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tcl1a  (Novus Biologicals)


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    Structured Review

    Novus Biologicals tcl1a
    Tcl1a, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 93/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tcl1a/TCL1A+Antibody+(TCL1%2F2078)/pm39985963-108-32-35
    Average 93 stars, based on 2 article reviews
    tcl1a - by Bioz Stars, 2026-09
    93/100 stars

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    Related Articles

    Incubation:

    Article Title: TCL1A Single-Nucleotide Polymorphisms and Estrogen-Mediated Toll-Like Receptor-MYD88–Dependent Nuclear Factor- κ B Activation: Single-Nucleotide Polymorphism– and Selective Estrogen Receptor Modulator–Dependent Modification of Inflammation and Immune Response
    Article Snippet: .. The membranes were incubated overnight with primary antibodies: TCL1A, TLR2, TLR7, TLR9, TLR10, MYD88, UNC93B1 (Novus Biologicals, Littleton, CO), and ACTB at a 1:500 dilution at 4°C. .. The washed membranes were then incubated with goat anti-rabbit or anti-mouse secondary antibody (Santa Cruz Biotechnology, Dallas, TX) at a 1:20,000 dilution.

    Immunofluorescence:

    Article Title: Single-cell transcriptomics reveals the immune mechanisms by which tonsillectomy improves clinical outcomes of recurrent Immuoglobulin A nephropathy after kidney transplant.
    Article Snippet: Immunoglobulin A nephropathy recurrence (IgANR) is a major cause of graft function loss in renal transplant patients with IgA nephropathy.. Tonsillectomy has been recognized as an effective treatment for IgANR, but the cellular and molecular effects underlying its efficacy remain poorly understood.. We aimed to identify the cell types and gene expression profiles in tonsillar tissue and peripheral blood mononuclear cells (PBMCs) to investigate the effectiveness of tonsillectomy in IgANR treatment.



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    Image Search Results


    A strong correlation between TCL1A and AML was identified by Mendelian randomization. A Forest plot of the top five plasma proteins most associated with AML. Scatter plots of B ADGRF5, C FLRT2, D GRAP2, E PPIC, and F TCL1A with AML. G Volcano plot showing the relationship between plasma proteins and AML. Note: AML: acute myelogenous leukemia

    Journal: BMC Cancer

    Article Title: New drug targets for acute myeloid leukemia identified through a comprehensive analysis of the plasma protein

    doi: 10.1186/s12885-025-15438-5

    Figure Lengend Snippet: A strong correlation between TCL1A and AML was identified by Mendelian randomization. A Forest plot of the top five plasma proteins most associated with AML. Scatter plots of B ADGRF5, C FLRT2, D GRAP2, E PPIC, and F TCL1A with AML. G Volcano plot showing the relationship between plasma proteins and AML. Note: AML: acute myelogenous leukemia

    Article Snippet: The membranes were incubated overnight with primary antibodies against TCL1A (Proteintech, #10,475–1-AP), β-actin (Cell Signaling Technology (CST), #4970).

    Techniques: Clinical Proteomics

    TCL1A-eqTL showed a significant positive association with AML by Mendelian randomization. A Chromosomal localization of TCL1A. B Forest plot, C scatter plots, D leave-one-out plot, and E funnel plots of TCL1A-eqTL and AML. F Bayesian co-localization analysis between TCL1A-eqTL and AML. Note: AML: acute myelogenous leukemia

    Journal: BMC Cancer

    Article Title: New drug targets for acute myeloid leukemia identified through a comprehensive analysis of the plasma protein

    doi: 10.1186/s12885-025-15438-5

    Figure Lengend Snippet: TCL1A-eqTL showed a significant positive association with AML by Mendelian randomization. A Chromosomal localization of TCL1A. B Forest plot, C scatter plots, D leave-one-out plot, and E funnel plots of TCL1A-eqTL and AML. F Bayesian co-localization analysis between TCL1A-eqTL and AML. Note: AML: acute myelogenous leukemia

    Article Snippet: The membranes were incubated overnight with primary antibodies against TCL1A (Proteintech, #10,475–1-AP), β-actin (Cell Signaling Technology (CST), #4970).

    Techniques:

    Expression differences of TCL1A. A ROC curves for TCL1A. B Differences in TCL1A expression between AML patients and healthy donors, and differences in TCL1A expression in subgroups by C , D age, E sex, F WBC count, G BM blast percentage, H PB blast percentage, I Cytogenetic risk, J FAB classifications, K Cytogenetics, L FLT3 mutation, M RAS mutation, N IDH1 R132 mutation, and O NPM1 mutation. Note: AML: acute myelogenous leukemia; WBC: white blood cell; BM: bone marrow; PB: peripheral blood. * p < 0.05, ** p < 0.01, *** p < 0.001

    Journal: BMC Cancer

    Article Title: New drug targets for acute myeloid leukemia identified through a comprehensive analysis of the plasma protein

    doi: 10.1186/s12885-025-15438-5

    Figure Lengend Snippet: Expression differences of TCL1A. A ROC curves for TCL1A. B Differences in TCL1A expression between AML patients and healthy donors, and differences in TCL1A expression in subgroups by C , D age, E sex, F WBC count, G BM blast percentage, H PB blast percentage, I Cytogenetic risk, J FAB classifications, K Cytogenetics, L FLT3 mutation, M RAS mutation, N IDH1 R132 mutation, and O NPM1 mutation. Note: AML: acute myelogenous leukemia; WBC: white blood cell; BM: bone marrow; PB: peripheral blood. * p < 0.05, ** p < 0.01, *** p < 0.001

    Article Snippet: The membranes were incubated overnight with primary antibodies against TCL1A (Proteintech, #10,475–1-AP), β-actin (Cell Signaling Technology (CST), #4970).

    Techniques: Expressing, Mutagenesis

    High TCL1A expression was linked to poor prognosis in AML patients through bioinformatics analysis. A KM analysis of AML patients and subgroups by karyotype: B good, C intermediate, D poor; FAB classification: E M0, F M1, G M2, H M3, I M4, J M5, G M6; L untreated and M chemotherapy stratified; and molecular risk classification: N IDH1 mutation, O IDH2 mutation, P NPM1 mutation, Q , R FLT3 mutation, S NRAS mutation, T CEBPA mutation. Note: AML: acute myelogenous leukemia; KM analysis: Kaplan–Meier analysis; FAB: French-American-British classification

    Journal: BMC Cancer

    Article Title: New drug targets for acute myeloid leukemia identified through a comprehensive analysis of the plasma protein

    doi: 10.1186/s12885-025-15438-5

    Figure Lengend Snippet: High TCL1A expression was linked to poor prognosis in AML patients through bioinformatics analysis. A KM analysis of AML patients and subgroups by karyotype: B good, C intermediate, D poor; FAB classification: E M0, F M1, G M2, H M3, I M4, J M5, G M6; L untreated and M chemotherapy stratified; and molecular risk classification: N IDH1 mutation, O IDH2 mutation, P NPM1 mutation, Q , R FLT3 mutation, S NRAS mutation, T CEBPA mutation. Note: AML: acute myelogenous leukemia; KM analysis: Kaplan–Meier analysis; FAB: French-American-British classification

    Article Snippet: The membranes were incubated overnight with primary antibodies against TCL1A (Proteintech, #10,475–1-AP), β-actin (Cell Signaling Technology (CST), #4970).

    Techniques: Expressing, Molecular Risk, Mutagenesis

    The expression of TCL1A is highly specific in tissues and cell lines. A The mutational landscape of TCL1A in the genome of AML. Distribution of TCL1A expression in B tissues and C cell lines. D The IHC results of TCL1A in different tumor types, showing its subcellular localization. Note: AML: acute myelogenous leukemia; IHC: immunohistochemistry

    Journal: BMC Cancer

    Article Title: New drug targets for acute myeloid leukemia identified through a comprehensive analysis of the plasma protein

    doi: 10.1186/s12885-025-15438-5

    Figure Lengend Snippet: The expression of TCL1A is highly specific in tissues and cell lines. A The mutational landscape of TCL1A in the genome of AML. Distribution of TCL1A expression in B tissues and C cell lines. D The IHC results of TCL1A in different tumor types, showing its subcellular localization. Note: AML: acute myelogenous leukemia; IHC: immunohistochemistry

    Article Snippet: The membranes were incubated overnight with primary antibodies against TCL1A (Proteintech, #10,475–1-AP), β-actin (Cell Signaling Technology (CST), #4970).

    Techniques: Expressing, Immunohistochemistry

    Potential therapeutic agents for TCL1A identified through virtual screening. A Potential therapeutic agents for TCL1A were screened using HTVS and B sorted according to docking scores. ( C ) Compounds satisfying all three criteria. Note: HTVS: high-throughput virtual screening

    Journal: BMC Cancer

    Article Title: New drug targets for acute myeloid leukemia identified through a comprehensive analysis of the plasma protein

    doi: 10.1186/s12885-025-15438-5

    Figure Lengend Snippet: Potential therapeutic agents for TCL1A identified through virtual screening. A Potential therapeutic agents for TCL1A were screened using HTVS and B sorted according to docking scores. ( C ) Compounds satisfying all three criteria. Note: HTVS: high-throughput virtual screening

    Article Snippet: The membranes were incubated overnight with primary antibodies against TCL1A (Proteintech, #10,475–1-AP), β-actin (Cell Signaling Technology (CST), #4970).

    Techniques: High Throughput Screening Assay

    Molecular docking shows high binding affinity between small molecule compounds and TCL1A. Prediction and visualization of the interaction force between A 0449–0045, B N060-0154, C 2292159–89–6, D N025-0034, E N025-0034, F 0120–0021, G 0827–0413, H 8002–5894, I 3731–0092, J 8020–8702, and TCL1A, respectively

    Journal: BMC Cancer

    Article Title: New drug targets for acute myeloid leukemia identified through a comprehensive analysis of the plasma protein

    doi: 10.1186/s12885-025-15438-5

    Figure Lengend Snippet: Molecular docking shows high binding affinity between small molecule compounds and TCL1A. Prediction and visualization of the interaction force between A 0449–0045, B N060-0154, C 2292159–89–6, D N025-0034, E N025-0034, F 0120–0021, G 0827–0413, H 8002–5894, I 3731–0092, J 8020–8702, and TCL1A, respectively

    Article Snippet: The membranes were incubated overnight with primary antibodies against TCL1A (Proteintech, #10,475–1-AP), β-actin (Cell Signaling Technology (CST), #4970).

    Techniques: Binding Assay

    Specific expression of TCL1A in leukemia cells and the potential therapeutic effect of Bletilloside A. A The expression levels of TCL1A mRNA in AML cells, normal bone marrow stromal cells, and other solid cancer cells. ( B RMSD, C Rg, D SASA, E HBonds, and F RMSF value of Bletilloside A-TCL1A complexes over time. Note: Normal bone marrow stromal cells are shown as black labels, AML cells as red labels, and solid tumor cells as blue labels; RMSD: root mean square deviation; RMSF: root mean square fluctuation; HBonds: hydrogen bonds; Rg: radius of gyration; SASA: solvent accessible surface area

    Journal: BMC Cancer

    Article Title: New drug targets for acute myeloid leukemia identified through a comprehensive analysis of the plasma protein

    doi: 10.1186/s12885-025-15438-5

    Figure Lengend Snippet: Specific expression of TCL1A in leukemia cells and the potential therapeutic effect of Bletilloside A. A The expression levels of TCL1A mRNA in AML cells, normal bone marrow stromal cells, and other solid cancer cells. ( B RMSD, C Rg, D SASA, E HBonds, and F RMSF value of Bletilloside A-TCL1A complexes over time. Note: Normal bone marrow stromal cells are shown as black labels, AML cells as red labels, and solid tumor cells as blue labels; RMSD: root mean square deviation; RMSF: root mean square fluctuation; HBonds: hydrogen bonds; Rg: radius of gyration; SASA: solvent accessible surface area

    Article Snippet: The membranes were incubated overnight with primary antibodies against TCL1A (Proteintech, #10,475–1-AP), β-actin (Cell Signaling Technology (CST), #4970).

    Techniques: Expressing, Solvent