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gcl catalytic subunit  (Novus Biologicals)


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    Novus Biologicals gcl catalytic subunit
    Gcl Catalytic Subunit, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 90/100, based on 2 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/gcl+catalytic+subunit+gclc/GCLC+Antibody+(OTI1A3)/10__7554_slash_elife__68590-437-29-33
    Average 90 stars, based on 2 article reviews
    gcl catalytic subunit - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: A novel compound VSC2 has anti-inflammatory and antioxidant properties in microglia and in Parkinson's disease animal model
    Article Snippet: Primary antibodies used were: rabbit polyclonal anti-mouse Nrf2, GCL catalytic subunit (GCLC) (Novus Biologicals, Littleton, CO, USA), GCL modulatory subunit (GCLM), NF-κB and Iba-1 (Wako Chemicals, Osaka, Japan) antibodies; goat polyclonal anti-mouse COX-2, lamin B (Santa Cruz Biotechnology, Santa Cruz, CA, USA), HO-1 (Enzo Life Sciences, Farmingdale, NY, USA), Hsp90 (Cell Signaling, Danvers, MA, USA) and NQO1 (Ab Frontier, Seoul, South Korea) antibodies; and mouse monoclonal anti-mouse β-actin and tyrosine hydroxylase (TH) antibodies (Sigma-Aldrich).

    Immunofluorescence:

    Article Title: A Novel Compound ITC-3 Activates the Nrf2 Signaling and Provides Neuroprotection in Parkinson's Disease Models.
    Article Snippet: Parkinson’s disease (PD) is a progressive neurodegenerative disorder accompanied by a selective loss of the dopamine(DA)ergic neurons residing in the substantia nigra.. There is ample evidence that neuroinflammation and oxidative stress are involved in the pathogenesis of PD.. In the present study, we aimed at protecting the DAergic neurons by suppressing these cellular events and generated a novel synthetic isothiocyanate ITC-3.



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    After 5 days of pre-treatment with placebo (pla, n = 12) or probiotics (pro, n = 12), rats were subjected to acute pancreatitis (AP, n = 12), a sham-procedure (n = 12) or not operated (control, n = 5). Six hours after induction of the AP or sham-procedure, tissue cysteine availability (A) and mucosal glutamate-cysteine-ligase (GCL) activity (B) were determined in ileum samples. (C) RT-PCR was conducted on ileal mRNA. PCR products of specific primers for the catalytic (GCLc, 65 bp) and the modulatory (GCLm, 81 bp) subunit of GCL and for 18S rRNA (65 bp) as control were identified on 2.5% agarose gel, using a GeneRuler 50 bp DNA Ladder (Fermentas GMBH, St. Leon-Rot, Germany). mRNA expression of (D) GCLc and (E) GCLm were quantified. Data are normalized to 18S rRNA expression and expressed as ratio to control animals. The graphs show average (±SD). All analyses were run in triplicates. Comparisons were performed using ANOVA followed by Tukey's HSD.

    Journal: PLoS ONE

    Article Title: Probiotics Prevent Intestinal Barrier Dysfunction in Acute Pancreatitis in Rats via Induction of Ileal Mucosal Glutathione Biosynthesis

    doi: 10.1371/journal.pone.0004512

    Figure Lengend Snippet: After 5 days of pre-treatment with placebo (pla, n = 12) or probiotics (pro, n = 12), rats were subjected to acute pancreatitis (AP, n = 12), a sham-procedure (n = 12) or not operated (control, n = 5). Six hours after induction of the AP or sham-procedure, tissue cysteine availability (A) and mucosal glutamate-cysteine-ligase (GCL) activity (B) were determined in ileum samples. (C) RT-PCR was conducted on ileal mRNA. PCR products of specific primers for the catalytic (GCLc, 65 bp) and the modulatory (GCLm, 81 bp) subunit of GCL and for 18S rRNA (65 bp) as control were identified on 2.5% agarose gel, using a GeneRuler 50 bp DNA Ladder (Fermentas GMBH, St. Leon-Rot, Germany). mRNA expression of (D) GCLc and (E) GCLm were quantified. Data are normalized to 18S rRNA expression and expressed as ratio to control animals. The graphs show average (±SD). All analyses were run in triplicates. Comparisons were performed using ANOVA followed by Tukey's HSD.

    Article Snippet: RT-PCR with mRNA-specific primers for the catalytic (GCLC) and modifier (GCLM) subunits of GCL and 18S rRNA as a reference gene was performed (GCLC-forward 5′-ggcgatgttcttgaaactctg-3′ , GCLC-reverse 5′-cagagggttgggtggttg-3′ ; GCLM-forward 5′-ctgactcacaatgacccaaaag-3′ , GCLM-reverse 5′-ttcaatgtcagggatgctttc-3′ ; 18S rRNA-forward 5′-aatcagttatggttcctttgtcg-3′ , 18S rRNA-reverse 5′-gctctagaattaccacagttatccaa-3′ ; Sigma-Aldrich) and mRNA levels were quantified using SYBR Green based detection.

    Techniques: Activity Assay, Reverse Transcription Polymerase Chain Reaction, Agarose Gel Electrophoresis, Expressing