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its g  (MedChemExpress)


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    Structured Review

    MedChemExpress its g
    Its G, supplied by MedChemExpress, used in various techniques. Bioz Stars score: 94/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/its+g/Insulin-Transferrin-Selenium/pmc13001038-53-42-44
    Average 94 stars, based on 15 article reviews
    its g - by Bioz Stars, 2026-10
    94/100 stars

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    other:

    Article Title: A Ce-MOFs-based melatonin delivery platform for treating hepatic ischemia-reperfusion injury by interrupting the oxidation-inflammation loop
    Article Snippet: AML12 cells were maintained at 37 °C in a humidified incubator with 5% CO2 in DMEM/F12 (Gibco) with 10% FBS, 1% penicillin/streptomycin (Gibco), 0.5% ITS-G (MCE), and 40 ng/mL dexamethasone (MCE).

    Cell Culture:

    Article Title: Granulosa Cell‐Layer Stiffening Prevents Escape of Mural Granulosa Cells from the Post‐Ovulatory Follicle
    Article Snippet: In experiments studying the signaling pathway, Forsklin (MCE, USA) and H‐89 (MCE, USA) dissolved in DMSO were added to the ovulation induction solution at concentrations of 20 and 50 μM, respectively. .. After ovulation, the post‐ovulatory follicles were transferred to luteal culture medium and cultured for up to 24 h. The luteal culture medium consisted of ɑ‐MEM supplemented with ITS‐G (1%), FBS (5%), FSH (10 mIU mL −1 ), hCG (1.5 IU mL −1 ), EGF (10 ng mL −1 ), Prolactin (1 ng mL −1 , MCE, USA), Cholesterol (10 μM) (MCE, USA), and penicillin/streptomycin (100 U mL −1 ). .. To stimulate follicle growth to the pre‐ovulatory stage in weaned juvenile mice, an injection of PMSG (5 IU) (Ningbo Sansheng Biological Technology, China) was administered.

    Article Title: SIRT7 facilitates ferroptosis resistance of melanocytes via activating the SMAD3-ATF3-GPX4 signaling pathway in vitiligo
    Article Snippet: .. They were cultured using HAM’s F10 medium (11550043, Invitrogen, Carlsbad, CA, USA) containing 20 % FBS (A5669401, Invitrogen), 200 nM cholera toxin (C8052, Sigma-Aldrich, St. Louis, MO, USA), 100 μM 3-Isobutyl-1-methylxanthine (IBMX, HY-12318, MedChemExpress, NJ, USA), 100 nM PMA (16561–29-8, MedChemExpress) and ITS-G (41400045, MedChemExpress). ..

    Article Title: SIRT7 facilitates ferroptosis resistance of melanocytes via activating the SMAD3-ATF3-GPX4 signaling pathway in vitiligo.
    Article Snippet: .. They were cultured using HAM’s F10 medium (11550043, Invitrogen, Carlsbad, CA, USA) containing 20 % FBS (A5669401, Invitrogen), 200 nM cholera toxin (C8052, Sigma-Aldrich, St. Louis, MO, USA), 100 lM 3-Isobutyl-1-methylxanthine (IBMX, HY-12318, MedChemExpress, NJ, USA), 100 nM PMA (16561–29-8, MedChemExpress) and ITS-G (41400045, MedChemExpress). ..

    Article Title: Granulosa Cell‐Layer Stiffening Prevents Escape of Mural Granulosa Cells from the Post‐Ovulatory Follicle
    Article Snippet: The culture medium for maturation consisted of ɑ‐MEM (Gibco, USA) supplemented with ITS‐G (1%) (Macklin, China), FBS (5%) (Serana, Germany), FSH (10 mIU mL −1 , NSHF, China), and penicillin/streptomycin (100 U mL −1 , Servicebio, China). .. After 96 h of culture, follicles reaching the pre‐ovulatory stage (500‐550 μm) were transferred to ovulation‐inducing medium and cultured for up to 16 h. The ovulation‐inducing medium contained ɑ‐MEM supplemented with ITS‐G (1%), FBS (5%), FSH (10 mIU mL −1 ), hCG (1.5 IU mL −1 , NSHF, China), EGF (10 ng mL −1 , PeproThec, USA), D‐Glucose (5 mg mL −1 , MCE, USA), and penicillin/streptomycin (100 U mL −1 ). .. In experiments studying the signaling pathway, Forsklin (MCE, USA) and H‐89 (MCE, USA) dissolved in DMSO were added to the ovulation induction solution at concentrations of 20 and 50 μM, respectively.

    Article Title: Granulosa Cell-Layer Stiffening Prevents Escape of Mural Granulosa Cells from the Post-Ovulatory Follicle.
    Article Snippet: In experiments studying the signaling pathway, Forsklin (MCE, USA) and H-89 (MCE, USA) dissolved in DMSO were added to the ovulation induction solution at concentrations of 20 and 50 μM, respectively. .. After ovulation, the post-ovulatory follicles were transferred to luteal culture medium and cultured for up to 24 h. The luteal culture medium consisted of ɑ-MEM supplemented with ITS-G (1%), FBS (5%), FSH (10 mIU mL−1), hCG (1.5 IU mL−1), EGF (10 ng mL−1), Prolactin (1 ng mL−1, MCE, USA), Cholesterol (10 μM) (MCE, USA), and penicillin/streptomycin (100 U mL−1). .. Superovulation: To stimulate follicle growth to the pre-ovulatory stage in weaned juvenile mice, an injection of PMSG (5 IU) (Ningbo Sansheng Biological Technology, China) was administered.

    Incubation:

    Article Title: UGCG promotes chemoresistance and breast cancer progression via NF-κB and Wnt/β-catenin pathway activation.
    Article Snippet: Background: Taxane-based chemotherapy is the primary treatment for triple-negative breast cancer (TNBC), yet clinical outcomes remain unsatisfactory due to the persistence of chemoresistance.. Identifying key factors that contribute to chemoresistance and understanding the associated molecular mechanisms is therefore essential.. Method: The GEO databases were utilized to pinpoint factors related to chemoresistance, which were subsequently validated using clinical tissue samples.

    Article Title: UGCG promotes chemoresistance and breast cancer progression via NF-κB and Wnt/β-catenin pathway activation
    Article Snippet: The ALDH-positive cell population was identified by utilizing a FACSCalibur flow cytometer (BD Biosciences, USA). .. Chopped tissues were incubated at 37 °C for 2 h with the addition of 1% BSA, ITS-G (BasalMedia Technologies Company, China), Primocin (Invitrogen, USA), 5 μM Y-27,632 (MCE, USA), 10 mM HEPES (Thermo, USA), collagenase I and III (Worthington, Italy), and 1000 U/mL hyaluronidase (Sigma-Aldrich, USA). ..



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