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nbp2 44607  (Novus Biologicals)


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    Structured Review

    Novus Biologicals nbp2 44607
    Nbp2 44607, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 8 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nbp2+44607/WT1+Antibody+(WT1%2F857+%2B+6F-H2)/pmc11814332__41467_2025_56891_MOESM1_ESM-118-247-245
    Average 93 stars, based on 8 article reviews
    nbp2 44607 - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Incubation:

    Article Title: Fibroblast growth factor 1 ameliorates diabetic nephropathy by an anti-inflammatory mechanism
    Article Snippet: .. Slides were blocked using 5% bovine serum albumin for 30 minutes and then incubated overnight at 4 °C with both FGF1 antibody (Abcam, ab207321, 1:200) and an antibody of a specific marker (anti-smooth muscle actin, Abcam, ab7817, 1:200; anti-Wilms tumor 1 [Novus Biologicals, Littleton, CO], NBP2-44607, 1:200); and anti-aquaporin 1 [Santa Cruz Biotechnology, Inc., Dallas, TX, sc-32737, 1:200; anti-CD68 from Abcam, ab955, 1:200), respectively. .. Slides were then correspondingly incubated with 2 kinds of secondary antibody (TRITC-labeled antibody from Abcam, ab6786, 1:500; Alexa Fluor–labeled antibody from Abcam, ab150075, 1:500) at 37 °C for 1 hour, and washed by PBS for 4 times.

    Marker:

    Article Title: Fibroblast growth factor 1 ameliorates diabetic nephropathy by an anti-inflammatory mechanism
    Article Snippet: .. Slides were blocked using 5% bovine serum albumin for 30 minutes and then incubated overnight at 4 °C with both FGF1 antibody (Abcam, ab207321, 1:200) and an antibody of a specific marker (anti-smooth muscle actin, Abcam, ab7817, 1:200; anti-Wilms tumor 1 [Novus Biologicals, Littleton, CO], NBP2-44607, 1:200); and anti-aquaporin 1 [Santa Cruz Biotechnology, Inc., Dallas, TX, sc-32737, 1:200; anti-CD68 from Abcam, ab955, 1:200), respectively. .. Slides were then correspondingly incubated with 2 kinds of secondary antibody (TRITC-labeled antibody from Abcam, ab6786, 1:500; Alexa Fluor–labeled antibody from Abcam, ab150075, 1:500) at 37 °C for 1 hour, and washed by PBS for 4 times.

    other:

    Article Title: CerS6 links ceramide metabolism to innate immune responses in diabetic kidney disease
    Article Snippet: Antibody Source Catalog number Application Rabbit anti- CerS6 Gentex Cat# GTX17028 dilution 1:1000 for WB (mouse kidney tissue) Rabbit anti- CerS6 Novus Cat#76965 dilution 1:500 for IHC (mouse kidney section), 1:500 for IF (mouse kidney section) Rabbit anti- CerS6 Sigma Cat# HPA063527 dilution 1:1000 for IF (human kidney section), 1:1000 for WB (HPC) Rabbit anti- STING CST Cat# 13647S dilution 1:1000 for WB, 1:200 for IF Rabbit anti- cGAS CST Cat# 15102T dilution 1:1000 for WB (HPC) Rabbit anti- cGAS Proteintech Cat#68640-1-Ig dilution 1:2000 for WB (mouse kidney tissue), 1:500 for IF (mouse kidney section) Rabbit anti- cGAS Abcam Cat# ab302617 dilution 1:50 for IF (HPC coverslip) Rabbit anti-p- TBK1 CST Cat# 5483S dilution 1:1000 for WB Rabbit anti- TBK1 Abcam Cat# ab40676 dilution 1:5000 for WB Rabbit anti-p- NF-κB (p-p65) CST Cat# 3033S dilution 1:1000 for WB Rabbit anti-NF- κB (p65) Santa Cruz Cat# sc-8008 dilution 1:500 for WB Rabbit anti- VDAC1 Abcam Cat# ab306581 dilution 1:1000 for WB, 1:1000 Mouse anti- BAX Proteintech Cat# 60267-1-Ig dilution 1:10000 for WB Mouse anti- dsDNA Abcam Cat# ab27156 dilution 1:500 for IF Mouse anti- Tomm20 Novus Cat# H00009804 dilution 1:200 for IF Rabbit anti- CD68 Abcam Cat# ab303565 dilution 1:100 for IF Rabbit anti- Nephrin Novus Cat# NBP1-30130 dilution 1:200 for IF Rabbit anti- Nephrin Proteintech Cat# 22912-1-AP dilution 1:2000 for WB Mouse anti- Synaptopodin Progen Cat# 65194 dilution 1:100 for IF Mouse anti- Synaptopodin Santa Cruz Cat# sc-515842 dilution 1:500 for WB Mouse anti-WT- 1 Novus Cat# NBP2-44607 dilution 1:200 for IF Rabbit anti-WT- 1 BOSTER Cat# BM4216 dilution 1:1000 for WB Mouse anti-α- tubulin Proteintech Cat# 66031-1-Ig dilution 1:20000 for WB Mouse anti-β- actin Proteintech Cat# 66009-1-Ig dilution 1:20000 for WB Mouse anti- GAPDH Proteintech Cat# 60004-1-Ig dilution 1:50000 for WB



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    Fig. 2. Diosgenin regulated SIRT6 and reduced lipid accumulation in glomerulus. (A,B) SIRT6 stained by immunohistochemistry, scale bar, 25 μm (A) and mean optic intensity quantified by Image Pro Plus (B, n = 6 for each group); (C,D) Double labeling of immunofluorescence about SIRT6 and <t>WT1</t> (marker of podocyte) by confocal, scale bar, 50 μm (C) and mean fluorescence intensity quantified by Image Pro Plus(D, n = 6 for each group); (E) Lipid metabolism factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (F) Inflammation factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (G-I) Frozen section of kidney stained with Oil red and ADRP was stained by immunohistochemistry, scale bar, 25 μm (G), Oil red quantification by Image Pro Plus (H, n = 6 for each group) and ADRP quantified by Image Pro Plus (I, n = 6 for each group).
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    Novus Biologicals wilms tumor 1 antibody
    Fig. 2. Diosgenin regulated SIRT6 and reduced lipid accumulation in glomerulus. (A,B) SIRT6 stained by immunohistochemistry, scale bar, 25 μm (A) and mean optic intensity quantified by Image Pro Plus (B, n = 6 for each group); (C,D) Double labeling of immunofluorescence about SIRT6 and <t>WT1</t> (marker of podocyte) by confocal, scale bar, 50 μm (C) and mean fluorescence intensity quantified by Image Pro Plus(D, n = 6 for each group); (E) Lipid metabolism factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (F) Inflammation factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (G-I) Frozen section of kidney stained with Oil red and ADRP was stained by immunohistochemistry, scale bar, 25 μm (G), Oil red quantification by Image Pro Plus (H, n = 6 for each group) and ADRP quantified by Image Pro Plus (I, n = 6 for each group).
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    Antibodies and assay kits

    Journal: Kidney360

    Article Title: AMPK-SP1–Guided Dynein Expression Represents a New Energy-Responsive Mechanism and Therapeutic Target for Diabetic Nephropathy

    doi: 10.34067/KID.0000000000000392

    Figure Lengend Snippet: Antibodies and assay kits

    Article Snippet: Mouse anti-WT1 , Novus Biologicals , NBP2-44607.

    Techniques:

    Fig. 2. Diosgenin regulated SIRT6 and reduced lipid accumulation in glomerulus. (A,B) SIRT6 stained by immunohistochemistry, scale bar, 25 μm (A) and mean optic intensity quantified by Image Pro Plus (B, n = 6 for each group); (C,D) Double labeling of immunofluorescence about SIRT6 and WT1 (marker of podocyte) by confocal, scale bar, 50 μm (C) and mean fluorescence intensity quantified by Image Pro Plus(D, n = 6 for each group); (E) Lipid metabolism factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (F) Inflammation factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (G-I) Frozen section of kidney stained with Oil red and ADRP was stained by immunohistochemistry, scale bar, 25 μm (G), Oil red quantification by Image Pro Plus (H, n = 6 for each group) and ADRP quantified by Image Pro Plus (I, n = 6 for each group).

    Journal: Phytomedicine : international journal of phytotherapy and phytopharmacology

    Article Title: Diosgenin protects against podocyte injury in early phase of diabetic nephropathy through regulating SIRT6.

    doi: 10.1016/j.phymed.2022.154276

    Figure Lengend Snippet: Fig. 2. Diosgenin regulated SIRT6 and reduced lipid accumulation in glomerulus. (A,B) SIRT6 stained by immunohistochemistry, scale bar, 25 μm (A) and mean optic intensity quantified by Image Pro Plus (B, n = 6 for each group); (C,D) Double labeling of immunofluorescence about SIRT6 and WT1 (marker of podocyte) by confocal, scale bar, 50 μm (C) and mean fluorescence intensity quantified by Image Pro Plus(D, n = 6 for each group); (E) Lipid metabolism factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (F) Inflammation factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (G-I) Frozen section of kidney stained with Oil red and ADRP was stained by immunohistochemistry, scale bar, 25 μm (G), Oil red quantification by Image Pro Plus (H, n = 6 for each group) and ADRP quantified by Image Pro Plus (I, n = 6 for each group).

    Article Snippet: The primary antibody includes SIRT6 (ab191385, abcam), WT1 (NBP2-44607,NOVUS), NEPHRIN Z. Wang et al. Phytomedicine 104 (2022) 154276 (ab216341, abcam), PODOCIN (ab181143, abcam), DESMIN (A3736, ABclonal).

    Techniques: Staining, Immunohistochemistry, Labeling, Immunofluorescence, Marker, Fluorescence, Quantitative RT-PCR

    Fig. 4. The effect of diosgenin in the regulation of SIRT6 and reduction of lipid accumulation in glomerulus was blocked by by OSS_128167 and MDL800 had the same effect as diosgenin. (A,B) SIRT6 stained by immunohistochemistry, scale bar, 25 μm (A) and mean optic intensity quantified by Image Pro Plus(B, n = 6 for each group); (C,D) Double labeling of immunofluorescence about SIRT6 and WT1 (marker of podocyte) by confocal, scale bar, 50 μm (C) and mean fluorescence intensity quantified by Image Pro Plus (D, n = 6 for each group); (E) Inflammation factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (F) Lipid metabolism factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (G-I) Frozen section of kidney stained with Oil red and ADRP was stained by immunohistochemistry, scale bar, 25 μm (G), Oil red quantification by Image Pro Plus (H, n = 6 for each group) and ADRP quantified by Image Pro Plus (I, n = 6 for each group).

    Journal: Phytomedicine : international journal of phytotherapy and phytopharmacology

    Article Title: Diosgenin protects against podocyte injury in early phase of diabetic nephropathy through regulating SIRT6.

    doi: 10.1016/j.phymed.2022.154276

    Figure Lengend Snippet: Fig. 4. The effect of diosgenin in the regulation of SIRT6 and reduction of lipid accumulation in glomerulus was blocked by by OSS_128167 and MDL800 had the same effect as diosgenin. (A,B) SIRT6 stained by immunohistochemistry, scale bar, 25 μm (A) and mean optic intensity quantified by Image Pro Plus(B, n = 6 for each group); (C,D) Double labeling of immunofluorescence about SIRT6 and WT1 (marker of podocyte) by confocal, scale bar, 50 μm (C) and mean fluorescence intensity quantified by Image Pro Plus (D, n = 6 for each group); (E) Inflammation factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (F) Lipid metabolism factors in glomerulus were measured by RT-qPCR, n = 6 for each group; (G-I) Frozen section of kidney stained with Oil red and ADRP was stained by immunohistochemistry, scale bar, 25 μm (G), Oil red quantification by Image Pro Plus (H, n = 6 for each group) and ADRP quantified by Image Pro Plus (I, n = 6 for each group).

    Article Snippet: The primary antibody includes SIRT6 (ab191385, abcam), WT1 (NBP2-44607,NOVUS), NEPHRIN Z. Wang et al. Phytomedicine 104 (2022) 154276 (ab216341, abcam), PODOCIN (ab181143, abcam), DESMIN (A3736, ABclonal).

    Techniques: Staining, Immunohistochemistry, Labeling, Immunofluorescence, Marker, Fluorescence, Quantitative RT-PCR

    Fig. 5. Diosgenin protected against MPC5 injury by regulating SIRT6. (A-E) Protein including NEPHRIN and PODOCIN measured by western blot (A) and DESMIN was measured by immunofluorescence, scale bar, 50 μm (B) and NEPHRIN quantification (C, n = 6 for each group), PODOCIN quantification (D,n = 6 for each group) and DESMIN quantification (E,n = 6 for each group) by Image Pro Plus; (F-J) Protein including NEPHRIN and PODOCIN measured by western blot (F) and DESMIN was measured by immunofluorescence, scale bar, 50 μm (G) and NEPHRIN quantification (H, n = 6 for each group),PODOCIN quantification (I, n = 6 for each group) and DESMIN quantification (J, n = 6 for each group) by Image Pro Plus; (K and L) Double labeling of immunofluorescence about SIRT6 and WT1 by confocal,scale bar, 50 μm (K) and SIRT6 quantification by Image Pro Plus (L, n = 6 for each group).

    Journal: Phytomedicine : international journal of phytotherapy and phytopharmacology

    Article Title: Diosgenin protects against podocyte injury in early phase of diabetic nephropathy through regulating SIRT6.

    doi: 10.1016/j.phymed.2022.154276

    Figure Lengend Snippet: Fig. 5. Diosgenin protected against MPC5 injury by regulating SIRT6. (A-E) Protein including NEPHRIN and PODOCIN measured by western blot (A) and DESMIN was measured by immunofluorescence, scale bar, 50 μm (B) and NEPHRIN quantification (C, n = 6 for each group), PODOCIN quantification (D,n = 6 for each group) and DESMIN quantification (E,n = 6 for each group) by Image Pro Plus; (F-J) Protein including NEPHRIN and PODOCIN measured by western blot (F) and DESMIN was measured by immunofluorescence, scale bar, 50 μm (G) and NEPHRIN quantification (H, n = 6 for each group),PODOCIN quantification (I, n = 6 for each group) and DESMIN quantification (J, n = 6 for each group) by Image Pro Plus; (K and L) Double labeling of immunofluorescence about SIRT6 and WT1 by confocal,scale bar, 50 μm (K) and SIRT6 quantification by Image Pro Plus (L, n = 6 for each group).

    Article Snippet: The primary antibody includes SIRT6 (ab191385, abcam), WT1 (NBP2-44607,NOVUS), NEPHRIN Z. Wang et al. Phytomedicine 104 (2022) 154276 (ab216341, abcam), PODOCIN (ab181143, abcam), DESMIN (A3736, ABclonal).

    Techniques: Western Blot, Immunofluorescence, Labeling