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rabbit polyclonal igf ii  (Santa Cruz Biotechnology)


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    Structured Review

    Santa Cruz Biotechnology rabbit polyclonal igf ii
    Rabbit Polyclonal Igf Ii, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 94/100, based on 363 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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    Average 94 stars, based on 363 article reviews
    rabbit polyclonal igf ii - by Bioz Stars, 2026-07
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    The microscopic findings [Hematoxylin and Eosin (H&E) staining and immunohistochemical staining of the resected tumor]. H&E staining (A) Low-power (×40) and (B) high-power (×400) views showed moderate stromal hypercellularity with mild nuclear atypia and mild pleomorphism of the spindle cells. Focal mildly atypical epithelial hyperplasia was also noted. Stromal overgrowth was absent. Immunohistochemical staining of (C) the phyllodes tumor and (D) normal breast tissue using rabbit <t>polyclonal</t> anti-insulin-like growth factor II <t>(IGF-II)</t> antibodies. The tumor cells, but not the normal breast tissue, were diffusely immunopositive for IGF-II.
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    A. and C. Relative mRNA expression <t>of</t> <t>IGF-II</t> in WT and HBx mouse livers (A) Mean ± SD ; * P< 0.05, ** P< 0.01, n =3, HepG2-Mock and HepG2-HBx cells (C) Mean + SD ; * P< 0.05, n =5-8. B. Immunohistochemistry images of 3-week-old WT and HBx-mouse livers stained with IGF-II. Original magnifications 40X. Data are representative of 3-5 mice per group. D. Secreted IGF-II protein levels from HepG2-Mock and HBx cells were measured. Mean ± SD ; * P< 0.05, n =6.
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    A. and C. Relative mRNA expression <t>of</t> <t>IGF-II</t> in WT and HBx mouse livers (A) Mean ± SD ; * P< 0.05, ** P< 0.01, n =3, HepG2-Mock and HepG2-HBx cells (C) Mean + SD ; * P< 0.05, n =5-8. B. Immunohistochemistry images of 3-week-old WT and HBx-mouse livers stained with IGF-II. Original magnifications 40X. Data are representative of 3-5 mice per group. D. Secreted IGF-II protein levels from HepG2-Mock and HBx cells were measured. Mean ± SD ; * P< 0.05, n =6.
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    Image Search Results


    The microscopic findings [Hematoxylin and Eosin (H&E) staining and immunohistochemical staining of the resected tumor]. H&E staining (A) Low-power (×40) and (B) high-power (×400) views showed moderate stromal hypercellularity with mild nuclear atypia and mild pleomorphism of the spindle cells. Focal mildly atypical epithelial hyperplasia was also noted. Stromal overgrowth was absent. Immunohistochemical staining of (C) the phyllodes tumor and (D) normal breast tissue using rabbit polyclonal anti-insulin-like growth factor II (IGF-II) antibodies. The tumor cells, but not the normal breast tissue, were diffusely immunopositive for IGF-II.

    Journal: Internal Medicine

    Article Title: A Hypoglycemia-inducing Giant Borderline Phyllodes Tumor Secreting High-molecular-weight Insulin-Like Growth Factor II: Immunohistochemistry and a Western Blot Analysis

    doi: 10.2169/internalmedicine.9287-17

    Figure Lengend Snippet: The microscopic findings [Hematoxylin and Eosin (H&E) staining and immunohistochemical staining of the resected tumor]. H&E staining (A) Low-power (×40) and (B) high-power (×400) views showed moderate stromal hypercellularity with mild nuclear atypia and mild pleomorphism of the spindle cells. Focal mildly atypical epithelial hyperplasia was also noted. Stromal overgrowth was absent. Immunohistochemical staining of (C) the phyllodes tumor and (D) normal breast tissue using rabbit polyclonal anti-insulin-like growth factor II (IGF-II) antibodies. The tumor cells, but not the normal breast tissue, were diffusely immunopositive for IGF-II.

    Article Snippet: They were probed with rabbit polyclonal anti-IGF-II antibody (Atlas Antibodies, Bromma, Sweden).

    Techniques: Staining, Immunohistochemical staining

    Western blotting of high-molecular-weight IGF-II. Lane 1, serum from a healthy control; lane 2, serum from the patient collected preoperatively; lane 3, serum obtained 3 days after the resection of the tumor; lane 4, phyllodes tumor tissue. Large amounts of high-molecular-weight IGF-II were detected in the serum collected preoperatively (lane 2) and in the tumor tissue (lane 4) but not in serum collected postoperatively (lane 3) or a serum sample from a healthy control (lane 1).

    Journal: Internal Medicine

    Article Title: A Hypoglycemia-inducing Giant Borderline Phyllodes Tumor Secreting High-molecular-weight Insulin-Like Growth Factor II: Immunohistochemistry and a Western Blot Analysis

    doi: 10.2169/internalmedicine.9287-17

    Figure Lengend Snippet: Western blotting of high-molecular-weight IGF-II. Lane 1, serum from a healthy control; lane 2, serum from the patient collected preoperatively; lane 3, serum obtained 3 days after the resection of the tumor; lane 4, phyllodes tumor tissue. Large amounts of high-molecular-weight IGF-II were detected in the serum collected preoperatively (lane 2) and in the tumor tissue (lane 4) but not in serum collected postoperatively (lane 3) or a serum sample from a healthy control (lane 1).

    Article Snippet: They were probed with rabbit polyclonal anti-IGF-II antibody (Atlas Antibodies, Bromma, Sweden).

    Techniques: Western Blot, High Molecular Weight, Control

    A. and C. Relative mRNA expression of IGF-II in WT and HBx mouse livers (A) Mean ± SD ; * P< 0.05, ** P< 0.01, n =3, HepG2-Mock and HepG2-HBx cells (C) Mean + SD ; * P< 0.05, n =5-8. B. Immunohistochemistry images of 3-week-old WT and HBx-mouse livers stained with IGF-II. Original magnifications 40X. Data are representative of 3-5 mice per group. D. Secreted IGF-II protein levels from HepG2-Mock and HBx cells were measured. Mean ± SD ; * P< 0.05, n =6.

    Journal: Oncotarget

    Article Title: IGF-II induced by hepatitis B virus X protein regulates EMT via SUMO mediated loss of E-cadherin in mice

    doi: 10.18632/oncotarget.10922

    Figure Lengend Snippet: A. and C. Relative mRNA expression of IGF-II in WT and HBx mouse livers (A) Mean ± SD ; * P< 0.05, ** P< 0.01, n =3, HepG2-Mock and HepG2-HBx cells (C) Mean + SD ; * P< 0.05, n =5-8. B. Immunohistochemistry images of 3-week-old WT and HBx-mouse livers stained with IGF-II. Original magnifications 40X. Data are representative of 3-5 mice per group. D. Secreted IGF-II protein levels from HepG2-Mock and HBx cells were measured. Mean ± SD ; * P< 0.05, n =6.

    Article Snippet: Samples were incubated overnight at 4 °C with anti-IGF-II rabbit polyclonal antibody (1:200; Santa Cruz Biotechnology, CA, USA).

    Techniques: Expressing, Immunohistochemistry, Staining

    Mean ± SD ; * P< 0.05, n =6. B. Cell growth was measured in HepG2-Mock cells treated with conditioned medium from HepG2-Mock (CM-Mock), and HBx (CM-HBx). Mean ± SD ; * P < 0.05, n=6. C. Cell numbers were quantified in HepG2-Mock and HBx cells with or without anti-IGF-II. Mean ± SD ; ** P< 0.01, n =4. D. Multilayer growth of HepG2-HBx cells were reversed to monolayer growth with anti-IGF-II.

    Journal: Oncotarget

    Article Title: IGF-II induced by hepatitis B virus X protein regulates EMT via SUMO mediated loss of E-cadherin in mice

    doi: 10.18632/oncotarget.10922

    Figure Lengend Snippet: Mean ± SD ; * P< 0.05, n =6. B. Cell growth was measured in HepG2-Mock cells treated with conditioned medium from HepG2-Mock (CM-Mock), and HBx (CM-HBx). Mean ± SD ; * P < 0.05, n=6. C. Cell numbers were quantified in HepG2-Mock and HBx cells with or without anti-IGF-II. Mean ± SD ; ** P< 0.01, n =4. D. Multilayer growth of HepG2-HBx cells were reversed to monolayer growth with anti-IGF-II.

    Article Snippet: Samples were incubated overnight at 4 °C with anti-IGF-II rabbit polyclonal antibody (1:200; Santa Cruz Biotechnology, CA, USA).

    Techniques: