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human immortalized corneal endothelial cell line b4g12  (Creative Bioarray Inc)

 
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    Creative Bioarray Inc human immortalized corneal endothelial cell line b4g12
    Human Immortalized Corneal Endothelial Cell Line B4g12, supplied by Creative Bioarray 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/human+corneal+endothelial+cells+line+b4g12/human+corneal+endothelial+cell+line+b4g12/pm37482117-47-4-13
    Average 90 stars, based on 1 article reviews
    human immortalized corneal endothelial cell line b4g12 - by Bioz Stars, 2026-09
    90/100 stars

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    Article Title: Type 2 Diabetes Mellitus Makes Corneal Endothelial Cells Vulnerable to Ultraviolet A-Induced Oxidative Damage Via Decreased DJ-1/Nrf2/NQO1 Pathway
    Article Snippet: The human corneal endothelial cells line B4G12 (HCECs) were purchased from Creative Bioarray (Shirley, NY, USA).



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    Evaluation of MXF-HA efficacy using a rabbit model. ( A ) MXF-HA is inserted into the anterior chamber through a corneal incision while folded by forceps (yellow arrow). The unfolded circular MXF-HA is visible inside the anterior chamber immediately after implantation (white arrows indicate the margin of MXF-HA). ( B ) The implanted MXF-HA was visible on day 1 after surgery (white arrows). However, no visible MXF-HA structures were detected on days 7 and 14 after the surgery. Control is the contralateral eye without MXF-HA insertion. ( C ) MXF concentration was measured using aqueous humor collection. MXF concentrations in aqueous humor were maintained above 8 μg/mL for 5 days. ( D ) The intraocular pressure of MXF-HA-implanted eyes was not significantly different from that of the contralateral control eyes and was maintained within the normal range. ( E ) Eyeballs were harvested and imaged using optical coherence tomography (OCT). Normal corneal structure and thickness were maintained in both MXF-HA and control eyes. Histology (hematoxylin and eosin [H&E] staining) showed normal cellularity in all corneal layers without signs of inflammation in both MXF-HA and control eyes. ( F ) Specular microscopy revealed normal density and morphology of corneal <t>endothelial</t> cells in both MXF-HA and control eyes. *p < 0.05, **p < 0.01, ***p < 0.001.
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    Evaluation of MXF-HA efficacy using a rabbit model. ( A ) MXF-HA is inserted into the anterior chamber through a corneal incision while folded by forceps (yellow arrow). The unfolded circular MXF-HA is visible inside the anterior chamber immediately after implantation (white arrows indicate the margin of MXF-HA). ( B ) The implanted MXF-HA was visible on day 1 after surgery (white arrows). However, no visible MXF-HA structures were detected on days 7 and 14 after the surgery. Control is the contralateral eye without MXF-HA insertion. ( C ) MXF concentration was measured using aqueous humor collection. MXF concentrations in aqueous humor were maintained above 8 μg/mL for 5 days. ( D ) The intraocular pressure of MXF-HA-implanted eyes was not significantly different from that of the contralateral control eyes and was maintained within the normal range. ( E ) Eyeballs were harvested and imaged using optical coherence tomography (OCT). Normal corneal structure and thickness were maintained in both MXF-HA and control eyes. Histology (hematoxylin and eosin [H&E] staining) showed normal cellularity in all corneal layers without signs of inflammation in both MXF-HA and control eyes. ( F ) Specular microscopy revealed normal density and morphology of corneal <t>endothelial</t> cells in both MXF-HA and control eyes. *p < 0.05, **p < 0.01, ***p < 0.001.
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    Evaluation of MXF-HA efficacy using a rabbit model. ( A ) MXF-HA is inserted into the anterior chamber through a corneal incision while folded by forceps (yellow arrow). The unfolded circular MXF-HA is visible inside the anterior chamber immediately after implantation (white arrows indicate the margin of MXF-HA). ( B ) The implanted MXF-HA was visible on day 1 after surgery (white arrows). However, no visible MXF-HA structures were detected on days 7 and 14 after the surgery. Control is the contralateral eye without MXF-HA insertion. ( C ) MXF concentration was measured using aqueous humor collection. MXF concentrations in aqueous humor were maintained above 8 μg/mL for 5 days. ( D ) The intraocular pressure of MXF-HA-implanted eyes was not significantly different from that of the contralateral control eyes and was maintained within the normal range. ( E ) Eyeballs were harvested and imaged using optical coherence tomography (OCT). Normal corneal structure and thickness were maintained in both MXF-HA and control eyes. Histology (hematoxylin and eosin [H&E] staining) showed normal cellularity in all corneal layers without signs of inflammation in both MXF-HA and control eyes. ( F ) Specular microscopy revealed normal density and morphology of corneal <t>endothelial</t> cells in both MXF-HA and control eyes. *p < 0.05, **p < 0.01, ***p < 0.001.
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    Image Search Results


    Evaluation of MXF-HA efficacy using a rabbit model. ( A ) MXF-HA is inserted into the anterior chamber through a corneal incision while folded by forceps (yellow arrow). The unfolded circular MXF-HA is visible inside the anterior chamber immediately after implantation (white arrows indicate the margin of MXF-HA). ( B ) The implanted MXF-HA was visible on day 1 after surgery (white arrows). However, no visible MXF-HA structures were detected on days 7 and 14 after the surgery. Control is the contralateral eye without MXF-HA insertion. ( C ) MXF concentration was measured using aqueous humor collection. MXF concentrations in aqueous humor were maintained above 8 μg/mL for 5 days. ( D ) The intraocular pressure of MXF-HA-implanted eyes was not significantly different from that of the contralateral control eyes and was maintained within the normal range. ( E ) Eyeballs were harvested and imaged using optical coherence tomography (OCT). Normal corneal structure and thickness were maintained in both MXF-HA and control eyes. Histology (hematoxylin and eosin [H&E] staining) showed normal cellularity in all corneal layers without signs of inflammation in both MXF-HA and control eyes. ( F ) Specular microscopy revealed normal density and morphology of corneal endothelial cells in both MXF-HA and control eyes. *p < 0.05, **p < 0.01, ***p < 0.001.

    Journal: Scientific Reports

    Article Title: Moxifloxacin releasing intraocular implant based on a cross-linked hyaluronic acid membrane

    doi: 10.1038/s41598-021-03605-0

    Figure Lengend Snippet: Evaluation of MXF-HA efficacy using a rabbit model. ( A ) MXF-HA is inserted into the anterior chamber through a corneal incision while folded by forceps (yellow arrow). The unfolded circular MXF-HA is visible inside the anterior chamber immediately after implantation (white arrows indicate the margin of MXF-HA). ( B ) The implanted MXF-HA was visible on day 1 after surgery (white arrows). However, no visible MXF-HA structures were detected on days 7 and 14 after the surgery. Control is the contralateral eye without MXF-HA insertion. ( C ) MXF concentration was measured using aqueous humor collection. MXF concentrations in aqueous humor were maintained above 8 μg/mL for 5 days. ( D ) The intraocular pressure of MXF-HA-implanted eyes was not significantly different from that of the contralateral control eyes and was maintained within the normal range. ( E ) Eyeballs were harvested and imaged using optical coherence tomography (OCT). Normal corneal structure and thickness were maintained in both MXF-HA and control eyes. Histology (hematoxylin and eosin [H&E] staining) showed normal cellularity in all corneal layers without signs of inflammation in both MXF-HA and control eyes. ( F ) Specular microscopy revealed normal density and morphology of corneal endothelial cells in both MXF-HA and control eyes. *p < 0.05, **p < 0.01, ***p < 0.001.

    Article Snippet: The corneal endothelial safety of MXF-HA was analyzed using human corneal endothelial cell line (B4G12, Creative Bioarray, Shirley, NY, USA).

    Techniques: Control, Concentration Assay, Tomography, Staining, Microscopy

    Comparison of corneal endothelial cell density and morphology between MXF-HA-implanted and control eyes in rabbits. Data was described as mean ± standard deviation, and p values were calculated using the Mann–Whitney test.

    Journal: Scientific Reports

    Article Title: Moxifloxacin releasing intraocular implant based on a cross-linked hyaluronic acid membrane

    doi: 10.1038/s41598-021-03605-0

    Figure Lengend Snippet: Comparison of corneal endothelial cell density and morphology between MXF-HA-implanted and control eyes in rabbits. Data was described as mean ± standard deviation, and p values were calculated using the Mann–Whitney test.

    Article Snippet: The corneal endothelial safety of MXF-HA was analyzed using human corneal endothelial cell line (B4G12, Creative Bioarray, Shirley, NY, USA).

    Techniques: Comparison, Control, Standard Deviation