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recombinant human scd40  (Thermo Fisher)


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    Structured Review

    Thermo Fisher recombinant human scd40

    Recombinant Human Scd40, supplied by Thermo Fisher, 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/recombinant+human+scd40/pmc11615188-345-19-21
    Average 90 stars, based on 1 article reviews
    recombinant human scd40 - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "PI3K-dependent reprogramming of hexokinase isoforms controls glucose metabolism and functional responses of B lymphocytes"

    Article Title: PI3K-dependent reprogramming of hexokinase isoforms controls glucose metabolism and functional responses of B lymphocytes

    Journal: iScience

    doi: 10.1016/j.isci.2024.110939


    Figure Legend Snippet:

    Techniques Used: Activation Assay, Marker, Recombinant, Staining, Cell Isolation, Software

    Related Articles

    Cell Stimulation:

    Article Title: PI3K-dependent reprogramming of hexokinase isoforms controls glucose metabolism and functional responses of B lymphocytes
    Article Snippet: Where indicated, cells were stimulated with 2 μg/mL of anti-CD40 (BD Biosciences, #553721), 10 ng/mL of IL4 (Peprotech, #214-14-20UG) and 10 μg/mL of anti-IgM (Jackson ImmunoResearch Laboratories, #115-006-020). .. Human B cell stimulation used 10 ng/mL Goat F(ab’) 2 Anti-human IgM (Southern Biotech #2022-01), 2 ug/mL of recombinant human sCD40 (invitrogen PHP0025), and 10 ng/mL of recombinant human IL-4 (R&D systems, #204-IL/CF). .. Inhibitors used were the PI3Kdelta inhibitor Idelalisib, pan-PI3K inhibitor Pictilisib, Akt inhibitors Ipatasertib or MK-2206, mTOR inhibitors rapamycin, Sapanisertib or JR-AB2-01 or glutaminase inhibitor Telaglenastat (all from Selleck Chemicals).

    Recombinant:

    Article Title: PI3K-dependent reprogramming of hexokinase isoforms controls glucose metabolism and functional responses of B lymphocytes
    Article Snippet: Where indicated, cells were stimulated with 2 μg/mL of anti-CD40 (BD Biosciences, #553721), 10 ng/mL of IL4 (Peprotech, #214-14-20UG) and 10 μg/mL of anti-IgM (Jackson ImmunoResearch Laboratories, #115-006-020). .. Human B cell stimulation used 10 ng/mL Goat F(ab’) 2 Anti-human IgM (Southern Biotech #2022-01), 2 ug/mL of recombinant human sCD40 (invitrogen PHP0025), and 10 ng/mL of recombinant human IL-4 (R&D systems, #204-IL/CF). .. Inhibitors used were the PI3Kdelta inhibitor Idelalisib, pan-PI3K inhibitor Pictilisib, Akt inhibitors Ipatasertib or MK-2206, mTOR inhibitors rapamycin, Sapanisertib or JR-AB2-01 or glutaminase inhibitor Telaglenastat (all from Selleck Chemicals).



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    PeproTech recombinant human scd40 ligand (scd40l; 310-02)
    a Diverse stimulants abrogate venetoclax cytotoxicity against patient-derived CLL cells. Primary cells (1 × 10 6 cells/mL) obtained from nine patients with CLL were treated with 0.1% DMSO (vehicle control), and 1 nM venetoclax alone and in combination with 100 ng/mL IFNγ, 10 nM PMA/1 µM ionomycin, and 100 ng/mL <t>sCD40L</t> for 24 h. The metabolic activities of the cells were determined using the PrestoBlue assay. Data are means ± SEM of ≥ three independent experiments, each carried out in duplicate. Two-way ANOVA (post hoc Tukey); *, **, and **** denote p < 0.05, p < 0.01, and p < 0.0001, respectively; b Cytoprotective effects of IFNγ in the patient-derived CLL cells undergoing spontaneous and venetoclax-induced apoptosis. CLL cells (1 × 10 6 cells/mL) were treated with 0.1% DMSO (vehicle control) and 1 nM venetoclax, 100 ng/mL IFNγ, and their combination for 24 h. Apoptosis was assessed using the SYTOX Blue/annexin V assay. Representative dot plots (left) and means ± SEM of three independent experiments (right) are shown. Two-way ANOVA (post hoc Tukey); *, **, ***, and **** denote p < 0.05, p < 0.01, p < 0.001, and p < 0.0001, respectively; c Nuclear translocation of NFκB in the primary CLL cells. CLL cells (1 × 10 6 c ells/mL) from three patients with CLL were treated with 0.1% DMSO (vehicle control), 100 ng/mL IFNγ, 10 nM PMA/1 µM ionomycin, and 100 ng/mL sCD40L for 1 h. Quantification (left) and representative images (right) are shown for the translocation of NFκB to the nucleus, using imaging flow cytometry. One-way ANOVA (post hoc Dunnett); **** denotes p < 0.0001.
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    Average 90 stars, based on 1 article reviews
    recombinant human scd40 ligand (scd40l; 310-02) - by Bioz Stars, 2026-09
    90/100 stars
      Buy from Supplier

    Image Search Results


    Journal: iScience

    Article Title: PI3K-dependent reprogramming of hexokinase isoforms controls glucose metabolism and functional responses of B lymphocytes

    doi: 10.1016/j.isci.2024.110939

    Figure Lengend Snippet:

    Article Snippet: Human B cell stimulation used 10 ng/mL Goat F(ab’) 2 Anti-human IgM (Southern Biotech #2022-01), 2 ug/mL of recombinant human sCD40 (invitrogen PHP0025), and 10 ng/mL of recombinant human IL-4 (R&D systems, #204-IL/CF).

    Techniques: Activation Assay, Marker, Recombinant, Staining, Cell Isolation, Software

    a Diverse stimulants abrogate venetoclax cytotoxicity against patient-derived CLL cells. Primary cells (1 × 10 6 cells/mL) obtained from nine patients with CLL were treated with 0.1% DMSO (vehicle control), and 1 nM venetoclax alone and in combination with 100 ng/mL IFNγ, 10 nM PMA/1 µM ionomycin, and 100 ng/mL sCD40L for 24 h. The metabolic activities of the cells were determined using the PrestoBlue assay. Data are means ± SEM of ≥ three independent experiments, each carried out in duplicate. Two-way ANOVA (post hoc Tukey); *, **, and **** denote p < 0.05, p < 0.01, and p < 0.0001, respectively; b Cytoprotective effects of IFNγ in the patient-derived CLL cells undergoing spontaneous and venetoclax-induced apoptosis. CLL cells (1 × 10 6 cells/mL) were treated with 0.1% DMSO (vehicle control) and 1 nM venetoclax, 100 ng/mL IFNγ, and their combination for 24 h. Apoptosis was assessed using the SYTOX Blue/annexin V assay. Representative dot plots (left) and means ± SEM of three independent experiments (right) are shown. Two-way ANOVA (post hoc Tukey); *, **, ***, and **** denote p < 0.05, p < 0.01, p < 0.001, and p < 0.0001, respectively; c Nuclear translocation of NFκB in the primary CLL cells. CLL cells (1 × 10 6 c ells/mL) from three patients with CLL were treated with 0.1% DMSO (vehicle control), 100 ng/mL IFNγ, 10 nM PMA/1 µM ionomycin, and 100 ng/mL sCD40L for 1 h. Quantification (left) and representative images (right) are shown for the translocation of NFκB to the nucleus, using imaging flow cytometry. One-way ANOVA (post hoc Dunnett); **** denotes p < 0.0001.

    Journal: Cell Death & Disease

    Article Title: Inhibition of p38 MAPK or immunoproteasome overcomes resistance of chronic lymphocytic leukemia cells to Bcl-2 antagonist venetoclax

    doi: 10.1038/s41419-022-05287-6

    Figure Lengend Snippet: a Diverse stimulants abrogate venetoclax cytotoxicity against patient-derived CLL cells. Primary cells (1 × 10 6 cells/mL) obtained from nine patients with CLL were treated with 0.1% DMSO (vehicle control), and 1 nM venetoclax alone and in combination with 100 ng/mL IFNγ, 10 nM PMA/1 µM ionomycin, and 100 ng/mL sCD40L for 24 h. The metabolic activities of the cells were determined using the PrestoBlue assay. Data are means ± SEM of ≥ three independent experiments, each carried out in duplicate. Two-way ANOVA (post hoc Tukey); *, **, and **** denote p < 0.05, p < 0.01, and p < 0.0001, respectively; b Cytoprotective effects of IFNγ in the patient-derived CLL cells undergoing spontaneous and venetoclax-induced apoptosis. CLL cells (1 × 10 6 cells/mL) were treated with 0.1% DMSO (vehicle control) and 1 nM venetoclax, 100 ng/mL IFNγ, and their combination for 24 h. Apoptosis was assessed using the SYTOX Blue/annexin V assay. Representative dot plots (left) and means ± SEM of three independent experiments (right) are shown. Two-way ANOVA (post hoc Tukey); *, **, ***, and **** denote p < 0.05, p < 0.01, p < 0.001, and p < 0.0001, respectively; c Nuclear translocation of NFκB in the primary CLL cells. CLL cells (1 × 10 6 c ells/mL) from three patients with CLL were treated with 0.1% DMSO (vehicle control), 100 ng/mL IFNγ, 10 nM PMA/1 µM ionomycin, and 100 ng/mL sCD40L for 1 h. Quantification (left) and representative images (right) are shown for the translocation of NFκB to the nucleus, using imaging flow cytometry. One-way ANOVA (post hoc Dunnett); **** denotes p < 0.0001.

    Article Snippet: Recombinant human sCD40 ligand (sCD40L; 310-02) was from PeproTech (London, UK).

    Techniques: Derivative Assay, Prestoblue Assay, Annexin V Assay, Translocation Assay, Imaging, Flow Cytometry