Takara Bio

RetroNectin (Recombinant Human Fibronectin Fragment)

#T100A · transduction

37
Citing papers
470
Combined citations
Supplier page Find this product

Research areas

CAR-T cell therapy research21Immune Cell Function and Interaction9Virus-based gene therapy research6Immunotherapy and Immune Responses6Viral Infectious Diseases and Gene Expression in Insects6Cancer Immunotherapy and Biomarkers5Acute Myeloid Leukemia Research4Monoclonal and Polyclonal Antibodies Research3

Papers citing this product

1
Hectd3 promotes pathogenic Th17 lineage through Stat3 activation and Malt1 signaling in neuroinflammation
Nature Communications·2019·85 cit.·DOI
2
Potent ex vivo armed T cells using recombinant bispecific antibodies for adoptive immunotherapy with reduced cytokine release
Journal for ImmunoTherapy of Cancer·2021·47 cit.·DOI
3
Promoter choice: Who should drive the CAR in T cells?
PLoS ONE·2020·45 cit.·DOI
4
Obesity-induced galectin-9 is a therapeutic target in B-cell acute lymphoblastic leukemia
Nature Communications·2022·37 cit.·DOI
5
B7-H3 specific CAR-T cells exhibit potent activity against prostate cancer
Cell Death Discovery·2023·35 cit.·DOI
6
Dual targeting ovarian cancer by Muc16 CAR T cells secreting a bispecific T cell engager antibody for an intracellular tumor antigen WT1
Cancer Immunology Immunotherapy·2023·34 cit.·DOI
7
miR-130b and miR-128a are essential lineage-specific codrivers of t(4;11) MLL-AF4 acute leukemia
Blood·2021·33 cit.·DOI
8
Establishment of a novel platform cell line for efficient and precise evaluation of T cell receptor functional avidity
Oncotarget·2018·21 cit.·DOI
9
Humanization of the antigen-recognition domain does not impinge on the antigen-binding, cytokine secretion, and antitumor reactivity of humanized nanobody-based CD19-redirected CAR-T cells
Journal of Translational Medicine·2024·18 cit.·DOI
10
Cullin-5 deficiency promotes chimeric antigen receptor T cell effector functions potentially via the modulation of JAK/STAT signaling pathway
Nature Communications·2024·17 cit.·DOI

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