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rabbit monoclonal anti mafa d2z6n  (Cell Signaling Technology Inc)


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    Structured Review

    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, 2026-11
    95/100 stars

    Images

    Related Articles

    Cell-Signaling:

    Article Title: Stimulation to secrete insulin induces pancreatic β-cell dysfunction through Tfe3 activation
    Article Snippet: .. Rabbit monoclonal anti-MAFA (D2Z6N) , Cell Signaling Technology , Cat# 79737; RRID: AB_2799938. .. Rabbit polyclonal anti-PDX1 , Millipore , Cat# 05–718; RRID: AB_417404.

    Article Title: PDX1 phosphorylation at S61 by mTORC1 links nutrient signaling to β cell function and metabolic disease
    Article Snippet: Mouse monoclonal anti-KLF11 , Sigma-Aldrich , #SAB1404583; RRID: AB_10740381. .. Rabbit monoclonal anti-MAFA , Cell signaling Technology , #79737; RRID: AB_2799938. .. Rabbit polyclonal anti-GLUT2 , Abcam , #ab54460; RRID: AB_880234.

    other:

    Article Title: The RNA-binding protein CPEB1 marks healthy adult β cells in mice but is dispensable for β cell identity and function
    Article Snippet: The following primary antibodies were guinea pig anti-insulin 1:6 (Agilent, IR002), rabbit anti-glucagon 1:200 (Cell Signaling Technology, 2760 S), mouse anti-glucagon (Sigma, G2654), rabbit anti-UCN3 1:500 (Phoenix Pharmaceuticals, H-019-29), rabbit anti-MAFA 1:200 (Cell Signaling Technology, 79737 S), rabbit anti-somatostatin 1:500 (Phoenix Pharmaceuticals, G-060-03), rabbit anti-Ki67 1:400 (Cell Signaling Technology, 9129 S), and rat anti-CD45 1:10 (BD Biosciences, 550539).

    Article Title: The RNA-binding protein CPEB1 marks healthy adult β cells in mice but is dispensable for β cell identity and function.
    Article Snippet: The following primary antibodies were guinea pig anti-insulin 1:6 (Agilent, IR002), rabbit anti-glucagon 1:200 (Cell Signaling Technology, 2760S), mouse anti-glucagon (Sigma, G2654), rabbit anti-UCN3 1:500 (Phoenix Pharmaceuticals, H-019-29), rabbit anti-MAFA 1:200 (Cell Signaling Technology, 79737S), rabbit anti-somatostatin 1:500 (Phoenix Pharmaceuticals, G-060-03), rabbit anti-Ki67 1:400 (Cell Signaling Technology, 9129S), and rat anti-CD45 1:10 (BD Biosciences, 550539).

    Western Blot:

    Article Title: Genetic background influences the phenotypic penetrance by MAFA S64F MODY in male mice
    Article Snippet: .. MAFA protein levels were normalized to endogenous β-actin by immunoblotting with anti-MAFA (Cell Signaling Technology, 79737) and anti–β-actin (MilliporeSigma, MAB1501) antibodies. .. Horseradish peroxidase–conjugated anti-rabbit (31460, Thermo Fisher Scientific) or anti-goat (31402, Thermo Fisher Scientific) secondary antibodies were used at 1:5000.

    Immunoprecipitation:

    Article Title: A 3′ UTR polymorphism g.1618 G > A in the MAFA gene modulates miR-3678-3p binding and enhances meat production in sheep via the MAFA/GHR/JAK2 pathway
    Article Snippet: .. Immunoprecipitation was performed using an anti-MAFA antibody (#79,737, Cell Signaling Technology, USA), and IgG served as a negative control. ..

    Negative Control:

    Article Title: A 3′ UTR polymorphism g.1618 G > A in the MAFA gene modulates miR-3678-3p binding and enhances meat production in sheep via the MAFA/GHR/JAK2 pathway
    Article Snippet: .. Immunoprecipitation was performed using an anti-MAFA antibody (#79,737, Cell Signaling Technology, USA), and IgG served as a negative control. ..

    Blocking Assay:

    Article Title: Presenilin-1 controls glucose metabolism and identity of pancreatic beta cells
    Article Snippet: For blocking, the pancreatic tissue slices were incubated with blocking buffer (PBS containing 5% BSA (A2153, Sigma Aldrich)) supplemented with 0.1% Triton X-100 (37240, Serva Electrophoresis GmbH) for 1 hour at room temperature. .. After removal of the blocking solution, primary antibody was diluted in blocking buffer and added in the following concentrations: guinea-pig anti-insulin (ab7842, abcam, 1:100), rabbit anti-glucagon (A14609, ABclonal, 1:100), mouse anti-neurogenin (sc-374442, Santa Cruz Biotechnology 1:200), rabbit anti-PDX1 (5679S, Cell Signaling, 1:200), rabbit anti-MAFA (79737S, Cell Signaling, 1:500), rabbit anti-NKX6.1 (Cell Signaling, 54551S, 1:400). ..



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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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    Image Search Results


    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