recombinant cd80  (BPS Bioscience)

Journal: Scientific reports

Article Title: Identification of m6A methyltransferase-related WTAP and ZC3H13 predicts immune infiltrates in glioblastoma.

doi: 10.1038/s41598-025-88671-4

Figure Lengend Snippet: Fig. 9. Relative expression of genes expression in GBM tissues. Expression levels of WTAP and ZC3H13 genes were compared with those of the control group on GBM tissues, 10 GBM and adjacent tissues, respectively (A). The expression levels of siRNA WTAP and overexpression ZC3H13 genes (B and C). The expression levels of CD27, CD70, CD80, CD86, ICOS, CTLA4, and LAG3 in siRNA WTAP and overexpression ZC3H13 were demonstrated in Fig. 9D and F, respectively. The result were determined by qRT-PCR. The data are mean ± standard deviation of six replicate experiments. * P < 0.05, **P < 0.01 and ***P < 0.001 compared with the corresponding control values.

Article Snippet: After blocking with 5% nonfat milk, the membranes were immunoblotted with the primary antibodies: WTAP (A04296-2, Boster Biotech, Wuhan, China), CD27 (A01148-2, Boster Biotech), CD70 (A02853-2, Boster Biotech), CD80 (A00196-3, Boster Biotech), CD86(BM4121, Boster Biotech), ICOS (A00291-2, Boster Biotech), CTLA4 (A00020-1, Boster Biotech), LAG3 (M02869-2, Boster Biotech), Beta-actin (BM3873, Boster Biotech).

Techniques: Expressing, Control, Over Expression, Quantitative RT-PCR, Standard Deviation

Journal: Advanced Science

Article Title: High‐Affinity Superantigen‐Based Trifunctional Immune Cell Engager Synergizes NK and T Cell Activation for Tumor Suppression

doi: 10.1002/advs.202310204

Figure Lengend Snippet: Identification of SEB variants with enhanced immunoreceptor binding affinity. a) The stepwise illustration of the SEB yeast library establishment. The library was incubated with 1 µ m of recombinant human CD28, and the population exhibiting a higher binding affinity to human CD28 was sorted through flow cytometry. The sorted library was then amplified, resulting in the production of 4 subsequent generations of libraries. b) The binding affinity of all the sorted SEB libraries to mouse and human CD28 as measured by flow cytometry. c) Missense mutations were identified from 9 single clones selected from the S4 SEB yeast library. d) In the SEB structure (pdb: 1sbb), the wild‐type SEB (upper panel) and the 9 mutated amino acids on the S4 clone (SEB #3) (lower panel) are shown in the pink sticks using PyMol. e) Schematic illustration demonstrating the potential hindrance effect of the D55G mutation on TCR interaction and downstream NFAT signaling. f) The binding affinity of all the SEB variants toward the immunoreceptors (CD28, CD80, CD86, and MHC‐II) was tested using flow cytometry. The mean fluorescence of protein binding on the surface‐displayed population is shown.

Article Snippet: For the other immunoreceptors binding affinity tests, induced yeast cells were incubated with 1 µ m human Fc tagged mouse CD28 recombinant protein (SinoBiological, 50103‐M02H), 5 µ m His tagged human CD80 recombinant protein (SinoBiological, 10698‐H08H), 5 µ m His tagged mouse CD80 recombinant protein (SinoBiological, 50446‐M08H), 5 µ m His tagged human CD86 recombinant protein (SinoBiological, 10699‐H08H), 5 µ m His tagged mouse CD86 recombinant protein (SinoBiological, 50068‐M08H), 2 µ m His tagged human HLA‐DRA recombinant protein (Cusabio, CSB‐EP360793HU), 0.5 µ m human Fc tagged human CD2 recombinant protein (SinoBiological, 10982‐H02H), 2 µ m His tagged mouse CD2 recombinant protein (SinoBiological, 50537‐M08H), 0.5 µ m human Fc tagged human CD58 recombinant protein (SinoBiological, 12409‐H02H), and 0.5 µ m human Fc tagged mouse CD48 recombinant protein (SinoBiological, 50415‐M02H) at 4 °C for 2 h. Yeast cells were washed with PBS once and stained with the anti‐human IgG Fc antibody (Abcam, ab131612), the anti‐His tag antibody (Biolegend, 362603), and the anti‐HA tag antibody (Biolegend, 682404) at 4 °C for 30 min.

Techniques: Binding Assay, Incubation, Recombinant, Flow Cytometry, Amplification, Clone Assay, Mutagenesis, Fluorescence, Protein Binding

Journal: Biomimetics

Article Title: Developing a Biomimetic 3D Neointimal Layer as a Prothrombotic Substrate for a Humanized In Vitro Model of Atherothrombosis

doi: 10.3390/biomimetics9060372

Figure Lengend Snippet: Culturing THP-1-derived M1 macrophages within a 3D collagen hydrogel. ( A ) THP-1 cells were mixed at a cell density of 3 × 10 6 cells/mL into a neutralized solution of 3 mg/mL type I collagen. Following setting, the hydrogel was incubated with a supplemented RPMI medium containing 50 nM PMA and then incubated for 48 h at 37 °C, 5% CO 2 . Hydrogels were stained by a live/dead staining solution and imaged by confocal microscopy. ( B ) THP-1 cell suspensions were seeded at 6 × 10 5 cells/hydrogel in RPMI media with 50 nM PMA. Cells were then incubated at 5% CO 2 , 37 °C for 48 h. Cells were rested by incubation in a PMA-free media for 24 h, and then cells were transferred into fresh RPMI containing either ( Top ) 100 ng/mL LPS and 20 ng/mL IFN-γ or ( Bottom ) their vehicle, DMSO for a further 72 h. Collagen hydrogels were then fixed and then immunolabelled using an unconjugated CD80 antibody and a FITC-labelled secondary antibody. Samples were then subjected to z-stack imaging using a confocal microscope. An x-y slice from the confocal slice with the highest mean fluorescence is shown along ( left ) and overlaid over the transmitted light image ( right ) ( C ) Image J analysis of the mean slice FITC fluorescence through the hydrogel. n = 6, * indicates p < 0.05.

Article Snippet: Monoclonal recombinant human full-length CD80 protein antibody was purchased from Novus Biologicals (Abingdon, UK).

Techniques: Derivative Assay, Incubation, Staining, Confocal Microscopy, Imaging, Microscopy, Fluorescence