutions frozen using the Program Freezer. The cell preservation solutions used were as follows: (A) STEM-CELLBANKER; (B) Bambanker hRM; (C) Bambanker; (D) STEM-CELLBANKER DMSO Free; (E) Cell Reservoir One (without DMSO); (F) Cryo Scarless DMSO Free; (G) Bambanker DMSO Free; (H) Stem Cell Keep; (I) ThelioKeep; (J) Cellvation; (K) Repro Cryo RM.

Journal: Biochemistry and Biophysics Reports

Article Title: Freezing of cell sheets using a 3D freezer produces high cell viability after thawing

doi: 10.1016/j.bbrep.2021.101169

Figure Lengend Snippet: Measurement of cooling temperature in cell preservation solutions in a 3D Freezer and a Program Freezer. Eleven cell preservation solutions were applied to three wells in six-well plates marked with numerical characters and frozen using a 3D Freezer or a Program Freezer. The cooling temperature was measured. The solid line indicates cell preservation solutions frozen using the 3D Freezer. The dotted line indicates cell preservation solutions frozen using the Program Freezer. The cell preservation solutions used were as follows: (A) STEM-CELLBANKER; (B) Bambanker hRM; (C) Bambanker; (D) STEM-CELLBANKER DMSO Free; (E) Cell Reservoir One (without DMSO); (F) Cryo Scarless DMSO Free; (G) Bambanker DMSO Free; (H) Stem Cell Keep; (I) ThelioKeep; (J) Cellvation; (K) Repro Cryo RM.

Article Snippet: The cell preservation solutions used were as follows: (a) STEM-CELLBANKER; (b) Bambanker hRM; (c) Bambanker; (d) STEM-CELLBANKER DMSO Free; (e) Cell Reservoir One (without DMSO); (f) Cryo Scarless DMSO Free; (g) Bambanker DMSO Free; (h) Stem Cell Keep; (i) ThelioKeep; (j) Cellvation; (k) Repro Cryo RM. (C) The hepatocyte growth factor (HGF) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3). (D) The transforming growth factor-β1 (TGF-β1) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3).

Techniques: Preserving

Cell viability and the ability of fibroblast sheets to secrete growth factors after freeze–thaw. (A) Morphological observation of fibroblast sheets before freezing and after thawing. A fibroblast sheet was prepared in a 12-well plate and soaked into Bambanker hRM (left side). The fibroblast sheet was frozen using a 3D Freezer, thawed and placed in phosphate-buffered saline (PBS) (right side). (B) The fibroblast sheets were frozen in 11 cell preservation solutions using a 3D Freezer and cultured for 3 days after thawing, and the cell viability of the fibroblast sheet was evaluated using (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) (n = 3). The cell preservation solutions used were as follows: (a) STEM-CELLBANKER; (b) Bambanker hRM; (c) Bambanker; (d) STEM-CELLBANKER DMSO Free; (e) Cell Reservoir One (without DMSO); (f) Cryo Scarless DMSO Free; (g) Bambanker DMSO Free; (h) Stem Cell Keep; (i) ThelioKeep; (j) Cellvation; (k) Repro Cryo RM. (C) The hepatocyte growth factor (HGF) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3). (D) The transforming growth factor-β1 (TGF-β1) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3). The white bars indicate control non-frozen cell sheets. The black bars indicate cell preservation solutions including dimethyl sulfoxide (DMSO). The gray bars indicate cell preservation solutions not containing DMSO.

Journal: Biochemistry and Biophysics Reports

Article Title: Freezing of cell sheets using a 3D freezer produces high cell viability after thawing

doi: 10.1016/j.bbrep.2021.101169

Figure Lengend Snippet: Cell viability and the ability of fibroblast sheets to secrete growth factors after freeze–thaw. (A) Morphological observation of fibroblast sheets before freezing and after thawing. A fibroblast sheet was prepared in a 12-well plate and soaked into Bambanker hRM (left side). The fibroblast sheet was frozen using a 3D Freezer, thawed and placed in phosphate-buffered saline (PBS) (right side). (B) The fibroblast sheets were frozen in 11 cell preservation solutions using a 3D Freezer and cultured for 3 days after thawing, and the cell viability of the fibroblast sheet was evaluated using (3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium) (MTS) (n = 3). The cell preservation solutions used were as follows: (a) STEM-CELLBANKER; (b) Bambanker hRM; (c) Bambanker; (d) STEM-CELLBANKER DMSO Free; (e) Cell Reservoir One (without DMSO); (f) Cryo Scarless DMSO Free; (g) Bambanker DMSO Free; (h) Stem Cell Keep; (i) ThelioKeep; (j) Cellvation; (k) Repro Cryo RM. (C) The hepatocyte growth factor (HGF) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3). (D) The transforming growth factor-β1 (TGF-β1) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3). The white bars indicate control non-frozen cell sheets. The black bars indicate cell preservation solutions including dimethyl sulfoxide (DMSO). The gray bars indicate cell preservation solutions not containing DMSO.

Article Snippet: The cell preservation solutions used were as follows: (a) STEM-CELLBANKER; (b) Bambanker hRM; (c) Bambanker; (d) STEM-CELLBANKER DMSO Free; (e) Cell Reservoir One (without DMSO); (f) Cryo Scarless DMSO Free; (g) Bambanker DMSO Free; (h) Stem Cell Keep; (i) ThelioKeep; (j) Cellvation; (k) Repro Cryo RM. (C) The hepatocyte growth factor (HGF) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3). (D) The transforming growth factor-β1 (TGF-β1) concentration was analyzed in the supernatant of fibroblast sheets cultured for 3 days after thawing (n = 3).

Techniques: Saline, Preserving, Cell Culture, Concentration Assay, Control