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Enzo Biochem
anti-ulbp2 bumo1  Anti Ulbp2 Bumo1, supplied by Enzo Biochem, 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/antiulbp2/anti+ulbp2+bumo1/pmc03280271-67-13-21 Average 90 stars, based on 1 article reviews
anti-ulbp2 bumo1 - by Bioz Stars,
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Becton Dickinson
anti-ulbp2 Anti Ulbp2, supplied by Becton Dickinson, 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/antiulbp2/anti+ulbp2/pm20154204-47-29-13 Average 90 stars, based on 1 article reviews
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2026-09
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Bio-Techne corporation
human ulbp-2/5/6 antibody Human Ulbp 2/5/6 Antibody, supplied by Bio-Techne corporation, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more https://www.bioz.com/product/antiulbp2/Human+ULBP-2%2F5%2F6+Antibody/bio-techne+corporation___af1298 Average 94 stars, based on 1 article reviews
human ulbp-2/5/6 antibody - by Bioz Stars,
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Amgen
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This gene encodes a major histocompatibility complex (MHC) class I-related molecule that binds to the NKG2D receptor on natural killer (NK) cells to trigger release of multiple cytokines and chemokines that in turn contribute to
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Rabbit anti-Human ULBP2 Polyclonal Antibody
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Ligand for the NKG2D receptor, together with at least ULBP1 and ULBP3. ULBPs activate multiple signaling pathways in primary NK cells, resulting in the production of cytokines and chemokines. Binding of ULBPs ligands to NKG2D
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Ligand for the NKG2D receptor, together with at least ULBP1 and ULBP3. ULBPs activate multiple signaling pathways in primary NK cells, resulting in the production of cytokines and chemokines. Binding of ULBPs ligands to NKG2D
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Image Search Results
Journal: PLoS ONE
Article Title: Redirecting T Cells to Ewing's Sarcoma Family of Tumors by a Chimeric NKG2D Receptor Expressed by Lentiviral Transduction or mRNA Transfection
doi: 10.1371/journal.pone.0031210
Figure Lengend Snippet: The histograms show the surface expression of the respective NKG2D-Ls recognized by specific monoclonal antibodies and analyzed by flow cytometry (filled histograms = specific antibodies; open histograms = isotype controls). The two stably transfected murine B cell lines (Ba/F3) expressing either human MICA or ULBP2 are displayed for comparison.
Article Snippet: NKG2D-Ls were analyzed with anti-MICA (clone AMO1), anti-MICB (clone BMO2), anti-ULBP1 (clone AUMO2),
Techniques: Expressing, Flow Cytometry, Stable Transfection, Transfection
Journal: PLoS ONE
Article Title: Redirecting T Cells to Ewing's Sarcoma Family of Tumors by a Chimeric NKG2D Receptor Expressed by Lentiviral Transduction or mRNA Transfection
doi: 10.1371/journal.pone.0031210
Figure Lengend Snippet: A, antigen-specific enrichment of lentivirally transduced chNKG2D pos MNCs. On day 13 after transduction the cells were co-cultured either with Ba/F3, ULBP2 pos Ba/F3 or without target cells. FACS analysis was performed 6 days later (open histogram, bold line: co-culture with the ULBP2 pos Ba/F3, 86.7% chNKG2D pos T cells; filled histogram, dotted line: co-culture with Ba/F3, 60.7% chNKG2D pos T cells; thin line: cells cultured without target cells, 54.1% chNKG2D pos T cells; open histogram, dotted line = secondary antibody only). B, cytokine production. The diagram shows TNF secretion of purified CD4 pos T cells lentivirally transduced with either chNKG2D (enriched to 83–92% positive cells) or a similar chimeric CMV-specific control receptor (enriched to 69–81%) in response to the indicated cell lines or only medium as control (measured by ELISA; mean of duplicates). Ba/F3 or ULBP2 pos Ba/F3 cells were used for negative and positive control. Statistical significance was calculated for the effects of T cells expressing the chNKG2D versus T cells expressing the control receptor. C, Comparison of the cytotoxic response triggered by chNKG2D either stably or transiently transferred. CD8 pos T cells either unmodified (“without chNKG2D”) or expressing chNKG2D by lentiviral transduction (“LV”; enriched for chNKG2D pos >90%) or mRNA transfection (“mRNA”; 20 hours after electroporation) were co-cultured with dye-labeled murine Ba/F3 cells expressing human ULBP2 (ULBP2-Ba/F3) or not (CTRL-Ba/F3). The diagram shows the percentage of Annexin V pos Ba/F3 target cells after 4 hours of co-culture at the indicated E∶T ratios (mean ± S.D. of triplicates).
Article Snippet: NKG2D-Ls were analyzed with anti-MICA (clone AMO1), anti-MICB (clone BMO2), anti-ULBP1 (clone AUMO2),
Techniques: Transduction, Cell Culture, Co-Culture Assay, Purification, Enzyme-linked Immunosorbent Assay, Positive Control, Expressing, Stable Transfection, Transfection, Electroporation, Labeling