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calumenin calu antibody  (ProSci Incorporated)


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    ProSci Incorporated calumenin calu antibody
    Calumenin Calu Antibody, supplied by ProSci Incorporated, 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/calumenin+calu+antibody/CALU+Antibody/vazquez_morales_javier_ivan__2022__identification_of_affinity_enriched_sperm_and_oocyte_plasma_membrane_proteins_and_biological-199-27-31
    Average 90 stars, based on 1 article reviews
    calumenin calu antibody - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Sequencing:

    Article Title: Identification of Affinity-enriched Sperm and Oocyte Plasma Membrane Proteins and Biological Relevance of Potential Candidates in In-vitro Fertilization
    Article Snippet: .. The selected antibodies were predicted to react with the pig after a sequence alignment analysis between the putative antigen and the protein of interest in the pig; Calumenin (CALU) antibody (14-405, ProSci, USA), Prominin 2 (PROM2) antibody (bs-5814r, Bioss Antibodies, USA), and Schlafen-like 1 (SLFNL1) antibody (bs-10360r, Bioss). ..



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    Fig. 5. CD133+ HUHPCs modulated the global protein profile in colon cells. (A) Differentially expressed proteins were identified by matrix assisted laser desorption ionization-time of flight/mass spectrometry (MALDI-TOF/MS). The distribution of all the differentially expressed protein spots in fluorescence DIGE gels is shown. (a) Merged images of the SW480/CD133− and SW480/CD133+ groups. (b) Merged images of the SW620/CD133− and SW620/CD133+ groups. Circles represent the differentially expressed protein master spots no. that had been successfully identified by MALDI-TOF/MS in SW480 cells (c) and in SW620 cells (d). (B) The expression of several identified proteins in SW480 (left) and SW620 (right) cells was detected using western blot analysis: MAP4K4, SDF-1, MMP9, <t>CALU,</t> PRPH, LZTS1 and GAMT.
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    Image Search Results


    Validation of CALU, EMT marker genes, CD3 and α-SMA in breast cancer samples. ( A ) IHC staining scores for CALU and EMT markers from 8 TNBC patients.( B and C ) IHC staining results of CALU, E-cadherin, N-cadherin, Vimentin and Snail1 in TNBC tissues. ( D ) IF staining results of CALU and CD3 in breast cancer tissue. ( E ) IF staining results of CALU and α-SMA in breast cancer tissue.**p< 0.01; ***p< 0.001.

    Journal: Journal of Inflammation Research

    Article Title: Pan-Cancer Screening and Validation of CALU’s Role in EMT Regulation and Tumor Microenvironment in Triple-Negative Breast Cancer

    doi: 10.2147/JIR.S477846

    Figure Lengend Snippet: Validation of CALU, EMT marker genes, CD3 and α-SMA in breast cancer samples. ( A ) IHC staining scores for CALU and EMT markers from 8 TNBC patients.( B and C ) IHC staining results of CALU, E-cadherin, N-cadherin, Vimentin and Snail1 in TNBC tissues. ( D ) IF staining results of CALU and CD3 in breast cancer tissue. ( E ) IF staining results of CALU and α-SMA in breast cancer tissue.**p< 0.01; ***p< 0.001.

    Article Snippet: Primary antibodies, including CALU (1:100, Rabbit, PTG, 17804-1-AP), α-SMA (1:400, Mouse, Boster BM0002), and CD3 (1:200, Mouse, PTG, 60181-1-Ig), were diluted with 5% BSA and applied to the sections, which were incubated overnight at 4°C.

    Techniques: Biomarker Discovery, Marker, Immunohistochemistry, Staining

    Fig. 5. CD133+ HUHPCs modulated the global protein profile in colon cells. (A) Differentially expressed proteins were identified by matrix assisted laser desorption ionization-time of flight/mass spectrometry (MALDI-TOF/MS). The distribution of all the differentially expressed protein spots in fluorescence DIGE gels is shown. (a) Merged images of the SW480/CD133− and SW480/CD133+ groups. (b) Merged images of the SW620/CD133− and SW620/CD133+ groups. Circles represent the differentially expressed protein master spots no. that had been successfully identified by MALDI-TOF/MS in SW480 cells (c) and in SW620 cells (d). (B) The expression of several identified proteins in SW480 (left) and SW620 (right) cells was detected using western blot analysis: MAP4K4, SDF-1, MMP9, CALU, PRPH, LZTS1 and GAMT.

    Journal: Carcinogenesis

    Article Title: Human CD133-positive hematopoietic progenitor cells initiate growth and metastasis of colorectal cancer cells.

    doi: 10.1093/carcin/bgu192

    Figure Lengend Snippet: Fig. 5. CD133+ HUHPCs modulated the global protein profile in colon cells. (A) Differentially expressed proteins were identified by matrix assisted laser desorption ionization-time of flight/mass spectrometry (MALDI-TOF/MS). The distribution of all the differentially expressed protein spots in fluorescence DIGE gels is shown. (a) Merged images of the SW480/CD133− and SW480/CD133+ groups. (b) Merged images of the SW620/CD133− and SW620/CD133+ groups. Circles represent the differentially expressed protein master spots no. that had been successfully identified by MALDI-TOF/MS in SW480 cells (c) and in SW620 cells (d). (B) The expression of several identified proteins in SW480 (left) and SW620 (right) cells was detected using western blot analysis: MAP4K4, SDF-1, MMP9, CALU, PRPH, LZTS1 and GAMT.

    Article Snippet: The membranes were then incubated overnight at 4°C with rabbit polyclonal antihuman antibodies to mitogen-activated protein 4 kinase 4 (MAP4K4), stromal cell-derived factor-1 (SDF-1), matrix metallopeptidase 9 (MMP9), calumenin (CALU), peripherin (PRPH), leucine zipper, putative tumour suppressor 1 (LZTS1) and guanidinoacetate methyltransferase (GAMT) (diluted 1:1000; Santa Cruz Laboratories, Santa Cruz, CA) and the mouse polyclonal antihuman glyceraldehyde 3-phosphate dehydrogenase antibody (diluted 1:2000; Epitomics Corporation).

    Techniques: Mass Spectrometry, Fluorescence, Expressing, Western Blot