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rabbit monoclonal anti mafa d2z6n  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc rabbit monoclonal anti mafa d2z6n
    Rabbit Monoclonal Anti Mafa D2z6n, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 95/100, based on 37 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mafa/MAFA+Rabbit+mAb/pmc13049674-2-0-5
    Average 95 stars, based on 37 article reviews
    rabbit monoclonal anti mafa d2z6n - by Bioz Stars, 2026-09
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    Related Articles

    Blocking Assay:

    Article Title: Pancreatic β cell interleukin-22 receptor subunit alpha 1 deficiency impairs β cell function in type 2 diabetes via cytochrome b5 reductase 3.
    Article Snippet: 5X protein loading buffer (Beyotime Biotechnology, P0286) was added to the residual supernatants and boiled for 20 min. About 30mg of total protein was subjected to sodium dodecyl-sulfate polyacrylamide gel (SDS-PAGE) electrophoresis, and transferred to nitrocellulose membranes (Millipore, Billerica, MA, USA). .. After blocking with 5% BSA for 1.5h, membranes were incubated overnight at 4 C with the following primary antibodies at a dilution of 1:1000: b-Actin (Cell Signaling Technology, 4970), STAT3 (Cell Signaling Technology, 4904), p-STAT3Tyr705 (Cell Signaling Technology, 9131), IL22RA1 (Invitrogen, PA5-19987), c-Jun (Cell Signaling Technology, 9165), p-JunSer73 (Cell Signaling Technology, 9164), CYB5R3 (Proteintech, 10894-1- AP), OXPHOS (Abcam, ab110413), MAFA (Cell Signaling Technology, 79737), PDX1 (Abcam, ab47308), NKX6.1 (Cell Signaling Technology, 54551). .. Next day, membranes were incubated with secondary antibodies at room temperature for 1 h. HRP peroxidase-conjugated anti-mouse IgG (Cell Signaling Technology, 7076) and HRP peroxidase-conjugated anti-rabbit IgG (Cell Signaling Technology, 7074).

    Article Title: Pancreatic β cell interleukin-22 receptor subunit alpha 1 deficiency impairs β cell function in type 2 diabetes via cytochrome b5 reductase 3.
    Article Snippet: .. Antigen retrieval was carried out by boiling in Tris-EDTA buffer or citrate buffer for microwaving 10 min. After cooling to room temperature, sections were covered in blocking buffer (5% donkey serum in PBS) for 1 h. Primary antibodies were applied at a dilution of 1:400 for INSULIN (Cell Signaling Technology, 8138), 1:400 for GLUCAGON (Cell Signaling Technology, 2760), 1:50 for IL22RA1 (R&D SYSTEM, 496514), 1:100 for CYB5R3 (Proteintech, 10894-1-AP), 1:100 for MAFA (Cell Signaling Technology, 79737), 1:100 for PDX1 (Abcam, ab47308), 1:100 for NKX6.1 (Cell Signaling Technology, 54551), and 1:400 for GFP (Abcam, ab13970) overnight at 4 C. Next day, sections were washed in PBS for three times and incubated with Alexa Fluor conjugated secondary antibodies (Abcam, ab150106; Abcam, ab150073; Invitrogen, A21208) at a dilution of 1:400 for 1 h. Nuclei were counterstained with DAPI (Beyotime, C1002) at a dilution of 1:5000 for 5 min. .. Images were acquired using a Leica microscope (Leica, DM4B) and scanned by AKOYA Vectra Polaris.

    Incubation:

    Article Title: Pancreatic β cell interleukin-22 receptor subunit alpha 1 deficiency impairs β cell function in type 2 diabetes via cytochrome b5 reductase 3.
    Article Snippet: 5X protein loading buffer (Beyotime Biotechnology, P0286) was added to the residual supernatants and boiled for 20 min. About 30mg of total protein was subjected to sodium dodecyl-sulfate polyacrylamide gel (SDS-PAGE) electrophoresis, and transferred to nitrocellulose membranes (Millipore, Billerica, MA, USA). .. After blocking with 5% BSA for 1.5h, membranes were incubated overnight at 4 C with the following primary antibodies at a dilution of 1:1000: b-Actin (Cell Signaling Technology, 4970), STAT3 (Cell Signaling Technology, 4904), p-STAT3Tyr705 (Cell Signaling Technology, 9131), IL22RA1 (Invitrogen, PA5-19987), c-Jun (Cell Signaling Technology, 9165), p-JunSer73 (Cell Signaling Technology, 9164), CYB5R3 (Proteintech, 10894-1- AP), OXPHOS (Abcam, ab110413), MAFA (Cell Signaling Technology, 79737), PDX1 (Abcam, ab47308), NKX6.1 (Cell Signaling Technology, 54551). .. Next day, membranes were incubated with secondary antibodies at room temperature for 1 h. HRP peroxidase-conjugated anti-mouse IgG (Cell Signaling Technology, 7076) and HRP peroxidase-conjugated anti-rabbit IgG (Cell Signaling Technology, 7074).

    Article Title: Pancreatic β cell interleukin-22 receptor subunit alpha 1 deficiency impairs β cell function in type 2 diabetes via cytochrome b5 reductase 3.
    Article Snippet: .. Antigen retrieval was carried out by boiling in Tris-EDTA buffer or citrate buffer for microwaving 10 min. After cooling to room temperature, sections were covered in blocking buffer (5% donkey serum in PBS) for 1 h. Primary antibodies were applied at a dilution of 1:400 for INSULIN (Cell Signaling Technology, 8138), 1:400 for GLUCAGON (Cell Signaling Technology, 2760), 1:50 for IL22RA1 (R&D SYSTEM, 496514), 1:100 for CYB5R3 (Proteintech, 10894-1-AP), 1:100 for MAFA (Cell Signaling Technology, 79737), 1:100 for PDX1 (Abcam, ab47308), 1:100 for NKX6.1 (Cell Signaling Technology, 54551), and 1:400 for GFP (Abcam, ab13970) overnight at 4 C. Next day, sections were washed in PBS for three times and incubated with Alexa Fluor conjugated secondary antibodies (Abcam, ab150106; Abcam, ab150073; Invitrogen, A21208) at a dilution of 1:400 for 1 h. Nuclei were counterstained with DAPI (Beyotime, C1002) at a dilution of 1:5000 for 5 min. .. Images were acquired using a Leica microscope (Leica, DM4B) and scanned by AKOYA Vectra Polaris.

    Western Blot:

    Article Title: Obesity-induced upregulation of miR-483-5p impairs the function and identity of pancreatic β-cells.
    Article Snippet: Funding information National Natural Science Foundation of China, Grant/Award Numbers: 32171116, 32371168, 82370803, 82170810; Research Project of Taizhou Clinical Medical College of Nanjing Medical University, Grant/Award Number: TZKY20230310 Abstract Aim: To assess the expression and function of miR-483-5p in diabetic β cells.. Methods: The expression of miR-483-5p was evaluated in the pancreatic islets of obesity mouse models by quantitative reverse transcription polymerase chain reaction.. Dual-luciferase activity, and western blotting assays, were utilized for miR483-5p target gene verification.

    Article Title: GLP-1 receptor agonist protects glucose-stimulated insulin secretion in pancreatic β-cells against lipotoxicity via PPARδ/UCP2 pathway
    Article Snippet: .. The antibodies used in WB were: INSULIN (1:1000, ab181547, Abcam), PPARδ (1:1000, 74076 S, CST), UCP2 (1:1000, 89326 S, CST), PDX1 (1:1000, ab219207, Abcam), MAFA (1:1000, 7937 S, CST), IRS1 (1:1000, 2390 S, CST), GCK (1:1000, 19666-1-AP, Proteintech), β-ACTIN (1:1000, PM053, MBL) and β-TUBULIN (1:1000, 2128 S, CST). .. For quantification, target protein band intensities were normalised against β-TUBULIN and analysed by densitometry using ImageJ software.

    Article Title: Huanglian-Renshen-Decoction Maintains Islet β-Cell Identity in T2DM Mice through Regulating GLP-1 and GLP-1R in Both Islet and Intestine.
    Article Snippet: Type 2 diabetes mellitus (T2DM) is a metabolic disease that severely threatens human health and general well-being.. According to a survey by the International Diabetes Federation, 400 million patients are diagnosed with T2DM yearly, of whom 9 million are critically ill. T2DM results from insulin resistance and β-cell dysfunction, gradually leading to uncontrollable hyperglycemia.. According to the latest research, islet β-cell identity loss is one of the mechanisms of T2DM, contributing to insufficient insulin secretion; islet β-cells transdifferentiate into other cells without insulin secretion function.



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    a Scheme for the generation of an inducible β-cell-specific TBL1X and TBL1XR1 knockout. b Random fed blood glucose levels over time in iTBL/RβKO ( n = 9) and control ( n = 9) mice on HFD. c Total pancreas insulin content normalized to protein levels in iTBL/RβKO and control mice 4 and 11 weeks after tamoxifen administration. n = 3 for 4w control and iTBL/RβKO mice, n = 6 for 11w control mice, n = 4 for 11w iTBL/RβKO mice. d , e Blood glucose ( d ) and plasma insulin ( e ) levels during an oral glucose tolerance test after 22 weeks of HFD. Corresponding area under the curve in iTBL/RβKO ( n = 8) and control ( n = 9) mice ( d , right). f , g Relative mRNA expression determined by qPCR in pancreatic islets of iTBL/RβKO and control mice of Tbl1x and Tbl1xr1 ( f ) and islet genes ( g ). Control mice Tbl1x , Tbl1xr1 , Ins1 , Ins2 , Nkx6.1 , Slc2a2 , <t>Mafa</t> , Pdx1 , Pax6 , Ucn3 : n = 9, control mice ChgA , Ngn3 , Ldha , Hk1 : n = 8, iTBL/RβKO mice Tbl1x , Ngn3 , Ldha , Hk1 : n = 7, iTBL/RβKO mice Tbl1xr1 , Ins1 , Ins2 , Slc2a2 , Mafa n = 6, iTBL/RβKO mice Nkx6.1 , Pdx1 , Pax6 , Ucn3 , ChgA : n = 5. h α/β-cell mass ratio of pancreatic islets from iTBL/RβKO ( n = 4) and control mice ( n = 4) on HFD, 24 weeks after knockout induction. i Representative immunofluorescent staining of insulin + (blue, β-cells) and glucagon + (red, α-cells) cells of paraffin-embedded pancreas from iTBL/RβKO and control mice on HFD, 24 weeks after knockout induction. Each point represents one mouse. Data are represented as mean ± SEM. The following statistical tests were applied: two-sided student’s t test ( d – Area under the curve, f – h ) and 2-way ANOVA with Šidák’s multiple comparison post hoc test ( b – d – time course, e ). Source data are provided as a Source Data file.
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    a Scheme for the generation of an inducible β-cell-specific TBL1X and TBL1XR1 knockout. b Random fed blood glucose levels over time in iTBL/RβKO ( n = 9) and control ( n = 9) mice on HFD. c Total pancreas insulin content normalized to protein levels in iTBL/RβKO and control mice 4 and 11 weeks after tamoxifen administration. n = 3 for 4w control and iTBL/RβKO mice, n = 6 for 11w control mice, n = 4 for 11w iTBL/RβKO mice. d , e Blood glucose ( d ) and plasma insulin ( e ) levels during an oral glucose tolerance test after 22 weeks of HFD. Corresponding area under the curve in iTBL/RβKO ( n = 8) and control ( n = 9) mice ( d , right). f , g Relative mRNA expression determined by qPCR in pancreatic islets of iTBL/RβKO and control mice of Tbl1x and Tbl1xr1 ( f ) and islet genes ( g ). Control mice Tbl1x , Tbl1xr1 , Ins1 , Ins2 , Nkx6.1 , Slc2a2 , <t>Mafa</t> , Pdx1 , Pax6 , Ucn3 : n = 9, control mice ChgA , Ngn3 , Ldha , Hk1 : n = 8, iTBL/RβKO mice Tbl1x , Ngn3 , Ldha , Hk1 : n = 7, iTBL/RβKO mice Tbl1xr1 , Ins1 , Ins2 , Slc2a2 , Mafa n = 6, iTBL/RβKO mice Nkx6.1 , Pdx1 , Pax6 , Ucn3 , ChgA : n = 5. h α/β-cell mass ratio of pancreatic islets from iTBL/RβKO ( n = 4) and control mice ( n = 4) on HFD, 24 weeks after knockout induction. i Representative immunofluorescent staining of insulin + (blue, β-cells) and glucagon + (red, α-cells) cells of paraffin-embedded pancreas from iTBL/RβKO and control mice on HFD, 24 weeks after knockout induction. Each point represents one mouse. Data are represented as mean ± SEM. The following statistical tests were applied: two-sided student’s t test ( d – Area under the curve, f – h ) and 2-way ANOVA with Šidák’s multiple comparison post hoc test ( b – d – time course, e ). Source data are provided as a Source Data file.
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    a Scheme for the generation of an inducible β-cell-specific TBL1X and TBL1XR1 knockout. b Random fed blood glucose levels over time in iTBL/RβKO ( n = 9) and control ( n = 9) mice on HFD. c Total pancreas insulin content normalized to protein levels in iTBL/RβKO and control mice 4 and 11 weeks after tamoxifen administration. n = 3 for 4w control and iTBL/RβKO mice, n = 6 for 11w control mice, n = 4 for 11w iTBL/RβKO mice. d , e Blood glucose ( d ) and plasma insulin ( e ) levels during an oral glucose tolerance test after 22 weeks of HFD. Corresponding area under the curve in iTBL/RβKO ( n = 8) and control ( n = 9) mice ( d , right). f , g Relative mRNA expression determined by qPCR in pancreatic islets of iTBL/RβKO and control mice of Tbl1x and Tbl1xr1 ( f ) and islet genes ( g ). Control mice Tbl1x , Tbl1xr1 , Ins1 , Ins2 , Nkx6.1 , Slc2a2 , <t>Mafa</t> , Pdx1 , Pax6 , Ucn3 : n = 9, control mice ChgA , Ngn3 , Ldha , Hk1 : n = 8, iTBL/RβKO mice Tbl1x , Ngn3 , Ldha , Hk1 : n = 7, iTBL/RβKO mice Tbl1xr1 , Ins1 , Ins2 , Slc2a2 , Mafa n = 6, iTBL/RβKO mice Nkx6.1 , Pdx1 , Pax6 , Ucn3 , ChgA : n = 5. h α/β-cell mass ratio of pancreatic islets from iTBL/RβKO ( n = 4) and control mice ( n = 4) on HFD, 24 weeks after knockout induction. i Representative immunofluorescent staining of insulin + (blue, β-cells) and glucagon + (red, α-cells) cells of paraffin-embedded pancreas from iTBL/RβKO and control mice on HFD, 24 weeks after knockout induction. Each point represents one mouse. Data are represented as mean ± SEM. The following statistical tests were applied: two-sided student’s t test ( d – Area under the curve, f – h ) and 2-way ANOVA with Šidák’s multiple comparison post hoc test ( b – d – time course, e ). Source data are provided as a Source Data file.
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    a Scheme for the generation of an inducible β-cell-specific TBL1X and TBL1XR1 knockout. b Random fed blood glucose levels over time in iTBL/RβKO ( n = 9) and control ( n = 9) mice on HFD. c Total pancreas insulin content normalized to protein levels in iTBL/RβKO and control mice 4 and 11 weeks after tamoxifen administration. n = 3 for 4w control and iTBL/RβKO mice, n = 6 for 11w control mice, n = 4 for 11w iTBL/RβKO mice. d , e Blood glucose ( d ) and plasma insulin ( e ) levels during an oral glucose tolerance test after 22 weeks of HFD. Corresponding area under the curve in iTBL/RβKO ( n = 8) and control ( n = 9) mice ( d , right). f , g Relative mRNA expression determined by qPCR in pancreatic islets of iTBL/RβKO and control mice of Tbl1x and Tbl1xr1 ( f ) and islet genes ( g ). Control mice Tbl1x , Tbl1xr1 , Ins1 , Ins2 , Nkx6.1 , Slc2a2 , Mafa , Pdx1 , Pax6 , Ucn3 : n = 9, control mice ChgA , Ngn3 , Ldha , Hk1 : n = 8, iTBL/RβKO mice Tbl1x , Ngn3 , Ldha , Hk1 : n = 7, iTBL/RβKO mice Tbl1xr1 , Ins1 , Ins2 , Slc2a2 , Mafa n = 6, iTBL/RβKO mice Nkx6.1 , Pdx1 , Pax6 , Ucn3 , ChgA : n = 5. h α/β-cell mass ratio of pancreatic islets from iTBL/RβKO ( n = 4) and control mice ( n = 4) on HFD, 24 weeks after knockout induction. i Representative immunofluorescent staining of insulin + (blue, β-cells) and glucagon + (red, α-cells) cells of paraffin-embedded pancreas from iTBL/RβKO and control mice on HFD, 24 weeks after knockout induction. Each point represents one mouse. Data are represented as mean ± SEM. The following statistical tests were applied: two-sided student’s t test ( d – Area under the curve, f – h ) and 2-way ANOVA with Šidák’s multiple comparison post hoc test ( b – d – time course, e ). Source data are provided as a Source Data file.

    Journal: Nature Communications

    Article Title: TBL1X/TBL1XR1 govern β-cell identity through a PAX6-containing gene regulatory network

    doi: 10.1038/s41467-026-72077-5

    Figure Lengend Snippet: a Scheme for the generation of an inducible β-cell-specific TBL1X and TBL1XR1 knockout. b Random fed blood glucose levels over time in iTBL/RβKO ( n = 9) and control ( n = 9) mice on HFD. c Total pancreas insulin content normalized to protein levels in iTBL/RβKO and control mice 4 and 11 weeks after tamoxifen administration. n = 3 for 4w control and iTBL/RβKO mice, n = 6 for 11w control mice, n = 4 for 11w iTBL/RβKO mice. d , e Blood glucose ( d ) and plasma insulin ( e ) levels during an oral glucose tolerance test after 22 weeks of HFD. Corresponding area under the curve in iTBL/RβKO ( n = 8) and control ( n = 9) mice ( d , right). f , g Relative mRNA expression determined by qPCR in pancreatic islets of iTBL/RβKO and control mice of Tbl1x and Tbl1xr1 ( f ) and islet genes ( g ). Control mice Tbl1x , Tbl1xr1 , Ins1 , Ins2 , Nkx6.1 , Slc2a2 , Mafa , Pdx1 , Pax6 , Ucn3 : n = 9, control mice ChgA , Ngn3 , Ldha , Hk1 : n = 8, iTBL/RβKO mice Tbl1x , Ngn3 , Ldha , Hk1 : n = 7, iTBL/RβKO mice Tbl1xr1 , Ins1 , Ins2 , Slc2a2 , Mafa n = 6, iTBL/RβKO mice Nkx6.1 , Pdx1 , Pax6 , Ucn3 , ChgA : n = 5. h α/β-cell mass ratio of pancreatic islets from iTBL/RβKO ( n = 4) and control mice ( n = 4) on HFD, 24 weeks after knockout induction. i Representative immunofluorescent staining of insulin + (blue, β-cells) and glucagon + (red, α-cells) cells of paraffin-embedded pancreas from iTBL/RβKO and control mice on HFD, 24 weeks after knockout induction. Each point represents one mouse. Data are represented as mean ± SEM. The following statistical tests were applied: two-sided student’s t test ( d – Area under the curve, f – h ) and 2-way ANOVA with Šidák’s multiple comparison post hoc test ( b – d – time course, e ). Source data are provided as a Source Data file.

    Article Snippet: The following TaqMan probes were used: Tbp - Mm01277042_m1, Tbl1x - Mm01222202_m1, Tbl1xr1 - Mm01283877_m1, Ins1 - Mm01259683_g1, Ins2 - Mm00731595_gH, Nkx6.1 - Mm00454961_m1, Slc2a2 - Mm00454961_m1, Mafa - Mm00845206_s1, Pdx1 - Mm00435565_m1, Pax6 - Mm00443081_m1, Ucn3 - Mm00453206_s1, ChgA - Mm00514341_m1, Ngn3 - Mm00437606_s1, Ldha - Mm01612132_g1, Hk1 - Mm00439344_m1, TBP - Hs00427620_m1, TBL1X - Hs00959540_m1, TBL1XR1 - Hs00226564_m1.

    Techniques: Knock-Out, Control, Clinical Proteomics, Expressing, Staining, Comparison