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anti cellular myelocytomatosis oncogene c myc  (ABclonal Biotechnology)
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ABclonal Biotechnology anti cellular myelocytomatosis oncogene c myc
SPARC knockdown disrupts Wnt signaling and β-catenin nuclear translocation. ( A , B ) Western blot and RT-qPCR analysis showing reduced β-catenin <t>and</t> <t>c-Myc</t> protein and mRNA expression in HCECs following SPARC knockdown ( n = 5 independent experiments per group). ( C , D ) Western blot and RT-qPCR analysis of β-catenin protein and mRNA expression in corneal epithelial cells from WT and Sparc −/− mice at the indicated postinjury time points ( n = 3 independent pooled biological replicates per group). ( E , F ) Immunofluorescence staining of β-catenin ( red ) and DAPI ( blue ) in HCECs after SPARC knockdown ( n = 5 independent experiments per group). ( G ) Immunofluorescence images and quantification of β-catenin ( green ) in corneal sections from WT and Sparc −/− mice at different postinjury time points; nuclei were counterstained with DAPI ( blue ) ( n = 5 mice per group). ( H , I ) Scratch-wound assay and quantification of wound closure in HCECs after β-catenin knockdown with or without exogenous SPARC supplementation (the knockdown efficiency of β-catenin in HCECs is shown in B; n = 5 independent experiments per group). Scale bars are indicated in the images. Data are presented as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001.
Anti Cellular Myelocytomatosis Oncogene C Myc, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti c myc  (ABclonal Biotechnology)
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ABclonal Biotechnology anti c myc
SPARC knockdown disrupts Wnt signaling and β-catenin nuclear translocation. ( A , B ) Western blot and RT-qPCR analysis showing reduced β-catenin <t>and</t> <t>c-Myc</t> protein and mRNA expression in HCECs following SPARC knockdown ( n = 5 independent experiments per group). ( C , D ) Western blot and RT-qPCR analysis of β-catenin protein and mRNA expression in corneal epithelial cells from WT and Sparc −/− mice at the indicated postinjury time points ( n = 3 independent pooled biological replicates per group). ( E , F ) Immunofluorescence staining of β-catenin ( red ) and DAPI ( blue ) in HCECs after SPARC knockdown ( n = 5 independent experiments per group). ( G ) Immunofluorescence images and quantification of β-catenin ( green ) in corneal sections from WT and Sparc −/− mice at different postinjury time points; nuclei were counterstained with DAPI ( blue ) ( n = 5 mice per group). ( H , I ) Scratch-wound assay and quantification of wound closure in HCECs after β-catenin knockdown with or without exogenous SPARC supplementation (the knockdown efficiency of β-catenin in HCECs is shown in B; n = 5 independent experiments per group). Scale bars are indicated in the images. Data are presented as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001.
Anti C Myc, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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ae009  (ABclonal Biotechnology)
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SPARC knockdown disrupts Wnt signaling and β-catenin nuclear translocation. ( A , B ) Western blot and RT-qPCR analysis showing reduced β-catenin <t>and</t> <t>c-Myc</t> protein and mRNA expression in HCECs following SPARC knockdown ( n = 5 independent experiments per group). ( C , D ) Western blot and RT-qPCR analysis of β-catenin protein and mRNA expression in corneal epithelial cells from WT and Sparc −/− mice at the indicated postinjury time points ( n = 3 independent pooled biological replicates per group). ( E , F ) Immunofluorescence staining of β-catenin ( red ) and DAPI ( blue ) in HCECs after SPARC knockdown ( n = 5 independent experiments per group). ( G ) Immunofluorescence images and quantification of β-catenin ( green ) in corneal sections from WT and Sparc −/− mice at different postinjury time points; nuclei were counterstained with DAPI ( blue ) ( n = 5 mice per group). ( H , I ) Scratch-wound assay and quantification of wound closure in HCECs after β-catenin knockdown with or without exogenous SPARC supplementation (the knockdown efficiency of β-catenin in HCECs is shown in B; n = 5 independent experiments per group). Scale bars are indicated in the images. Data are presented as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001.
Ae009, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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resource source identifier anti-gfp abclonal cat#ae011  (ABclonal Biotechnology)
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SPARC knockdown disrupts Wnt signaling and β-catenin nuclear translocation. ( A , B ) Western blot and RT-qPCR analysis showing reduced β-catenin <t>and</t> <t>c-Myc</t> protein and mRNA expression in HCECs following SPARC knockdown ( n = 5 independent experiments per group). ( C , D ) Western blot and RT-qPCR analysis of β-catenin protein and mRNA expression in corneal epithelial cells from WT and Sparc −/− mice at the indicated postinjury time points ( n = 3 independent pooled biological replicates per group). ( E , F ) Immunofluorescence staining of β-catenin ( red ) and DAPI ( blue ) in HCECs after SPARC knockdown ( n = 5 independent experiments per group). ( G ) Immunofluorescence images and quantification of β-catenin ( green ) in corneal sections from WT and Sparc −/− mice at different postinjury time points; nuclei were counterstained with DAPI ( blue ) ( n = 5 mice per group). ( H , I ) Scratch-wound assay and quantification of wound closure in HCECs after β-catenin knockdown with or without exogenous SPARC supplementation (the knockdown efficiency of β-catenin in HCECs is shown in B; n = 5 independent experiments per group). Scale bars are indicated in the images. Data are presented as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001.
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rabbit anti c myctag mab  (ABclonal Biotechnology)
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SPARC knockdown disrupts Wnt signaling and β-catenin nuclear translocation. ( A , B ) Western blot and RT-qPCR analysis showing reduced β-catenin <t>and</t> <t>c-Myc</t> protein and mRNA expression in HCECs following SPARC knockdown ( n = 5 independent experiments per group). ( C , D ) Western blot and RT-qPCR analysis of β-catenin protein and mRNA expression in corneal epithelial cells from WT and Sparc −/− mice at the indicated postinjury time points ( n = 3 independent pooled biological replicates per group). ( E , F ) Immunofluorescence staining of β-catenin ( red ) and DAPI ( blue ) in HCECs after SPARC knockdown ( n = 5 independent experiments per group). ( G ) Immunofluorescence images and quantification of β-catenin ( green ) in corneal sections from WT and Sparc −/− mice at different postinjury time points; nuclei were counterstained with DAPI ( blue ) ( n = 5 mice per group). ( H , I ) Scratch-wound assay and quantification of wound closure in HCECs after β-catenin knockdown with or without exogenous SPARC supplementation (the knockdown efficiency of β-catenin in HCECs is shown in B; n = 5 independent experiments per group). Scale bars are indicated in the images. Data are presented as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001.
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rabbit anti myc  (ABclonal Biotechnology)
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SPARC knockdown disrupts Wnt signaling and β-catenin nuclear translocation. ( A , B ) Western blot and RT-qPCR analysis showing reduced β-catenin <t>and</t> <t>c-Myc</t> protein and mRNA expression in HCECs following SPARC knockdown ( n = 5 independent experiments per group). ( C , D ) Western blot and RT-qPCR analysis of β-catenin protein and mRNA expression in corneal epithelial cells from WT and Sparc −/− mice at the indicated postinjury time points ( n = 3 independent pooled biological replicates per group). ( E , F ) Immunofluorescence staining of β-catenin ( red ) and DAPI ( blue ) in HCECs after SPARC knockdown ( n = 5 independent experiments per group). ( G ) Immunofluorescence images and quantification of β-catenin ( green ) in corneal sections from WT and Sparc −/− mice at different postinjury time points; nuclei were counterstained with DAPI ( blue ) ( n = 5 mice per group). ( H , I ) Scratch-wound assay and quantification of wound closure in HCECs after β-catenin knockdown with or without exogenous SPARC supplementation (the knockdown efficiency of β-catenin in HCECs is shown in B; n = 5 independent experiments per group). Scale bars are indicated in the images. Data are presented as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001.
Rabbit Anti Myc, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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anti myc  (ABclonal Biotechnology)
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SPARC knockdown disrupts Wnt signaling and β-catenin nuclear translocation. ( A , B ) Western blot and RT-qPCR analysis showing reduced β-catenin <t>and</t> <t>c-Myc</t> protein and mRNA expression in HCECs following SPARC knockdown ( n = 5 independent experiments per group). ( C , D ) Western blot and RT-qPCR analysis of β-catenin protein and mRNA expression in corneal epithelial cells from WT and Sparc −/− mice at the indicated postinjury time points ( n = 3 independent pooled biological replicates per group). ( E , F ) Immunofluorescence staining of β-catenin ( red ) and DAPI ( blue ) in HCECs after SPARC knockdown ( n = 5 independent experiments per group). ( G ) Immunofluorescence images and quantification of β-catenin ( green ) in corneal sections from WT and Sparc −/− mice at different postinjury time points; nuclei were counterstained with DAPI ( blue ) ( n = 5 mice per group). ( H , I ) Scratch-wound assay and quantification of wound closure in HCECs after β-catenin knockdown with or without exogenous SPARC supplementation (the knockdown efficiency of β-catenin in HCECs is shown in B; n = 5 independent experiments per group). Scale bars are indicated in the images. Data are presented as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001.
Anti Myc, supplied by ABclonal Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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rabbit anti myc tag pab  (Huabio Inc)
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Huabio Inc rabbit anti myc tag pab
Validate the interaction between host proteins and Gp CDT based on Co-IP. (A) The Gp CDT-His protein (2μg) was immunoprecipitated with anti-His-tag mAb, and the EPHB4 or (B) ITGA5, (C) APP, (D) UGCG, (E) GOLGA7 was specifically <t>detected</t> <t>with</t> <t>anti-Myc-tag</t> pAb. (F) The LITAF or (G) TM9SF4, (H) SLC12A4, (I) SEC63 whole-cell lysates (200μL) was immunoprecipitated with anti-Myc-tag pAb, and the Gp CDT-His was specifically detected with anti-His-tag mAb.
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Image Search Results


SPARC knockdown disrupts Wnt signaling and β-catenin nuclear translocation. ( A , B ) Western blot and RT-qPCR analysis showing reduced β-catenin and c-Myc protein and mRNA expression in HCECs following SPARC knockdown ( n = 5 independent experiments per group). ( C , D ) Western blot and RT-qPCR analysis of β-catenin protein and mRNA expression in corneal epithelial cells from WT and Sparc −/− mice at the indicated postinjury time points ( n = 3 independent pooled biological replicates per group). ( E , F ) Immunofluorescence staining of β-catenin ( red ) and DAPI ( blue ) in HCECs after SPARC knockdown ( n = 5 independent experiments per group). ( G ) Immunofluorescence images and quantification of β-catenin ( green ) in corneal sections from WT and Sparc −/− mice at different postinjury time points; nuclei were counterstained with DAPI ( blue ) ( n = 5 mice per group). ( H , I ) Scratch-wound assay and quantification of wound closure in HCECs after β-catenin knockdown with or without exogenous SPARC supplementation (the knockdown efficiency of β-catenin in HCECs is shown in B; n = 5 independent experiments per group). Scale bars are indicated in the images. Data are presented as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001.

Journal: Investigative Ophthalmology & Visual Science

Article Title: SPARC Promotes Corneal Epithelial Wound Healing Through β-catenin Nuclear Translocation and c-Met Activation

doi: 10.1167/iovs.67.10.23

Figure Lengend Snippet: SPARC knockdown disrupts Wnt signaling and β-catenin nuclear translocation. ( A , B ) Western blot and RT-qPCR analysis showing reduced β-catenin and c-Myc protein and mRNA expression in HCECs following SPARC knockdown ( n = 5 independent experiments per group). ( C , D ) Western blot and RT-qPCR analysis of β-catenin protein and mRNA expression in corneal epithelial cells from WT and Sparc −/− mice at the indicated postinjury time points ( n = 3 independent pooled biological replicates per group). ( E , F ) Immunofluorescence staining of β-catenin ( red ) and DAPI ( blue ) in HCECs after SPARC knockdown ( n = 5 independent experiments per group). ( G ) Immunofluorescence images and quantification of β-catenin ( green ) in corneal sections from WT and Sparc −/− mice at different postinjury time points; nuclei were counterstained with DAPI ( blue ) ( n = 5 mice per group). ( H , I ) Scratch-wound assay and quantification of wound closure in HCECs after β-catenin knockdown with or without exogenous SPARC supplementation (the knockdown efficiency of β-catenin in HCECs is shown in B; n = 5 independent experiments per group). Scale bars are indicated in the images. Data are presented as mean ± SD. * P < 0.05, *** P < 0.001, **** P < 0.0001.

Article Snippet: The primary antibodies used were anti-SPARC ( AB290636 ; Abcam), anti–β-catenin (A19657; ABclonal), anti–p-Met (3077; CST), anti–c-Met (25869-1-AP; Proteintech, Rosemont, IL, USA), anti–cellular myelocytomatosis oncogene (c-Myc) (A1309; ABclonal), anti–T-cell factor (TCF) 4 (A1141; ABclonal), and anti-GAPDH (A19056; ABclonal).

Techniques: Knockdown, Translocation Assay, Western Blot, Quantitative RT-PCR, Expressing, Immunofluorescence, Staining, Scratch Wound Assay Assay

Validate the interaction between host proteins and Gp CDT based on Co-IP. (A) The Gp CDT-His protein (2μg) was immunoprecipitated with anti-His-tag mAb, and the EPHB4 or (B) ITGA5, (C) APP, (D) UGCG, (E) GOLGA7 was specifically detected with anti-Myc-tag pAb. (F) The LITAF or (G) TM9SF4, (H) SLC12A4, (I) SEC63 whole-cell lysates (200μL) was immunoprecipitated with anti-Myc-tag pAb, and the Gp CDT-His was specifically detected with anti-His-tag mAb.

Journal: Frontiers in Cellular and Infection Microbiology

Article Title: TM9SF4 acts as a receptor mediating Glaesserella parasuis cytolethal distending toxin–induced cytotoxicity in PK15 cells

doi: 10.3389/fcimb.2026.1783709

Figure Lengend Snippet: Validate the interaction between host proteins and Gp CDT based on Co-IP. (A) The Gp CDT-His protein (2μg) was immunoprecipitated with anti-His-tag mAb, and the EPHB4 or (B) ITGA5, (C) APP, (D) UGCG, (E) GOLGA7 was specifically detected with anti-Myc-tag pAb. (F) The LITAF or (G) TM9SF4, (H) SLC12A4, (I) SEC63 whole-cell lysates (200μL) was immunoprecipitated with anti-Myc-tag pAb, and the Gp CDT-His was specifically detected with anti-His-tag mAb.

Article Snippet: Pre-washed Protein A/G Magnetic Beads (50 μL) were resuspended in 200 μL cold PBS along with either mouse anti-His-Tag mAb (1:100, ABclonal, China) or rabbit anti-Myc-tag pAb (1:200, HUABIO, China).

Techniques: Co-Immunoprecipitation Assay, Immunoprecipitation