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anti stat5a  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology anti stat5a
    Anti Stat5a, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 95/100, based on 499 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/stat5a/Stat5a+Antibody/pm41898298-93-0-1
    Average 95 stars, based on 499 article reviews
    anti stat5a - by Bioz Stars, 2026-10
    95/100 stars

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    Related Articles

    Chromatin Immunoprecipitation:

    Article Title: Cell-specific and shared regulatory elements control a multigene locus active in mammary and salivary glands.
    Article Snippet: .. The following antibodies were used for ChIP-seq: STAT5A (Santa Cruz Biotechnology, sc-271542), GR (Thermo Fisher Scientific, PA1-511A), NFIB (Sigma-Aldrich, HPA003956), MED1 (Bethyl Laboratory, A300−793A), H3K27ac (Abcam, ab4729), RNA polymerase II (Abcam, ab5408), H3K4me1 (Active Motif, 39297) and H3K4me3 (Millipore, 07-473). ..

    Article Title: Disease-Associated Mutations of the STAT5B SH2 Domain Regulate Cytokine-Driven Enhancer Function and Mammary Development
    Article Snippet: The chromatin was fragmented to 250–500 bp using sonicator 3000 (30 cycles; 20 s pulse/20 s rest, Misonix Sonicators), checked on DNA gel, and further lysed in RIPA buffer. .. One milligram of total protein was immunoprecipitated with Dynabeads Protein A (Novex) coated with ChIP-seq grade antibodies: STAT5A (Santa Cruz Biotechnology, sc-271542), STAT5B (R&D systems, AF1584; ThermoFisher scientific, 13-5300), NFIB (Sigma-Aldrich, HPA003956), H3K27ac (Abcam, ab4729) and RNA polymerase II (Abcam, ab5408). .. Libraries for next-generation sequencing were prepared with NEBNext Ultra II DNA library prep kit for illumina (New England Biolabs, M0287L) and sequenced with the NovaSeq 6000 instrument (Illumina).

    Article Title: Disease-Associated Mutations of the STAT5B SH2 Domain Regulate Cytokine-Driven Enhancer Function and Mammary Development.
    Article Snippet: The chromatin was fragmented to 250–500 bp using sonicator 3000 (30 cycles; 20 s pulse/20 s rest, Misonix Sonicators), checked on DNA gel, and further lysed in RIPA buffer. .. One milligram of total protein was immunoprecipitated with Dynabeads Protein A (Novex) coated with ChIP-seq grade antibodies: STAT5A (Santa Cruz Biotechnology, sc-271542), STAT5B (R&D systems, AF1584; ThermoFisher scientific, 13-5300), NFIB (Sigma-Aldrich, HPA003956), H3K27ac (Abcam, ab4729) and RNA polymerase II (Abcam, ab5408). .. Libraries for next-generation sequencing were prepared with NEBNext Ultra II DNA library prep kit for illumina (New England Biolabs, M0287L) and sequenced with the NovaSeq 6000 instrument (Illumina).

    Article Title: STAT5B leukemic mutations, altering SH2 tyrosine 665, have opposing impacts on immune gene programs
    Article Snippet: .. The following antibodies were used for ChIP-seq: STAT5A (Santa Cruz Biotechnology, sc-271542), STAT5B (R&D systems, AF1584; ThermoFisher scientific, 13-5300), H3K27ac (Abcam, ab4729) and RNA polymerase II (Abcam, ab5408). .. Libraries for next-generation sequencing were prepared and sequenced with the NovaSeq 6000 instrument (Illumina).

    Article Title: STAT5B SH2 variants disrupt mammary enhancers and the stability of genetic programs during pregnancy
    Article Snippet: .. The following antibodies were used for ChIP-seq: STAT5A (Santa Cruz Biotechnology, sc-271542), STAT5B (R&D systems, AF1584; ThermoFisher scientific, 13-5300), H3K27ac (Abcam, ab4729) and RNA polymerase II (Abcam, ab5408). .. Libraries for next-generation sequencing were prepared and sequenced with the NovaSeq 6000 instrument (Illumina).

    Immunoprecipitation:

    Article Title: Disease-Associated Mutations of the STAT5B SH2 Domain Regulate Cytokine-Driven Enhancer Function and Mammary Development
    Article Snippet: The chromatin was fragmented to 250–500 bp using sonicator 3000 (30 cycles; 20 s pulse/20 s rest, Misonix Sonicators), checked on DNA gel, and further lysed in RIPA buffer. .. One milligram of total protein was immunoprecipitated with Dynabeads Protein A (Novex) coated with ChIP-seq grade antibodies: STAT5A (Santa Cruz Biotechnology, sc-271542), STAT5B (R&D systems, AF1584; ThermoFisher scientific, 13-5300), NFIB (Sigma-Aldrich, HPA003956), H3K27ac (Abcam, ab4729) and RNA polymerase II (Abcam, ab5408). .. Libraries for next-generation sequencing were prepared with NEBNext Ultra II DNA library prep kit for illumina (New England Biolabs, M0287L) and sequenced with the NovaSeq 6000 instrument (Illumina).

    Article Title: Disease-Associated Mutations of the STAT5B SH2 Domain Regulate Cytokine-Driven Enhancer Function and Mammary Development.
    Article Snippet: The chromatin was fragmented to 250–500 bp using sonicator 3000 (30 cycles; 20 s pulse/20 s rest, Misonix Sonicators), checked on DNA gel, and further lysed in RIPA buffer. .. One milligram of total protein was immunoprecipitated with Dynabeads Protein A (Novex) coated with ChIP-seq grade antibodies: STAT5A (Santa Cruz Biotechnology, sc-271542), STAT5B (R&D systems, AF1584; ThermoFisher scientific, 13-5300), NFIB (Sigma-Aldrich, HPA003956), H3K27ac (Abcam, ab4729) and RNA polymerase II (Abcam, ab5408). .. Libraries for next-generation sequencing were prepared with NEBNext Ultra II DNA library prep kit for illumina (New England Biolabs, M0287L) and sequenced with the NovaSeq 6000 instrument (Illumina).

    Expressing:

    Article Title: Disease-Associated Mutations of the STAT5B SH2 Domain Regulate Cytokine-Driven Enhancer Function and Mammary Development
    Article Snippet: Antigen retrieval was performed by boiling the slides in Antigen Unmasking Solution (Vector Laboratories) for 10 min. Endogenous peroxidase activity was quenched by incubating the slides in freshly prepared 3% hydrogen peroxide for 10 min. After rinsing in water, non-specific binding was blocked by incubating the slides with 2.5% goat serum (Vector Laboratories) for 1 h at room temperature. .. The expression of STAT5A and STAT5B proteins was detected by overnight incubation with primary antibodies: STAT5A (1:200, Santa Cruz Biotechnology, sc-271542) and STAT5B (1:200, R&D Systems, AF1584) at room temperature. .. The slides were subsequently incubated with the appropriate secondary antibody (Goat anti-mouse or anti-rabbit IgG, Vector Laboratories, MP-7452 and MP-7451) for 1 h. Detection was carried out using the DAB (3,3’-diaminobenzidine) substrate (Vector Laboratories) for 10 min.

    Incubation:

    Article Title: Disease-Associated Mutations of the STAT5B SH2 Domain Regulate Cytokine-Driven Enhancer Function and Mammary Development
    Article Snippet: Antigen retrieval was performed by boiling the slides in Antigen Unmasking Solution (Vector Laboratories) for 10 min. Endogenous peroxidase activity was quenched by incubating the slides in freshly prepared 3% hydrogen peroxide for 10 min. After rinsing in water, non-specific binding was blocked by incubating the slides with 2.5% goat serum (Vector Laboratories) for 1 h at room temperature. .. The expression of STAT5A and STAT5B proteins was detected by overnight incubation with primary antibodies: STAT5A (1:200, Santa Cruz Biotechnology, sc-271542) and STAT5B (1:200, R&D Systems, AF1584) at room temperature. .. The slides were subsequently incubated with the appropriate secondary antibody (Goat anti-mouse or anti-rabbit IgG, Vector Laboratories, MP-7452 and MP-7451) for 1 h. Detection was carried out using the DAB (3,3’-diaminobenzidine) substrate (Vector Laboratories) for 10 min.

    Article Title: Disease-Associated Mutations of the STAT5B SH2 Domain Regulate Cytokine-Driven Enhancer Function and Mammary Development.
    Article Snippet: .. MACS2 [37] peak-finding algorithm was used to identify 1 3 Page 3 of 20 7 Journal of Mammary Gland Biology and Neoplasia (2025) 30:7 detected by overnight incubation with primary antibodies: STAT5A (1:200, Santa Cruz Biotechnology, sc-271542) and STAT5B (1:200, R&D Systems, AF1584) at room temperature. .. The slides were subsequently incubated with the appropriate secondary antibody (Goat anti-mouse or anti-rabbit IgG, Vector Laboratories, MP-7452 and MP-7451) for 1 h. Detection was carried out using the DAB (3,3’-diaminobenzidine) substrate (Vector Laboratories) for 10 min.

    Phospho-proteomics:

    Article Title: Capitalizing on paradoxical activation of the mitogen-activated protein kinase pathway for treatment of Imatinib-resistant mast cell leukemia.
    Article Snippet: DMSO was obtained from Carl Roth GmbH & Co. .. Pelleted cells were solubilized with 0.5% NP‐40% and 0.5% sodium deoxycholate in 4°C phosphorylation solubilization buffer.28 After normalizing for protein content, lysates were supplemented with Lämmli buffer, boiled for 5 min at 95°C and subjected to SDS‐PAGE and subsequent Western blot analysis as previously described.28 The following antibodies were used for detection of BRAF (F‐7, sc‐5284), CRAF (C‐12, sc‐133), KIT (M‐14, sc‐1494), STAT5a (A‐7, sc‐166479), PARP‐1 (H‐250, sc‐7150), GAPDH (6C5, sc‐32233) and were purchased from Santa Cruz, whereas antibodies used for detection of pKIT (Y719, #3391), ERK1/2 (L34F12, #4696), pERK1/2 (Thr202/ Tyr204, #4370), α‐pSTAT5 (Tyr694, #9351), α‐Caspase3 (#9662), cleaved Caspase3 (Asp175, #9664), α‐pMEK (Ser221, #2338) were purchased from Cell Signaling Technology. ..

    Western Blot:

    Article Title: Capitalizing on paradoxical activation of the mitogen-activated protein kinase pathway for treatment of Imatinib-resistant mast cell leukemia.
    Article Snippet: DMSO was obtained from Carl Roth GmbH & Co. .. Pelleted cells were solubilized with 0.5% NP‐40% and 0.5% sodium deoxycholate in 4°C phosphorylation solubilization buffer.28 After normalizing for protein content, lysates were supplemented with Lämmli buffer, boiled for 5 min at 95°C and subjected to SDS‐PAGE and subsequent Western blot analysis as previously described.28 The following antibodies were used for detection of BRAF (F‐7, sc‐5284), CRAF (C‐12, sc‐133), KIT (M‐14, sc‐1494), STAT5a (A‐7, sc‐166479), PARP‐1 (H‐250, sc‐7150), GAPDH (6C5, sc‐32233) and were purchased from Santa Cruz, whereas antibodies used for detection of pKIT (Y719, #3391), ERK1/2 (L34F12, #4696), pERK1/2 (Thr202/ Tyr204, #4370), α‐pSTAT5 (Tyr694, #9351), α‐Caspase3 (#9662), cleaved Caspase3 (Asp175, #9664), α‐pMEK (Ser221, #2338) were purchased from Cell Signaling Technology. ..



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