hichondroxl™ Search Results


hichondroxltm chondrocyte differentiation medium al523  (HiMedia Laboratories)
90
HiMedia Laboratories hichondroxltm chondrocyte differentiation medium al523
Hichondroxltm Chondrocyte Differentiation Medium Al523, supplied by HiMedia Laboratories, 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/hichondroxl%E2%84%A2/osteogenic+media/pmc10216643-54-28-33
Average 90 stars, based on 1 article reviews
hichondroxltm chondrocyte differentiation medium al523 - by Bioz Stars, 2026-10
90/100 stars
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collagenase type ii  (HiMedia Laboratories)
90
HiMedia Laboratories collagenase type ii
Morphology of cultured gingival cells from gingival tissue. The phase-contrast micrographs of gingival cells on day 1 ( a ), day 5 ( b ), day 7 ( c ) and day 18 ( d ) of primary culture show a small and large colony composed of densely distributed spindle (black arrow)-shaped cells. On day 15, the cells became flattened and surrounded by proliferating cells and reached confluency. Scale bar =50 μm. Original magnifications × 200. The morphology of the colony formation of HGMSCs represents that P2 cells stained with 1% crystal violet in methanol at day 15 of culture ( e, f ) show CFU-F colonies. Scale bar=20 cm. Original magnifications × 100. The proliferative effect of HGMSCs in vitro was measured by 3 H-thymidine incorporation assay. ( g ) The amount of incorporated 3 H-thymdine was measured after 24 h of culturing. Bars represent the mean±s.e.m. ( n =3). The flow cytometry analysis of HGMSCs, passage 3. ( h ) The expression is strongly positive for MSC-specific surface markers CD105, CD90, CD73 and negative for CD34 and CD45, compared with Isotype control, thus confirming their identity as MSCs. A histogram represents the expression level percentage. The mesenchymal-lineage differentiations of HGMSCs into osteocytes, adipocytes and chondrocytes. In vitro differentiated cells showed positive staining in the specific staining methods. ( i ) The deposition of a mineralized extracellular matrix (red) was seen after alizarin red staining. Adipogenic differentiation was confirmed by the Oil Red O staining of intracytoplasmic lipid droplets. The <t>chondrogenic</t> differentiation of MSCs with the positive staining of proteoglycans by Alcian blue; scale bar =20 μm. Original magnification × 200.
Collagenase Type Ii, supplied by HiMedia Laboratories, 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/hichondroxl%E2%84%A2/collagenase/pmc04892868-55-0-10
Average 90 stars, based on 1 article reviews
collagenase type ii - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier
chondrogenesis differentiation media hichondro xl kital523  (HiMedia Laboratories)
90
HiMedia Laboratories chondrogenesis differentiation media hichondro xl kital523
Morphology of cultured gingival cells from gingival tissue. The phase-contrast micrographs of gingival cells on day 1 ( a ), day 5 ( b ), day 7 ( c ) and day 18 ( d ) of primary culture show a small and large colony composed of densely distributed spindle (black arrow)-shaped cells. On day 15, the cells became flattened and surrounded by proliferating cells and reached confluency. Scale bar =50 μm. Original magnifications × 200. The morphology of the colony formation of HGMSCs represents that P2 cells stained with 1% crystal violet in methanol at day 15 of culture ( e, f ) show CFU-F colonies. Scale bar=20 cm. Original magnifications × 100. The proliferative effect of HGMSCs in vitro was measured by 3 H-thymidine incorporation assay. ( g ) The amount of incorporated 3 H-thymdine was measured after 24 h of culturing. Bars represent the mean±s.e.m. ( n =3). The flow cytometry analysis of HGMSCs, passage 3. ( h ) The expression is strongly positive for MSC-specific surface markers CD105, CD90, CD73 and negative for CD34 and CD45, compared with Isotype control, thus confirming their identity as MSCs. A histogram represents the expression level percentage. The mesenchymal-lineage differentiations of HGMSCs into osteocytes, adipocytes and chondrocytes. In vitro differentiated cells showed positive staining in the specific staining methods. ( i ) The deposition of a mineralized extracellular matrix (red) was seen after alizarin red staining. Adipogenic differentiation was confirmed by the Oil Red O staining of intracytoplasmic lipid droplets. The <t>chondrogenic</t> differentiation of MSCs with the positive staining of proteoglycans by Alcian blue; scale bar =20 μm. Original magnification × 200.
Chondrogenesis Differentiation Media Hichondro Xl Kital523, supplied by HiMedia Laboratories, 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/hichondroxl%E2%84%A2/chondrogenesis+differentiation+media+hichondro+xl+kital523/pm39874919-80-11-17
Average 90 stars, based on 1 article reviews
chondrogenesis differentiation media hichondro xl kital523 - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

Image Search Results


Morphology of cultured gingival cells from gingival tissue. The phase-contrast micrographs of gingival cells on day 1 ( a ), day 5 ( b ), day 7 ( c ) and day 18 ( d ) of primary culture show a small and large colony composed of densely distributed spindle (black arrow)-shaped cells. On day 15, the cells became flattened and surrounded by proliferating cells and reached confluency. Scale bar =50 μm. Original magnifications × 200. The morphology of the colony formation of HGMSCs represents that P2 cells stained with 1% crystal violet in methanol at day 15 of culture ( e, f ) show CFU-F colonies. Scale bar=20 cm. Original magnifications × 100. The proliferative effect of HGMSCs in vitro was measured by 3 H-thymidine incorporation assay. ( g ) The amount of incorporated 3 H-thymdine was measured after 24 h of culturing. Bars represent the mean±s.e.m. ( n =3). The flow cytometry analysis of HGMSCs, passage 3. ( h ) The expression is strongly positive for MSC-specific surface markers CD105, CD90, CD73 and negative for CD34 and CD45, compared with Isotype control, thus confirming their identity as MSCs. A histogram represents the expression level percentage. The mesenchymal-lineage differentiations of HGMSCs into osteocytes, adipocytes and chondrocytes. In vitro differentiated cells showed positive staining in the specific staining methods. ( i ) The deposition of a mineralized extracellular matrix (red) was seen after alizarin red staining. Adipogenic differentiation was confirmed by the Oil Red O staining of intracytoplasmic lipid droplets. The chondrogenic differentiation of MSCs with the positive staining of proteoglycans by Alcian blue; scale bar =20 μm. Original magnification × 200.

Journal: Experimental & Molecular Medicine

Article Title: Differentiation of human gingival mesenchymal stem cells into neuronal lineages in 3D bioconjugated injectable protein hydrogel construct for the management of neuronal disorder

doi: 10.1038/emm.2015.113

Figure Lengend Snippet: Morphology of cultured gingival cells from gingival tissue. The phase-contrast micrographs of gingival cells on day 1 ( a ), day 5 ( b ), day 7 ( c ) and day 18 ( d ) of primary culture show a small and large colony composed of densely distributed spindle (black arrow)-shaped cells. On day 15, the cells became flattened and surrounded by proliferating cells and reached confluency. Scale bar =50 μm. Original magnifications × 200. The morphology of the colony formation of HGMSCs represents that P2 cells stained with 1% crystal violet in methanol at day 15 of culture ( e, f ) show CFU-F colonies. Scale bar=20 cm. Original magnifications × 100. The proliferative effect of HGMSCs in vitro was measured by 3 H-thymidine incorporation assay. ( g ) The amount of incorporated 3 H-thymdine was measured after 24 h of culturing. Bars represent the mean±s.e.m. ( n =3). The flow cytometry analysis of HGMSCs, passage 3. ( h ) The expression is strongly positive for MSC-specific surface markers CD105, CD90, CD73 and negative for CD34 and CD45, compared with Isotype control, thus confirming their identity as MSCs. A histogram represents the expression level percentage. The mesenchymal-lineage differentiations of HGMSCs into osteocytes, adipocytes and chondrocytes. In vitro differentiated cells showed positive staining in the specific staining methods. ( i ) The deposition of a mineralized extracellular matrix (red) was seen after alizarin red staining. Adipogenic differentiation was confirmed by the Oil Red O staining of intracytoplasmic lipid droplets. The chondrogenic differentiation of MSCs with the positive staining of proteoglycans by Alcian blue; scale bar =20 μm. Original magnification × 200.

Article Snippet: Collagenase Type II HiChondroXL Chondrogenic differentiation media were obtained from HiMedia (Mumbai, India).

Techniques: Cell Culture, Staining, In Vitro, Thymidine Incorporation Assay, Flow Cytometry, Expressing, Control