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nmol l tumor necrosis factor  (R&D Systems)


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    R&D Systems nmol l tumor necrosis factor
    Nmol L Tumor Necrosis Factor, supplied by R&D Systems, used in various techniques. Bioz Stars score: 97/100, based on 1392 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/recombinant+protein/pmc13054578-103-43-49?v=R%26D+Systems
    Average 97 stars, based on 1392 article reviews
    nmol l tumor necrosis factor - by Bioz Stars, 2026-07
    97/100 stars

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    SDS-PAGE analysis of expression of pET21a-GnRH6-CRM197 in E. coli. BL21. Lane 1, standard molecular weight marker; Lane 2, non-induced recombinant bacteria; Lane 3, recombinant bacteria induced after 12 h.

    Journal: Poultry Science

    Article Title: Immunocastration with recombinant GnRH6-CRM197 fusion protein improves reproductive suppression and meat tenderness in roosters

    doi: 10.1016/j.psj.2026.107046

    Figure Lengend Snippet: SDS-PAGE analysis of expression of pET21a-GnRH6-CRM197 in E. coli. BL21. Lane 1, standard molecular weight marker; Lane 2, non-induced recombinant bacteria; Lane 3, recombinant bacteria induced after 12 h.

    Article Snippet: The GnRH6-CRM197 recombinant protein was separated on a 12.5% SDS polyacrylamide gel at 120 V. It was then transferred to a 0.45μm polyvinylidene fluoride (PVDF) membrane (Pulilai, Beijing, China) at 250 mA for 1 hour using a transfer system (BVT-2, Servicebio, Wuhan, China).

    Techniques: SDS Page, Expressing, Molecular Weight, Marker, Recombinant, Bacteria

    WB analysis of recombinant GnRH6-CRM197 protein. Lane 1, standard molecular weight marker; Lane 2, recombinant GnRH6-CRM197 fusion protein reacted with rabbit polyclonal to GnRH (dilution 1:2000) .

    Journal: Poultry Science

    Article Title: Immunocastration with recombinant GnRH6-CRM197 fusion protein improves reproductive suppression and meat tenderness in roosters

    doi: 10.1016/j.psj.2026.107046

    Figure Lengend Snippet: WB analysis of recombinant GnRH6-CRM197 protein. Lane 1, standard molecular weight marker; Lane 2, recombinant GnRH6-CRM197 fusion protein reacted with rabbit polyclonal to GnRH (dilution 1:2000) .

    Article Snippet: The GnRH6-CRM197 recombinant protein was separated on a 12.5% SDS polyacrylamide gel at 120 V. It was then transferred to a 0.45μm polyvinylidene fluoride (PVDF) membrane (Pulilai, Beijing, China) at 250 mA for 1 hour using a transfer system (BVT-2, Servicebio, Wuhan, China).

    Techniques: Recombinant, Molecular Weight, Marker

    The effect of recombinant anti-GnRH6-CRM197 on serum anti-GnRH antibody of roosters. The arrow refers to the immune time; the first immunity of roosters is 4 W; * P < 0.05; ** P < 0.01 (n = 20 per group).

    Journal: Poultry Science

    Article Title: Immunocastration with recombinant GnRH6-CRM197 fusion protein improves reproductive suppression and meat tenderness in roosters

    doi: 10.1016/j.psj.2026.107046

    Figure Lengend Snippet: The effect of recombinant anti-GnRH6-CRM197 on serum anti-GnRH antibody of roosters. The arrow refers to the immune time; the first immunity of roosters is 4 W; * P < 0.05; ** P < 0.01 (n = 20 per group).

    Article Snippet: The GnRH6-CRM197 recombinant protein was separated on a 12.5% SDS polyacrylamide gel at 120 V. It was then transferred to a 0.45μm polyvinylidene fluoride (PVDF) membrane (Pulilai, Beijing, China) at 250 mA for 1 hour using a transfer system (BVT-2, Servicebio, Wuhan, China).

    Techniques: Recombinant

    The effect of recombinant GnRH6-CRM197 on serum testosterone levels of roosters. * P < 0.05; ** P < 0.01 (n = 20 per group).

    Journal: Poultry Science

    Article Title: Immunocastration with recombinant GnRH6-CRM197 fusion protein improves reproductive suppression and meat tenderness in roosters

    doi: 10.1016/j.psj.2026.107046

    Figure Lengend Snippet: The effect of recombinant GnRH6-CRM197 on serum testosterone levels of roosters. * P < 0.05; ** P < 0.01 (n = 20 per group).

    Article Snippet: The GnRH6-CRM197 recombinant protein was separated on a 12.5% SDS polyacrylamide gel at 120 V. It was then transferred to a 0.45μm polyvinylidene fluoride (PVDF) membrane (Pulilai, Beijing, China) at 250 mA for 1 hour using a transfer system (BVT-2, Servicebio, Wuhan, China).

    Techniques: Recombinant