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anti glutamate cysteine ligase catalytic subunit  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology anti glutamate cysteine ligase catalytic subunit
    Anti Glutamate Cysteine Ligase Catalytic Subunit, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 74 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/1663/%CE%B3-GCSc+Antibody/pmc04782222-50-47-53
    Average 94 stars, based on 74 article reviews
    anti glutamate cysteine ligase catalytic subunit - by Bioz Stars, 2026-09
    94/100 stars

    Images

    Related Articles

    Staining:

    Article Title: Lymph node environment drives FSP1 targetability in metastasizing melanoma
    Article Snippet: A TMA containing primary cutaneous melanoma and LN metastases (ME551; TissueArray.com) was used to assess the expression of GCLC, GPX4 and FSP1. .. The sections were stained with antibodies against GPX4 (Abcam, ab125066, 1:500), GCLC (Santa Cruz, sc-390811, 1:500) and FSP1 (Proteintech, 68049-1-Ig, 1:500) using the Zytomed Permanent AP Red Kit (ZUC001-125) according to the manufacturer’s instructions, followed by counterstaining with haematoxylin. .. The slides were scanned with an Axio Scan.Z1 slide scanner (Zeiss).

    Article Title: Lymph node environment drives FSP1 targetability in metastasizing melanoma.
    Article Snippet: A TMA containing primary cutaneous melanoma and LN metastases (ME551; TissueArray.com) was used to assess the expression of GCLC, GPX4 and FSP1. .. The sections were stained with antibodies against GPX4 (Abcam, ab125066, 1:500), GCLC (Santa Cruz, sc-390811, 1:500) and FSP1 (Proteintech, 68049-1-Ig, 1:500) using the Zytomed Permanent AP Red Kit (ZUC001-125) according to the manufacturer’s instructions, followed by counterstaining with haematoxylin. .. Human melanoma cell lines MeWo, SK-MEL-5, A375, murine melanoma lines Yale University Melanoma Model (YUMM) 3.3 and YUMM 5.2, and HEK293T cells were purchased from ATCC.

    other:

    Article Title: Systematic Evaluation Defines the Limits of Ferroptosis in Cancer Therapy
    Article Snippet: TXNRD1 (SC-28321), GCLC (SC-166345) from Santa Cruz Goat Anti-mouse IgG (H+L), HRP (Invitrogen; 62-6520) Goat Anti-rabbit IgG (H+L), HRP (Invitrogen; 31460).

    Incubation:

    Article Title: Arachidonic acid protects against diabetes-induced atrial fibrillation
    Article Snippet: Proteins were transferred to PVDF membranes (FL00010, Millipore, Massachusetts, USA), which were then blocked with 5% non-fat milk for 1 h at room temperature to prevent nonspecific binding. .. Membranes were incubated overnight at 4 °C with primary antibodies against target proteins, followed by incubation with the appropriate HRP-conjugated secondary antibodies at room temperature for 1 h. Protein bands were visualized and quantified using Image Lab software (Bio-Rad Laboratories, USA). β-actin was used as the loading control. ( β-actin (1:2000), AC004, ABclonal, Wuhan, China; γ-GCS (1:500), sc-390811, Santa Cruz Biotechnology, Texas, USA; Nrf2 (1:1000 A21176, ABclonal, Wuhan, China; NPPA (1:1000), ab225844, abcam, Cambridge, UK; Mn-SOD/SOD2 (1:1000), ab68155, abcam, Cambridge, UK; Catalase (CAT) (1:1000), #8841, Cell Signaling Technology, Massachusetts, USA; COL1A1(1:1000), A1352, ABclonal, Wuhan, China; COL3A1(1:1000), A3795, ABclonal, Wuhan, China; IL-1β (1:500), A16288, ABclonal, Wuhan, China; IL-6 (1:500), A0286, ABclonal, Wuhan, China; TNF-α (1:500), A11534, ABclonal, Wuhan, China; Goat Anti-Rabbit IgG H&L (HRP) (1:1000-1:2000), ab6721, abcam, Cambridge, UK; Goat Anti-Mouse IgG H&L (HRP) (1:1000-1:2000),ab6789, abcam, Cambridge, UK.) ..

    Article Title: Arachidonic acid protects against diabetes-induced atrial fibrillation.
    Article Snippet: Proteins were transferred 434 to PVDF membranes (FL00010, Millipore, Massachusetts, USA), 435 which were then blocked with 5% non-fat milk for 1 h at room 436 temperature to prevent nonspecific binding. .. Membranes were 437 incubated overnight at 4 °C with primary antibodies against target 438 proteins, followed by incubation with the appropriate HRP- AR TIC LE IN PR ES S 22 / 67 439 conjugated secondary antibodies at room temperature for 1 h. 440 Protein bands were visualized and quantified using Image Lab 441 software (Bio-Rad Laboratories, USA). β-actin was used as the 442 loading control. ( β-actin (1:2000), AC004, ABclonal, Wuhan, China; 443 γ-GCS (1:500), sc-390811, Santa Cruz Biotechnology, Texas, USA; 444 Nrf2 (1:1000 A21176, ABclonal, Wuhan, China; NPPA (1:1000), 445 ab225844, abcam, Cambridge, UK; Mn-SOD/SOD2 (1:1000), 446 ab68155, abcam, Cambridge, UK; Catalase (CAT) (1:1000), #8841, 447 Cell Signaling Technology, Massachusetts, USA; COL1A1(1:1000), 448 A1352, ABclonal, Wuhan, China; COL3A1(1:1000), A3795, ABclonal, 449 Wuhan, China; IL-1β (1:500), A16288, ABclonal, Wuhan, China; IL-6 450 (1:500) , A0286, ABclonal, Wuhan, China; TNF-α (1:500), A11534, 451 ABclonal, Wuhan, China; Goat Anti-Rabbit IgG H&L (HRP) (1:1000- 452 1:2000), ab6721, abcam, Cambridge, UK; Goat Anti-Mouse IgG H&L 453 (HRP) (1:1000-1:2000),ab6789, abcam, Cambridge, UK.) ..

    Software:

    Article Title: Arachidonic acid protects against diabetes-induced atrial fibrillation
    Article Snippet: Proteins were transferred to PVDF membranes (FL00010, Millipore, Massachusetts, USA), which were then blocked with 5% non-fat milk for 1 h at room temperature to prevent nonspecific binding. .. Membranes were incubated overnight at 4 °C with primary antibodies against target proteins, followed by incubation with the appropriate HRP-conjugated secondary antibodies at room temperature for 1 h. Protein bands were visualized and quantified using Image Lab software (Bio-Rad Laboratories, USA). β-actin was used as the loading control. ( β-actin (1:2000), AC004, ABclonal, Wuhan, China; γ-GCS (1:500), sc-390811, Santa Cruz Biotechnology, Texas, USA; Nrf2 (1:1000 A21176, ABclonal, Wuhan, China; NPPA (1:1000), ab225844, abcam, Cambridge, UK; Mn-SOD/SOD2 (1:1000), ab68155, abcam, Cambridge, UK; Catalase (CAT) (1:1000), #8841, Cell Signaling Technology, Massachusetts, USA; COL1A1(1:1000), A1352, ABclonal, Wuhan, China; COL3A1(1:1000), A3795, ABclonal, Wuhan, China; IL-1β (1:500), A16288, ABclonal, Wuhan, China; IL-6 (1:500), A0286, ABclonal, Wuhan, China; TNF-α (1:500), A11534, ABclonal, Wuhan, China; Goat Anti-Rabbit IgG H&L (HRP) (1:1000-1:2000), ab6721, abcam, Cambridge, UK; Goat Anti-Mouse IgG H&L (HRP) (1:1000-1:2000),ab6789, abcam, Cambridge, UK.) ..

    Article Title: Arachidonic acid protects against diabetes-induced atrial fibrillation.
    Article Snippet: Proteins were transferred 434 to PVDF membranes (FL00010, Millipore, Massachusetts, USA), 435 which were then blocked with 5% non-fat milk for 1 h at room 436 temperature to prevent nonspecific binding. .. Membranes were 437 incubated overnight at 4 °C with primary antibodies against target 438 proteins, followed by incubation with the appropriate HRP- AR TIC LE IN PR ES S 22 / 67 439 conjugated secondary antibodies at room temperature for 1 h. 440 Protein bands were visualized and quantified using Image Lab 441 software (Bio-Rad Laboratories, USA). β-actin was used as the 442 loading control. ( β-actin (1:2000), AC004, ABclonal, Wuhan, China; 443 γ-GCS (1:500), sc-390811, Santa Cruz Biotechnology, Texas, USA; 444 Nrf2 (1:1000 A21176, ABclonal, Wuhan, China; NPPA (1:1000), 445 ab225844, abcam, Cambridge, UK; Mn-SOD/SOD2 (1:1000), 446 ab68155, abcam, Cambridge, UK; Catalase (CAT) (1:1000), #8841, 447 Cell Signaling Technology, Massachusetts, USA; COL1A1(1:1000), 448 A1352, ABclonal, Wuhan, China; COL3A1(1:1000), A3795, ABclonal, 449 Wuhan, China; IL-1β (1:500), A16288, ABclonal, Wuhan, China; IL-6 450 (1:500) , A0286, ABclonal, Wuhan, China; TNF-α (1:500), A11534, 451 ABclonal, Wuhan, China; Goat Anti-Rabbit IgG H&L (HRP) (1:1000- 452 1:2000), ab6721, abcam, Cambridge, UK; Goat Anti-Mouse IgG H&L 453 (HRP) (1:1000-1:2000),ab6789, abcam, Cambridge, UK.) ..

    Control:

    Article Title: Arachidonic acid protects against diabetes-induced atrial fibrillation
    Article Snippet: Proteins were transferred to PVDF membranes (FL00010, Millipore, Massachusetts, USA), which were then blocked with 5% non-fat milk for 1 h at room temperature to prevent nonspecific binding. .. Membranes were incubated overnight at 4 °C with primary antibodies against target proteins, followed by incubation with the appropriate HRP-conjugated secondary antibodies at room temperature for 1 h. Protein bands were visualized and quantified using Image Lab software (Bio-Rad Laboratories, USA). β-actin was used as the loading control. ( β-actin (1:2000), AC004, ABclonal, Wuhan, China; γ-GCS (1:500), sc-390811, Santa Cruz Biotechnology, Texas, USA; Nrf2 (1:1000 A21176, ABclonal, Wuhan, China; NPPA (1:1000), ab225844, abcam, Cambridge, UK; Mn-SOD/SOD2 (1:1000), ab68155, abcam, Cambridge, UK; Catalase (CAT) (1:1000), #8841, Cell Signaling Technology, Massachusetts, USA; COL1A1(1:1000), A1352, ABclonal, Wuhan, China; COL3A1(1:1000), A3795, ABclonal, Wuhan, China; IL-1β (1:500), A16288, ABclonal, Wuhan, China; IL-6 (1:500), A0286, ABclonal, Wuhan, China; TNF-α (1:500), A11534, ABclonal, Wuhan, China; Goat Anti-Rabbit IgG H&L (HRP) (1:1000-1:2000), ab6721, abcam, Cambridge, UK; Goat Anti-Mouse IgG H&L (HRP) (1:1000-1:2000),ab6789, abcam, Cambridge, UK.) ..

    Article Title: Arachidonic acid protects against diabetes-induced atrial fibrillation.
    Article Snippet: Proteins were transferred 434 to PVDF membranes (FL00010, Millipore, Massachusetts, USA), 435 which were then blocked with 5% non-fat milk for 1 h at room 436 temperature to prevent nonspecific binding. .. Membranes were 437 incubated overnight at 4 °C with primary antibodies against target 438 proteins, followed by incubation with the appropriate HRP- AR TIC LE IN PR ES S 22 / 67 439 conjugated secondary antibodies at room temperature for 1 h. 440 Protein bands were visualized and quantified using Image Lab 441 software (Bio-Rad Laboratories, USA). β-actin was used as the 442 loading control. ( β-actin (1:2000), AC004, ABclonal, Wuhan, China; 443 γ-GCS (1:500), sc-390811, Santa Cruz Biotechnology, Texas, USA; 444 Nrf2 (1:1000 A21176, ABclonal, Wuhan, China; NPPA (1:1000), 445 ab225844, abcam, Cambridge, UK; Mn-SOD/SOD2 (1:1000), 446 ab68155, abcam, Cambridge, UK; Catalase (CAT) (1:1000), #8841, 447 Cell Signaling Technology, Massachusetts, USA; COL1A1(1:1000), 448 A1352, ABclonal, Wuhan, China; COL3A1(1:1000), A3795, ABclonal, 449 Wuhan, China; IL-1β (1:500), A16288, ABclonal, Wuhan, China; IL-6 450 (1:500) , A0286, ABclonal, Wuhan, China; TNF-α (1:500), A11534, 451 ABclonal, Wuhan, China; Goat Anti-Rabbit IgG H&L (HRP) (1:1000- 452 1:2000), ab6721, abcam, Cambridge, UK; Goat Anti-Mouse IgG H&L 453 (HRP) (1:1000-1:2000),ab6789, abcam, Cambridge, UK.) ..

    Western Blot:

    Article Title: p75NTR Modulation by LM11A-31 Counteracts Oxidative Stress and Cholesterol Dysmetabolism in a Rotenone-Induced Cell Model of Parkinson’s Disease
    Article Snippet: α-synuclein , sc-12,767 , SantaCruz Biotechnology , IF 1:50. .. γ-GCL , sc-390,811 , SantaCruz Biotechnology , WB 1:500. ..



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    Image Search Results


    SUP physically interacts with TPL through its EAR motif (DLELRL). ( A ) Yeast two-hybrid assays testing interaction between TPL [fused to the GAL4 DNA-binding domain (DBD)] and wild-type SUP (DLELRL), mSUP (DLE A R A ) or mSUP (DLE G R G ) [each fused to the GAL4 activation domain (AD)]. Growth on selection (right panel) detects a physical interaction between TPL and wild-type SUP (DLELRL) only. ( B ) In vitro pull-down assays using GST-tagged N-TPL show a strong interaction with SBP-tagged wild-type SUP (DLELRL) that is weakened by mutation of the EAR motif in SUP (DLE A R A ). Ponceau S staining shows efficient GST protein expression. Full-length blots and quantification of Western blot signal intensities are presented in Supplementary Fig. S3

    Journal: BMC Plant Biology

    Article Title: SUPERMAN requires its EAR motif to recruit the corepressor TOPLESS and to function as a cadastral regulator in floral patterning

    doi: 10.1186/s12870-025-07553-z

    Figure Lengend Snippet: SUP physically interacts with TPL through its EAR motif (DLELRL). ( A ) Yeast two-hybrid assays testing interaction between TPL [fused to the GAL4 DNA-binding domain (DBD)] and wild-type SUP (DLELRL), mSUP (DLE A R A ) or mSUP (DLE G R G ) [each fused to the GAL4 activation domain (AD)]. Growth on selection (right panel) detects a physical interaction between TPL and wild-type SUP (DLELRL) only. ( B ) In vitro pull-down assays using GST-tagged N-TPL show a strong interaction with SBP-tagged wild-type SUP (DLELRL) that is weakened by mutation of the EAR motif in SUP (DLE A R A ). Ponceau S staining shows efficient GST protein expression. Full-length blots and quantification of Western blot signal intensities are presented in Supplementary Fig. S3

    Article Snippet: To verify yeast protein expression, Western blots were stained with 0.1% Ponceau S in 5% v/v acetic acid, washed in water, and analyzed using anti-GAL4 DBD (sc-577) or anti-GAL4 AD (sc-1663) antibodies (Santa Cruz Biotechnologies, Dallas, TX, USA).

    Techniques: Binding Assay, Activation Assay, Selection, In Vitro, Mutagenesis, Staining, Expressing, Western Blot

    CRISPR-generated EAR mutations disrupt physical interaction between SUP and TPL. ( A ) Yeast two-hybrid assays testing interaction between TPL [fused to the GAL4 DNA-binding domain (DBD)] and wild-type SUP (DLELRL), mSUP (DLELL) or mSUP (∆EAR) [each fused to the GAL4 activation domain (AD)]. Growth on selection (right panel) indicates physical interaction between TPL and wild-type SUP (DLELRL) only. ( B ) In vitro pull-down assays using GST-tagged N-TPL show a strong interaction with SBP-tagged wild-type SUP (DLELRL) which is weakened by mutation of the EAR motif in CRISPR allele mSUP (DLELL). Ponceau S staining shows efficient GST protein expression. Full-length blots and quantification of Western blot signal intensities are presented in Supplementary Fig. S7

    Journal: BMC Plant Biology

    Article Title: SUPERMAN requires its EAR motif to recruit the corepressor TOPLESS and to function as a cadastral regulator in floral patterning

    doi: 10.1186/s12870-025-07553-z

    Figure Lengend Snippet: CRISPR-generated EAR mutations disrupt physical interaction between SUP and TPL. ( A ) Yeast two-hybrid assays testing interaction between TPL [fused to the GAL4 DNA-binding domain (DBD)] and wild-type SUP (DLELRL), mSUP (DLELL) or mSUP (∆EAR) [each fused to the GAL4 activation domain (AD)]. Growth on selection (right panel) indicates physical interaction between TPL and wild-type SUP (DLELRL) only. ( B ) In vitro pull-down assays using GST-tagged N-TPL show a strong interaction with SBP-tagged wild-type SUP (DLELRL) which is weakened by mutation of the EAR motif in CRISPR allele mSUP (DLELL). Ponceau S staining shows efficient GST protein expression. Full-length blots and quantification of Western blot signal intensities are presented in Supplementary Fig. S7

    Article Snippet: To verify yeast protein expression, Western blots were stained with 0.1% Ponceau S in 5% v/v acetic acid, washed in water, and analyzed using anti-GAL4 DBD (sc-577) or anti-GAL4 AD (sc-1663) antibodies (Santa Cruz Biotechnologies, Dallas, TX, USA).

    Techniques: CRISPR, Generated, Binding Assay, Activation Assay, Selection, In Vitro, Mutagenesis, Staining, Expressing, Western Blot

    Journal: Cell reports

    Article Title: LHP1 and INO80 cooperate with ethylene signaling for warm ambient temperature response by activating specific bivalent genes

    doi: 10.1016/j.celrep.2024.114758

    Figure Lengend Snippet:

    Article Snippet: Mouse monoclonal GAL4-TA Antibody , Santa Cruz Biotechnology , Cat# sc-46680; RRID: AB_669109.

    Techniques: Virus, Recombinant, Software