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mouse antihuman inhibin subunit antibody  (Bio-Rad)


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    Structured Review

    Bio-Rad mouse antihuman inhibin subunit antibody
    Fig. 2. <t>Inhibin</t> - and A-Subunit Products Secreted from CHO Cells Medium from inhibin-expressing CHO cells was TCA precipitated and examined <t>by</t> <t>immunoblot</t> analysis with the inhibin -subunit antibody (A) or the inhibin A-subunit antibody (B). C, Effect of tunicamycin on inhibin A secretion. CHO cells expressing inhibin A were incubated with vehicle (lanes 1 and 2) or 2.5 g/ml tunicamycin (lanes 3 and 4) and metabolically labeled. Medium was immunoprecipitated (IP) with anti--subunit (lanes 1 and 3) or anti-A-subunit antibody (lanes 2 and 4) and subjected to SDS-PAGE and autoradiography. *, Nonspecific nonglycosylated protein that immunoprecipitated only in tunicamycin-treated samples.
    Mouse Antihuman Inhibin Subunit Antibody, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 74 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse antihuman inhibin subunit antibody/product/Bio-Rad
    Average 93 stars, based on 74 article reviews
    mouse antihuman inhibin subunit antibody - by Bioz Stars, 2026-04
    93/100 stars

    Images

    1) Product Images from "N-linked oligosaccharides direct the differential assembly and secretion of inhibin alpha- and betaA-subunit dimers."

    Article Title: N-linked oligosaccharides direct the differential assembly and secretion of inhibin alpha- and betaA-subunit dimers.

    Journal: Molecular endocrinology (Baltimore, Md.)

    doi: 10.1210/me.2007-0050

    Fig. 2. Inhibin - and A-Subunit Products Secreted from CHO Cells Medium from inhibin-expressing CHO cells was TCA precipitated and examined by immunoblot analysis with the inhibin -subunit antibody (A) or the inhibin A-subunit antibody (B). C, Effect of tunicamycin on inhibin A secretion. CHO cells expressing inhibin A were incubated with vehicle (lanes 1 and 2) or 2.5 g/ml tunicamycin (lanes 3 and 4) and metabolically labeled. Medium was immunoprecipitated (IP) with anti--subunit (lanes 1 and 3) or anti-A-subunit antibody (lanes 2 and 4) and subjected to SDS-PAGE and autoradiography. *, Nonspecific nonglycosylated protein that immunoprecipitated only in tunicamycin-treated samples.
    Figure Legend Snippet: Fig. 2. Inhibin - and A-Subunit Products Secreted from CHO Cells Medium from inhibin-expressing CHO cells was TCA precipitated and examined by immunoblot analysis with the inhibin -subunit antibody (A) or the inhibin A-subunit antibody (B). C, Effect of tunicamycin on inhibin A secretion. CHO cells expressing inhibin A were incubated with vehicle (lanes 1 and 2) or 2.5 g/ml tunicamycin (lanes 3 and 4) and metabolically labeled. Medium was immunoprecipitated (IP) with anti--subunit (lanes 1 and 3) or anti-A-subunit antibody (lanes 2 and 4) and subjected to SDS-PAGE and autoradiography. *, Nonspecific nonglycosylated protein that immunoprecipitated only in tunicamycin-treated samples.

    Techniques Used: Expressing, Western Blot, Incubation, Metabolic Labelling, Labeling, Immunoprecipitation, SDS Page, Autoradiography



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    Fig. 2. <t>Inhibin</t> - and A-Subunit Products Secreted from CHO Cells Medium from inhibin-expressing CHO cells was TCA precipitated and examined <t>by</t> <t>immunoblot</t> analysis with the inhibin -subunit antibody (A) or the inhibin A-subunit antibody (B). C, Effect of tunicamycin on inhibin A secretion. CHO cells expressing inhibin A were incubated with vehicle (lanes 1 and 2) or 2.5 g/ml tunicamycin (lanes 3 and 4) and metabolically labeled. Medium was immunoprecipitated (IP) with anti--subunit (lanes 1 and 3) or anti-A-subunit antibody (lanes 2 and 4) and subjected to SDS-PAGE and autoradiography. *, Nonspecific nonglycosylated protein that immunoprecipitated only in tunicamycin-treated samples.
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    Image Search Results


    Fig. 2. Inhibin - and A-Subunit Products Secreted from CHO Cells Medium from inhibin-expressing CHO cells was TCA precipitated and examined by immunoblot analysis with the inhibin -subunit antibody (A) or the inhibin A-subunit antibody (B). C, Effect of tunicamycin on inhibin A secretion. CHO cells expressing inhibin A were incubated with vehicle (lanes 1 and 2) or 2.5 g/ml tunicamycin (lanes 3 and 4) and metabolically labeled. Medium was immunoprecipitated (IP) with anti--subunit (lanes 1 and 3) or anti-A-subunit antibody (lanes 2 and 4) and subjected to SDS-PAGE and autoradiography. *, Nonspecific nonglycosylated protein that immunoprecipitated only in tunicamycin-treated samples.

    Journal: Molecular endocrinology (Baltimore, Md.)

    Article Title: N-linked oligosaccharides direct the differential assembly and secretion of inhibin alpha- and betaA-subunit dimers.

    doi: 10.1210/me.2007-0050

    Figure Lengend Snippet: Fig. 2. Inhibin - and A-Subunit Products Secreted from CHO Cells Medium from inhibin-expressing CHO cells was TCA precipitated and examined by immunoblot analysis with the inhibin -subunit antibody (A) or the inhibin A-subunit antibody (B). C, Effect of tunicamycin on inhibin A secretion. CHO cells expressing inhibin A were incubated with vehicle (lanes 1 and 2) or 2.5 g/ml tunicamycin (lanes 3 and 4) and metabolically labeled. Medium was immunoprecipitated (IP) with anti--subunit (lanes 1 and 3) or anti-A-subunit antibody (lanes 2 and 4) and subjected to SDS-PAGE and autoradiography. *, Nonspecific nonglycosylated protein that immunoprecipitated only in tunicamycin-treated samples.

    Article Snippet: Immunoblot analysis was performed using the mouse antihuman inhibin -subunit antibody that recognizes amino acids 1–32 of the inhibin -subunit (Serotec, Raleigh, NC) or a polyclonal antibody specific for the inhibin A-subunit (provided by Dr. W. Vale, The Salk Institute, La Jolla, CA), followed by the appropriate secondary antibody conjugated to horseradish peroxidase (GE Healthcare, Little Chalfont, UK), and detected using ECL plus (GE Healthcare).

    Techniques: Expressing, Western Blot, Incubation, Metabolic Labelling, Labeling, Immunoprecipitation, SDS Page, Autoradiography