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rabbit polyclonal anti igf ii antibody  (Atlas Antibodies)


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    Atlas Antibodies rabbit polyclonal anti igf ii antibody
    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.
    Rabbit Polyclonal Anti Igf Ii Antibody, supplied by Atlas Antibodies, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+polyclonal+anti+igf+ii+antibody/pmc05820043-57-4-8?v=Atlas+Antibodies
    Average 86 stars, based on 1 article reviews
    rabbit polyclonal anti igf ii antibody - by Bioz Stars, 2026-08
    86/100 stars

    Images

    1) Product Images from "A Hypoglycemia-inducing Giant Borderline Phyllodes Tumor Secreting High-molecular-weight Insulin-Like Growth Factor II: Immunohistochemistry and a Western Blot Analysis"

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

    Journal: Internal Medicine

    doi: 10.2169/internalmedicine.9287-17

    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.
    Figure Legend 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.

    Techniques Used: 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).
    Figure Legend 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).

    Techniques Used: Western Blot, High Molecular Weight, Control



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    Fig. <t>1.</t> <t>IGF-2</t> morpholinos efficiently and specifically knockdown IGF-2 in vivo. (A) Phenotype of (a) control injected and (b) IGF-2(a+b) morphant embryo at 24 hpf. IGF-2(a+b) morphant embryos are ventralised with a shorter body, disrupted brain structures (double arrows), reduced eyes, disrupted somites and an expanded intermediate cell mass (arrow). (B) Western blot showing IGF-2 and alpha-tubulin at 24 hpf in (1) uninjected control embryos, (2) embryos injected with control morpholinos or (3) embryos injected with IGF-2(a+b) morpholinos. (C) Igf-2a and igf-2b mediate their effects on development in a synergistic fashion. (D) Co-injection of igf-2a or igf-2b RNA with the corresponding morpholino rescues the IGF-2 morphant phenotype. Rescued embryos display normal body size, eyes and brain structures at 24 hpf. Results shown are a summary of three independent experiments (n ≥ 80). Error bars indicate the standard deviation of the mean.
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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:

    Fig. 1. IGF-2 morpholinos efficiently and specifically knockdown IGF-2 in vivo. (A) Phenotype of (a) control injected and (b) IGF-2(a+b) morphant embryo at 24 hpf. IGF-2(a+b) morphant embryos are ventralised with a shorter body, disrupted brain structures (double arrows), reduced eyes, disrupted somites and an expanded intermediate cell mass (arrow). (B) Western blot showing IGF-2 and alpha-tubulin at 24 hpf in (1) uninjected control embryos, (2) embryos injected with control morpholinos or (3) embryos injected with IGF-2(a+b) morpholinos. (C) Igf-2a and igf-2b mediate their effects on development in a synergistic fashion. (D) Co-injection of igf-2a or igf-2b RNA with the corresponding morpholino rescues the IGF-2 morphant phenotype. Rescued embryos display normal body size, eyes and brain structures at 24 hpf. Results shown are a summary of three independent experiments (n ≥ 80). Error bars indicate the standard deviation of the mean.

    Journal: The International journal of developmental biology

    Article Title: Insulin-like growth factor-2 regulates early neural and cardiovascular system development in zebrafish embryos.

    doi: 10.1387/ijdb.092922lh

    Figure Lengend Snippet: Fig. 1. IGF-2 morpholinos efficiently and specifically knockdown IGF-2 in vivo. (A) Phenotype of (a) control injected and (b) IGF-2(a+b) morphant embryo at 24 hpf. IGF-2(a+b) morphant embryos are ventralised with a shorter body, disrupted brain structures (double arrows), reduced eyes, disrupted somites and an expanded intermediate cell mass (arrow). (B) Western blot showing IGF-2 and alpha-tubulin at 24 hpf in (1) uninjected control embryos, (2) embryos injected with control morpholinos or (3) embryos injected with IGF-2(a+b) morpholinos. (C) Igf-2a and igf-2b mediate their effects on development in a synergistic fashion. (D) Co-injection of igf-2a or igf-2b RNA with the corresponding morpholino rescues the IGF-2 morphant phenotype. Rescued embryos display normal body size, eyes and brain structures at 24 hpf. Results shown are a summary of three independent experiments (n ≥ 80). Error bars indicate the standard deviation of the mean.

    Article Snippet: The membrane was incubated with primary antibodies rabbit anti-IGF-2 (1:1000, Gropep PAAA1) or mouse anti-α-tubulin (1:2000, Sigma) and then with the secondary antibodies rabbit peroxidase-conjugated (1:140,000, Sigma) or mouse peroxidase-conjugated (1:8000, Sigma).

    Techniques: Knockdown, In Vivo, Control, Injection, Western Blot, Standard Deviation

    Fig. 3. IGF-2 regulates the expression of genes involved in dorsal-ventral patterning. (A,C) Embryos injected with control morpholinos show normal chordin and goosecoid expression. (B,D) Expression of chordin and goosecoid is reduced in IGF-2(a+b) morphant embryos (arrows). (E,G,I) Embryos injected with control morpholinos show normal bmp2b, bmp4 and gata2 expression. (F,H,J) Expression of bmp2b, bmp4 and gata2 is expanded towards the dorsal side in IGF-2(a+b) morphant embryos (asterisks). Frequency of embryos displaying this staining pattern; B, 13/26; D, 17/31; F, 16/25; H, 18/32; J, 26/34. All embryos are shown in a lateral view.

    Journal: The International journal of developmental biology

    Article Title: Insulin-like growth factor-2 regulates early neural and cardiovascular system development in zebrafish embryos.

    doi: 10.1387/ijdb.092922lh

    Figure Lengend Snippet: Fig. 3. IGF-2 regulates the expression of genes involved in dorsal-ventral patterning. (A,C) Embryos injected with control morpholinos show normal chordin and goosecoid expression. (B,D) Expression of chordin and goosecoid is reduced in IGF-2(a+b) morphant embryos (arrows). (E,G,I) Embryos injected with control morpholinos show normal bmp2b, bmp4 and gata2 expression. (F,H,J) Expression of bmp2b, bmp4 and gata2 is expanded towards the dorsal side in IGF-2(a+b) morphant embryos (asterisks). Frequency of embryos displaying this staining pattern; B, 13/26; D, 17/31; F, 16/25; H, 18/32; J, 26/34. All embryos are shown in a lateral view.

    Article Snippet: The membrane was incubated with primary antibodies rabbit anti-IGF-2 (1:1000, Gropep PAAA1) or mouse anti-α-tubulin (1:2000, Sigma) and then with the secondary antibodies rabbit peroxidase-conjugated (1:140,000, Sigma) or mouse peroxidase-conjugated (1:8000, Sigma).

    Techniques: Expressing, Injection, Control, Staining

    Fig. 2. IGF-2 is required for the development of anterior neural structures during gastrulation and plays an anti-apoptotic role during segmentation. (A,C) Control morpholino injected embryos show normal pax6.2 and rx3 expression. (B,D) IGF-2(a+b) morphant embryos show reductions in pax6.2 and rx3 expression. (E) Embryos injected with control morpholinos show low levels of apoptosis during zebrafish segmentation. (F) Knockdown of igf-2a and igf-2b results in an increase in apoptosis in the anterior region of the embryo and in the developing spinal cord. Frequency of embryos displaying this staining pattern; B, 14/ 32; D, 22/40; F, 17/28. (A-D) are views of the future anterior region; (E,F) are lateral views.

    Journal: The International journal of developmental biology

    Article Title: Insulin-like growth factor-2 regulates early neural and cardiovascular system development in zebrafish embryos.

    doi: 10.1387/ijdb.092922lh

    Figure Lengend Snippet: Fig. 2. IGF-2 is required for the development of anterior neural structures during gastrulation and plays an anti-apoptotic role during segmentation. (A,C) Control morpholino injected embryos show normal pax6.2 and rx3 expression. (B,D) IGF-2(a+b) morphant embryos show reductions in pax6.2 and rx3 expression. (E) Embryos injected with control morpholinos show low levels of apoptosis during zebrafish segmentation. (F) Knockdown of igf-2a and igf-2b results in an increase in apoptosis in the anterior region of the embryo and in the developing spinal cord. Frequency of embryos displaying this staining pattern; B, 14/ 32; D, 22/40; F, 17/28. (A-D) are views of the future anterior region; (E,F) are lateral views.

    Article Snippet: The membrane was incubated with primary antibodies rabbit anti-IGF-2 (1:1000, Gropep PAAA1) or mouse anti-α-tubulin (1:2000, Sigma) and then with the secondary antibodies rabbit peroxidase-conjugated (1:140,000, Sigma) or mouse peroxidase-conjugated (1:8000, Sigma).

    Techniques: Control, Injection, Expressing, Knockdown, Staining

    Fig. 4. Blood circulation is disrupted when IGF signalling is reduced. (A) Control morpholino injected embryos stained with O-dianisidine at 72 hpf show normal blood circulation. (B) IGF-2(a+b) morphant embryo with reduced circulating blood. Grey arrows indicate blood in the heart region, red arrows blood circulation in the intersomitic vesicles and grey arrowheads the intermediate cell mass. (C,F) Embryos injected with control morpholinos showing normal scl and gata1 expression at 26 hpf. (D,G) Knockdown of igf-2a and igf-2b results in an increase in scl and gata1 expression and an expansion of expression outside the intermediate cell mass. (E,H) DN-IGF-1R injected embryos show an increase in scl and gata1 expression. Arrowhead indicates position of intermediate cell mass and arrows indicate extent of expression along the embryo. Frequency of embryos displaying this staining pattern; B, 73/86; D, 37/48; E, 30/30; G, 48/58; H, 26/29. All embryos are shown in lateral view.

    Journal: The International journal of developmental biology

    Article Title: Insulin-like growth factor-2 regulates early neural and cardiovascular system development in zebrafish embryos.

    doi: 10.1387/ijdb.092922lh

    Figure Lengend Snippet: Fig. 4. Blood circulation is disrupted when IGF signalling is reduced. (A) Control morpholino injected embryos stained with O-dianisidine at 72 hpf show normal blood circulation. (B) IGF-2(a+b) morphant embryo with reduced circulating blood. Grey arrows indicate blood in the heart region, red arrows blood circulation in the intersomitic vesicles and grey arrowheads the intermediate cell mass. (C,F) Embryos injected with control morpholinos showing normal scl and gata1 expression at 26 hpf. (D,G) Knockdown of igf-2a and igf-2b results in an increase in scl and gata1 expression and an expansion of expression outside the intermediate cell mass. (E,H) DN-IGF-1R injected embryos show an increase in scl and gata1 expression. Arrowhead indicates position of intermediate cell mass and arrows indicate extent of expression along the embryo. Frequency of embryos displaying this staining pattern; B, 73/86; D, 37/48; E, 30/30; G, 48/58; H, 26/29. All embryos are shown in lateral view.

    Article Snippet: The membrane was incubated with primary antibodies rabbit anti-IGF-2 (1:1000, Gropep PAAA1) or mouse anti-α-tubulin (1:2000, Sigma) and then with the secondary antibodies rabbit peroxidase-conjugated (1:140,000, Sigma) or mouse peroxidase-conjugated (1:8000, Sigma).

    Techniques: Control, Injection, Staining, Expressing, Knockdown

    Fig. 5. Angiogenesis is compromised when IGF signalling is reduced. (A- D) fli1:EGFP transgenic em- bryos injected with control morpholinos showing normal vascular development. (E-H) Class I IGF-2 morphant em- bryo. The intensity of GFP expressing cells in the head and eyes is reduced while the basic pattern of vasculature remains intact. The intermediate cell mass is mildly expanded and the intersomitic vessels are reduced. By 72 hpf, the parachordal vessel is incompletely formed. (I-L) Class II IGF-2 morphant embryo. The sprouting of vessels in the head and eyes are reduced. Intersomitic vessel sprouting is irregular and reduced, the intermediate cell mass is expanded and the parachordal vessel is disrupted. (M,N) Control embryo at 26 hpf showing normal expression of flk1 in the vasculature. (O,P) Angiogenesis is disrupted in DN-IGF-1R injected embryos as shown by flk1 expression (n=14/29). White arrows indicate the vasculature in the head and eyes. White arrowheads point to the intersomitic vessels, red arrow points to the intermediate cell mass and the grey arrow indicates the parachordal vessel. All embryos are shown in a lateral view.

    Journal: The International journal of developmental biology

    Article Title: Insulin-like growth factor-2 regulates early neural and cardiovascular system development in zebrafish embryos.

    doi: 10.1387/ijdb.092922lh

    Figure Lengend Snippet: Fig. 5. Angiogenesis is compromised when IGF signalling is reduced. (A- D) fli1:EGFP transgenic em- bryos injected with control morpholinos showing normal vascular development. (E-H) Class I IGF-2 morphant em- bryo. The intensity of GFP expressing cells in the head and eyes is reduced while the basic pattern of vasculature remains intact. The intermediate cell mass is mildly expanded and the intersomitic vessels are reduced. By 72 hpf, the parachordal vessel is incompletely formed. (I-L) Class II IGF-2 morphant embryo. The sprouting of vessels in the head and eyes are reduced. Intersomitic vessel sprouting is irregular and reduced, the intermediate cell mass is expanded and the parachordal vessel is disrupted. (M,N) Control embryo at 26 hpf showing normal expression of flk1 in the vasculature. (O,P) Angiogenesis is disrupted in DN-IGF-1R injected embryos as shown by flk1 expression (n=14/29). White arrows indicate the vasculature in the head and eyes. White arrowheads point to the intersomitic vessels, red arrow points to the intermediate cell mass and the grey arrow indicates the parachordal vessel. All embryos are shown in a lateral view.

    Article Snippet: The membrane was incubated with primary antibodies rabbit anti-IGF-2 (1:1000, Gropep PAAA1) or mouse anti-α-tubulin (1:2000, Sigma) and then with the secondary antibodies rabbit peroxidase-conjugated (1:140,000, Sigma) or mouse peroxidase-conjugated (1:8000, Sigma).

    Techniques: Transgenic Assay, Injection, Control, Expressing