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polyclonal anti insulin receptor beta subunit  (Santa Cruz Biotechnology)


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    Santa Cruz Biotechnology polyclonal anti insulin receptor beta subunit
    IR and IGF-1R content and phosphorylation in placental tissues. Insulin receptor protein content was detected by immunoblotting with a <t>polyclonal</t> anti-insulin receptor β-subunit. (A) The protein content of IGF-1R in placenta samples was detected by immunoblotting using a polyclonal anti-IGF-1R β-subunit. (B) Solubilized placental tissues were subjected to immunoprecipitation with an anti-IR or anti IGF-1R. The resulting immune complexes were resolved by SDS-PAGE and immunoblotting with an anti-PY antibody to detect receptor phosphorylation (A, B) . Protein content was normalized against β-actin, whereas phosphorylated proteins were normalized against their total amount. Each bar represents mean ± SE of all placental samples (n=40 for NGT, n=20 for GDM and n=20 for T1D). A representative Western-blot is included in the bottom (five different patients for each group). IR-A mRNA expression in placental tissue measured by RT-PCR. The bar graphs show the quantitation of IR-A mRNA (mean ± SE) in all samples for each group (C) . *p < 0.05; **p < 0.001, after adjusting, in multivariate logistic regression models, for age, pre-pregnancy BMI, gestational age at delivery and type of delivery.
    Polyclonal Anti Insulin Receptor Beta Subunit, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1851 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/insulin+receptor+subunit+polyclonal/pmc07988311-83-0-7?v=Santa+Cruz+Biotechnology
    Average 96 stars, based on 1851 article reviews
    polyclonal anti insulin receptor beta subunit - by Bioz Stars, 2026-07
    96/100 stars

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    1) Product Images from "Maternal Diabetes Impairs Insulin and IGF-1 Receptor Expression and Signaling in Human Placenta"

    Article Title: Maternal Diabetes Impairs Insulin and IGF-1 Receptor Expression and Signaling in Human Placenta

    Journal: Frontiers in Endocrinology

    doi: 10.3389/fendo.2021.621680

    IR and IGF-1R content and phosphorylation in placental tissues. Insulin receptor protein content was detected by immunoblotting with a polyclonal anti-insulin receptor β-subunit. (A) The protein content of IGF-1R in placenta samples was detected by immunoblotting using a polyclonal anti-IGF-1R β-subunit. (B) Solubilized placental tissues were subjected to immunoprecipitation with an anti-IR or anti IGF-1R. The resulting immune complexes were resolved by SDS-PAGE and immunoblotting with an anti-PY antibody to detect receptor phosphorylation (A, B) . Protein content was normalized against β-actin, whereas phosphorylated proteins were normalized against their total amount. Each bar represents mean ± SE of all placental samples (n=40 for NGT, n=20 for GDM and n=20 for T1D). A representative Western-blot is included in the bottom (five different patients for each group). IR-A mRNA expression in placental tissue measured by RT-PCR. The bar graphs show the quantitation of IR-A mRNA (mean ± SE) in all samples for each group (C) . *p < 0.05; **p < 0.001, after adjusting, in multivariate logistic regression models, for age, pre-pregnancy BMI, gestational age at delivery and type of delivery.
    Figure Legend Snippet: IR and IGF-1R content and phosphorylation in placental tissues. Insulin receptor protein content was detected by immunoblotting with a polyclonal anti-insulin receptor β-subunit. (A) The protein content of IGF-1R in placenta samples was detected by immunoblotting using a polyclonal anti-IGF-1R β-subunit. (B) Solubilized placental tissues were subjected to immunoprecipitation with an anti-IR or anti IGF-1R. The resulting immune complexes were resolved by SDS-PAGE and immunoblotting with an anti-PY antibody to detect receptor phosphorylation (A, B) . Protein content was normalized against β-actin, whereas phosphorylated proteins were normalized against their total amount. Each bar represents mean ± SE of all placental samples (n=40 for NGT, n=20 for GDM and n=20 for T1D). A representative Western-blot is included in the bottom (five different patients for each group). IR-A mRNA expression in placental tissue measured by RT-PCR. The bar graphs show the quantitation of IR-A mRNA (mean ± SE) in all samples for each group (C) . *p < 0.05; **p < 0.001, after adjusting, in multivariate logistic regression models, for age, pre-pregnancy BMI, gestational age at delivery and type of delivery.

    Techniques Used: Phospho-proteomics, Western Blot, Immunoprecipitation, SDS Page, Expressing, Reverse Transcription Polymerase Chain Reaction, Quantitation Assay



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    Image Search Results


    IR and IGF-1R content and phosphorylation in placental tissues. Insulin receptor protein content was detected by immunoblotting with a polyclonal anti-insulin receptor β-subunit. (A) The protein content of IGF-1R in placenta samples was detected by immunoblotting using a polyclonal anti-IGF-1R β-subunit. (B) Solubilized placental tissues were subjected to immunoprecipitation with an anti-IR or anti IGF-1R. The resulting immune complexes were resolved by SDS-PAGE and immunoblotting with an anti-PY antibody to detect receptor phosphorylation (A, B) . Protein content was normalized against β-actin, whereas phosphorylated proteins were normalized against their total amount. Each bar represents mean ± SE of all placental samples (n=40 for NGT, n=20 for GDM and n=20 for T1D). A representative Western-blot is included in the bottom (five different patients for each group). IR-A mRNA expression in placental tissue measured by RT-PCR. The bar graphs show the quantitation of IR-A mRNA (mean ± SE) in all samples for each group (C) . *p < 0.05; **p < 0.001, after adjusting, in multivariate logistic regression models, for age, pre-pregnancy BMI, gestational age at delivery and type of delivery.

    Journal: Frontiers in Endocrinology

    Article Title: Maternal Diabetes Impairs Insulin and IGF-1 Receptor Expression and Signaling in Human Placenta

    doi: 10.3389/fendo.2021.621680

    Figure Lengend Snippet: IR and IGF-1R content and phosphorylation in placental tissues. Insulin receptor protein content was detected by immunoblotting with a polyclonal anti-insulin receptor β-subunit. (A) The protein content of IGF-1R in placenta samples was detected by immunoblotting using a polyclonal anti-IGF-1R β-subunit. (B) Solubilized placental tissues were subjected to immunoprecipitation with an anti-IR or anti IGF-1R. The resulting immune complexes were resolved by SDS-PAGE and immunoblotting with an anti-PY antibody to detect receptor phosphorylation (A, B) . Protein content was normalized against β-actin, whereas phosphorylated proteins were normalized against their total amount. Each bar represents mean ± SE of all placental samples (n=40 for NGT, n=20 for GDM and n=20 for T1D). A representative Western-blot is included in the bottom (five different patients for each group). IR-A mRNA expression in placental tissue measured by RT-PCR. The bar graphs show the quantitation of IR-A mRNA (mean ± SE) in all samples for each group (C) . *p < 0.05; **p < 0.001, after adjusting, in multivariate logistic regression models, for age, pre-pregnancy BMI, gestational age at delivery and type of delivery.

    Article Snippet: Polyclonal anti-insulin receptor beta-subunit was purchased from Santa Cruz Biotechnology, Inc. (Santa Cruz, CA).

    Techniques: Phospho-proteomics, Western Blot, Immunoprecipitation, SDS Page, Expressing, Reverse Transcription Polymerase Chain Reaction, Quantitation Assay