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Irs 2 antibody

Manufactured by Santa Cruz Biotechnology
Sourced in United States

The IRS-2 antibody is a research tool used to detect the insulin receptor substrate 2 (IRS-2) protein in various biological samples. IRS-2 is an important signaling molecule involved in insulin and growth factor receptor pathways. This antibody can be used to study the expression and distribution of IRS-2 in cells and tissues.

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2 protocols using irs 2 antibody

1

Signaling pathway analysis in cancer cells

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Growth media and supplements were purchased from Invitrogen (Grand Island, NY). IGF-I was purchased from GroPep (Adelaide, Australia). IGF-II was purchased from Gemini (Woodland, CA). Sulfasalazine (≥98%), L-Buthionine-sulfoximine (≥97%), N-Acetyl-L-cysteine, LY294002, U0126, and actin antibody were purchased from Sigma-Aldrich (St. Louis, MO). Humanized anti-IGF-IR monoclonal antibody huEM164 was generously provided by Immunogen Inc. (Norwood, MA). Antibodies for phosphorylated AKT serine 473, total and phospho-IGF-IR, total and phospho-phosphorylated p44/42 (MAPK), phospho-p38MAPK, and IRS-1 were purchased from Cell Signaling Technology (Beverly, MA). The IRS-2 antibody was purchased from Santa Cruz Biotechnology (Santa Cruz, CA). The xCT antibody for Western blot analysis was purchased from Novus Biologicals (Littleton, CO). Horseradish peroxidase-conjugated anti-phosphotyrosine (PY-20) was purchased from BD Biosciences (San Jose, CA). Anti-rabbit and anti-mouse horseradish peroxidase-conjugated secondary antibodies were purchased from Pierce (Rockford, IL). 5-(and-6)-carboxy-2′,7′-dichlorofluorescein diacetate was purchased from Invitrogen (Carlsbad, CA).
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2

Immunoprecipitation of IRS-2 in Granulosa Cells

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Control, and FSH-treated GCs were harvested in 20 mM Tris-HCl pH 7.5, 150 mM NaCl, 0.5% sodium deoxycholate, 1% Triton X-100, 2 mM EDTA and the extracts were prepared by homogenization. Equal amount of protein was taken for each sample and to the precleared supernatant, 10 l of IRS-2 antibody (Santa Cruz Biotechnology, USA) and protein-A agarose were added, and the mixture was kept for 15h at 4°C. Immune complexes were eluted from protein-A agarose and were subjected to Western blotting.
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