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ha tag  (Proteintech)


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    Structured Review

    Proteintech ha tag
    Ha Tag, supplied by Proteintech, used in various techniques. Bioz Stars score: 96/100, based on 1676 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/ha+51064+2+ap/HA+Tag+Antibody/pmc13010945-36-9-66
    Average 96 stars, based on 1676 article reviews
    ha tag - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Aqueous Normal-phase Chromatography:

    Article Title: TRIM40 Drives Pathological Cardiac Hypertrophy and Heart Failure via Ubiquitination of PKN2.
    Article Snippet: AAV9-TRIM40, EV, AAV9-cTNT-TRIM40, and AAV9cTNT-NC were obtained from Genechem (Shanghai, China). .. Antibodies against TRIM40 (24526-1-AP), MYH7 (22280-1-AP), ANP (27426-1-AP), BNP (13299-1-AP), PKN2 (14608-1-AP), cTnT (68300-1-Ig), Rabbit IgG (B900610), His (6005-1-lg), Flag (20543-1- P) and HA (51064-2-AP) were purchased from Proteintech (IL, USA). .. Antibodies against alpha actinin (ab68167), and vimentin (ab8978) were obtained from Abcam (Cambridge, UK).

    Article Title: TRIM40 Drives Pathological Cardiac Hypertrophy and Heart Failure via Ubiquitination of PKN2
    Article Snippet: AAV9‐TRIM40, EV, AAV9‐cTNT‐TRIM40, and AAV9‐cTNT‐NC were obtained from Genechem (Shanghai, China). .. Antibodies against TRIM40 (24526‐1‐AP), MYH7 (22280‐1‐AP), ANP (27426‐1‐AP), BNP (13299‐1‐AP), PKN2 (14608‐1‐AP), cTnT (68300‐1‐Ig), Rabbit IgG (B900610), His (6005‐1‐lg), Flag (20543‐1‐AP) and HA (51064‐2‐AP) were purchased from Proteintech (IL, USA). .. Antibodies against alpha actinin (ab68167), and vimentin (ab8978) were obtained from Abcam (Cambridge, UK).

    other:

    Article Title: Zinc finger protein ZNF33B facilitates Japanese encephalitis virus replication by regulating m 6 A modification on Ifih1 and Irf3 transcripts to antagonize antiviral response.
    Article Snippet: The antibodies probed by GAPDH (Cat. # 60004-1-Ig), IgG (Cat. # 30000-0-AP), FLAG (Cat. # 20543-1-AP), HA (Cat. # 51064-2-AP, 66006-2-Ig), RIG-I (Cat. # 20566-1-AP), MDA5 (Cat. # 21775-1-AP), TBK1 (Cat. # 283971-1-AP), METTL14 (Cat. # 26158-1-AP), YTHDC1 (Cat. # 14392-1-AP), YTHDF2 (Cat. # 24744-1- AP) and m6A (Cat. # 68055-1-Ig) were obtained from Proteintech (USA).

    Article Title: Zinc finger protein ZNF33B facilitates Japanese encephalitis virus replication by regulating m 6 A modification on Ifih1 and Irf3 transcripts to antagonize antiviral response
    Article Snippet: The antibodies probed by GAPDH (Cat. # 60004-1-Ig), IgG (Cat. # 30000-0-AP), FLAG (Cat. # 20543-1-AP), HA (Cat. # 51064-2-AP, 66006-2-Ig), RIG-I (Cat. # 20566-1-AP), MDA5 (Cat. # 21775-1-AP), TBK1 (Cat. # 283971-1-AP), METTL14 (Cat. # 26158-1-AP), YTHDC1 (Cat. # 14392-1-AP), YTHDF2 (Cat. # 24744-1-AP) and m6A (Cat. # 68055-1-Ig) were obtained from Proteintech (USA).



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    eIF3m interacted with FAdV-4 ORF1B protein in LMH cells. (A and B) eIF3m interacted with exogenous ORF1B. LMH cells co-transfected with 1 μg/well of p3 × flag-ORF1B and 1 μg/well pCAGGS-HA-eIF3m were lysed at 48 h, and cell lysates were immunoprecipitated with an anti-flag (A) or <t>anti-HA</t> (B) antibody followed by western blot with anti-HA and anti-flag antibodies. (C) The interaction of eIF3m with endogenous ORF1B. LMH cells transfected with 1 μg/well of pCAGGS-HA-eIF3m or empty vector were infected with CH/HNJZ/2015 at an MOI of 0.01 at 24 hpt. Cell lysates were immunoprecipitated with an anti-HA antibody followed by western blot with anti-HA and anti-ORF1B antibodies. (D) eIF3m and ORF1B were co-localized in cytoplasm. LMH cell co-transfected with 1 μg/well of pEGFP-ORF1B and 1 μg/well of pDsRed-eIF3m were fixed at 24 h. After stained with DAPI, the fluorescence was observed by using a confocal microscope.
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    LMO7 promotes K48-linked polyubiquitination of MGMT . A , HEK293T cells expressing FLAG-MGMT were cotransfected with HA-ubiquitin WT (HA-Ub WT) or lysine-specific mutants (K48R or K48-only) and treated with MG132 (5 μM, overnight); MGMT ubiquitination was examined under denaturing conditions by immunoprecipitation (IP) with anti-FLAG M2-agarose beads followed by Western blotting (WB) with <t>anti-HA.</t> B , overexpression of LMO7-WT, but not the F-box–deficient mutant LMO7b, increased MGMT ubiquitination in HEK293T cells coexpressing FLAG-MGMT and HA-Ub after MG132 treatment (5 μM, overnight). C , LMO7 knockdown using two independent shRNAs reduced MGMT ubiquitination in HEK293T cells treated with MG132 (5 μM, overnight); knockdown efficiency was confirmed by WB. D , in H1299 cells, LMO7-WT, but not LMO7b, enhanced K48-linked MGMT ubiquitination detected using Halo-TUBE beads (K48-specific) under denaturing conditions following MG132 treatment (5 μM, overnight). E , LMO7 knockdown diminished K48-linked MGMT ubiquitination in H1299 cells, analyzed as in ( D ). Data are representative of n ≥ 3 biological replicates. HA, hemagglutinin; HEK293T, human embryonic kidney 293T cell line; LMO7, LIM domain only 7; MGMT, O 6 -methylguanine-DNA methyltransferase.
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    LMO7 promotes K48-linked polyubiquitination of MGMT . A , HEK293T cells expressing FLAG-MGMT were cotransfected with HA-ubiquitin WT (HA-Ub WT) or lysine-specific mutants (K48R or K48-only) and treated with MG132 (5 μM, overnight); MGMT ubiquitination was examined under denaturing conditions by immunoprecipitation (IP) with anti-FLAG M2-agarose beads followed by Western blotting (WB) with <t>anti-HA.</t> B , overexpression of LMO7-WT, but not the F-box–deficient mutant LMO7b, increased MGMT ubiquitination in HEK293T cells coexpressing FLAG-MGMT and HA-Ub after MG132 treatment (5 μM, overnight). C , LMO7 knockdown using two independent shRNAs reduced MGMT ubiquitination in HEK293T cells treated with MG132 (5 μM, overnight); knockdown efficiency was confirmed by WB. D , in H1299 cells, LMO7-WT, but not LMO7b, enhanced K48-linked MGMT ubiquitination detected using Halo-TUBE beads (K48-specific) under denaturing conditions following MG132 treatment (5 μM, overnight). E , LMO7 knockdown diminished K48-linked MGMT ubiquitination in H1299 cells, analyzed as in ( D ). Data are representative of n ≥ 3 biological replicates. HA, hemagglutinin; HEK293T, human embryonic kidney 293T cell line; LMO7, LIM domain only 7; MGMT, O 6 -methylguanine-DNA methyltransferase.
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    LMO7 promotes K48-linked polyubiquitination of MGMT . A , HEK293T cells expressing FLAG-MGMT were cotransfected with HA-ubiquitin WT (HA-Ub WT) or lysine-specific mutants (K48R or K48-only) and treated with MG132 (5 μM, overnight); MGMT ubiquitination was examined under denaturing conditions by immunoprecipitation (IP) with anti-FLAG M2-agarose beads followed by Western blotting (WB) with <t>anti-HA.</t> B , overexpression of LMO7-WT, but not the F-box–deficient mutant LMO7b, increased MGMT ubiquitination in HEK293T cells coexpressing FLAG-MGMT and HA-Ub after MG132 treatment (5 μM, overnight). C , LMO7 knockdown using two independent shRNAs reduced MGMT ubiquitination in HEK293T cells treated with MG132 (5 μM, overnight); knockdown efficiency was confirmed by WB. D , in H1299 cells, LMO7-WT, but not LMO7b, enhanced K48-linked MGMT ubiquitination detected using Halo-TUBE beads (K48-specific) under denaturing conditions following MG132 treatment (5 μM, overnight). E , LMO7 knockdown diminished K48-linked MGMT ubiquitination in H1299 cells, analyzed as in ( D ). Data are representative of n ≥ 3 biological replicates. HA, hemagglutinin; HEK293T, human embryonic kidney 293T cell line; LMO7, LIM domain only 7; MGMT, O 6 -methylguanine-DNA methyltransferase.
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    Image Search Results


    eIF3m interacted with FAdV-4 ORF1B protein in LMH cells. (A and B) eIF3m interacted with exogenous ORF1B. LMH cells co-transfected with 1 μg/well of p3 × flag-ORF1B and 1 μg/well pCAGGS-HA-eIF3m were lysed at 48 h, and cell lysates were immunoprecipitated with an anti-flag (A) or anti-HA (B) antibody followed by western blot with anti-HA and anti-flag antibodies. (C) The interaction of eIF3m with endogenous ORF1B. LMH cells transfected with 1 μg/well of pCAGGS-HA-eIF3m or empty vector were infected with CH/HNJZ/2015 at an MOI of 0.01 at 24 hpt. Cell lysates were immunoprecipitated with an anti-HA antibody followed by western blot with anti-HA and anti-ORF1B antibodies. (D) eIF3m and ORF1B were co-localized in cytoplasm. LMH cell co-transfected with 1 μg/well of pEGFP-ORF1B and 1 μg/well of pDsRed-eIF3m were fixed at 24 h. After stained with DAPI, the fluorescence was observed by using a confocal microscope.

    Journal: Poultry Science

    Article Title: eIF3m promotes fowl adenovirus serotype 4 replication via interacting with ORF1B protein

    doi: 10.1016/j.psj.2026.106566

    Figure Lengend Snippet: eIF3m interacted with FAdV-4 ORF1B protein in LMH cells. (A and B) eIF3m interacted with exogenous ORF1B. LMH cells co-transfected with 1 μg/well of p3 × flag-ORF1B and 1 μg/well pCAGGS-HA-eIF3m were lysed at 48 h, and cell lysates were immunoprecipitated with an anti-flag (A) or anti-HA (B) antibody followed by western blot with anti-HA and anti-flag antibodies. (C) The interaction of eIF3m with endogenous ORF1B. LMH cells transfected with 1 μg/well of pCAGGS-HA-eIF3m or empty vector were infected with CH/HNJZ/2015 at an MOI of 0.01 at 24 hpt. Cell lysates were immunoprecipitated with an anti-HA antibody followed by western blot with anti-HA and anti-ORF1B antibodies. (D) eIF3m and ORF1B were co-localized in cytoplasm. LMH cell co-transfected with 1 μg/well of pEGFP-ORF1B and 1 μg/well of pDsRed-eIF3m were fixed at 24 h. After stained with DAPI, the fluorescence was observed by using a confocal microscope.

    Article Snippet: Commercial antibodies used in this study included rabbit anti-flag monoclonal antibody (240568AA1, proteintech), mouse anti-HA monoclonal antibody (66006-2-Ig, proteintech), rabbit anti-GAPDH monoclonal antibody (A19056, ABclonal).

    Techniques: Transfection, Immunoprecipitation, Western Blot, Plasmid Preparation, Infection, Staining, Fluorescence, Microscopy

    LMO7 promotes K48-linked polyubiquitination of MGMT . A , HEK293T cells expressing FLAG-MGMT were cotransfected with HA-ubiquitin WT (HA-Ub WT) or lysine-specific mutants (K48R or K48-only) and treated with MG132 (5 μM, overnight); MGMT ubiquitination was examined under denaturing conditions by immunoprecipitation (IP) with anti-FLAG M2-agarose beads followed by Western blotting (WB) with anti-HA. B , overexpression of LMO7-WT, but not the F-box–deficient mutant LMO7b, increased MGMT ubiquitination in HEK293T cells coexpressing FLAG-MGMT and HA-Ub after MG132 treatment (5 μM, overnight). C , LMO7 knockdown using two independent shRNAs reduced MGMT ubiquitination in HEK293T cells treated with MG132 (5 μM, overnight); knockdown efficiency was confirmed by WB. D , in H1299 cells, LMO7-WT, but not LMO7b, enhanced K48-linked MGMT ubiquitination detected using Halo-TUBE beads (K48-specific) under denaturing conditions following MG132 treatment (5 μM, overnight). E , LMO7 knockdown diminished K48-linked MGMT ubiquitination in H1299 cells, analyzed as in ( D ). Data are representative of n ≥ 3 biological replicates. HA, hemagglutinin; HEK293T, human embryonic kidney 293T cell line; LMO7, LIM domain only 7; MGMT, O 6 -methylguanine-DNA methyltransferase.

    Journal: The Journal of Biological Chemistry

    Article Title: E3 ligase LMO7 enhances temozolomide sensitivity by promoting MGMT degradation in lung cancer

    doi: 10.1016/j.jbc.2026.111331

    Figure Lengend Snippet: LMO7 promotes K48-linked polyubiquitination of MGMT . A , HEK293T cells expressing FLAG-MGMT were cotransfected with HA-ubiquitin WT (HA-Ub WT) or lysine-specific mutants (K48R or K48-only) and treated with MG132 (5 μM, overnight); MGMT ubiquitination was examined under denaturing conditions by immunoprecipitation (IP) with anti-FLAG M2-agarose beads followed by Western blotting (WB) with anti-HA. B , overexpression of LMO7-WT, but not the F-box–deficient mutant LMO7b, increased MGMT ubiquitination in HEK293T cells coexpressing FLAG-MGMT and HA-Ub after MG132 treatment (5 μM, overnight). C , LMO7 knockdown using two independent shRNAs reduced MGMT ubiquitination in HEK293T cells treated with MG132 (5 μM, overnight); knockdown efficiency was confirmed by WB. D , in H1299 cells, LMO7-WT, but not LMO7b, enhanced K48-linked MGMT ubiquitination detected using Halo-TUBE beads (K48-specific) under denaturing conditions following MG132 treatment (5 μM, overnight). E , LMO7 knockdown diminished K48-linked MGMT ubiquitination in H1299 cells, analyzed as in ( D ). Data are representative of n ≥ 3 biological replicates. HA, hemagglutinin; HEK293T, human embryonic kidney 293T cell line; LMO7, LIM domain only 7; MGMT, O 6 -methylguanine-DNA methyltransferase.

    Article Snippet: The following primary antibodies were used: anti-MGMT (17195-1-AP, Proteintech), anti-HA (51064-2-AP, Proteintech), anti-LMO7 (ab224113, Abcam), anti-FLAG (F3165, Sigma–Aldrich), and anti-ubiquitin (sc-8017, Santa Cruz Biotechnology).

    Techniques: Expressing, Ubiquitin Proteomics, Immunoprecipitation, Western Blot, Over Expression, Mutagenesis, Knockdown