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GAP1-InsP4 BP Antibody (E-7): sc-398127

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Datasheets
  • GAP1-InsP4 BP Antibody (E-7) is a mouse monoclonal IgG1 κ provided at 200 µg/ml
  • specific for an epitope mapping between amino acids 104-129 near the N-terminus of GAP1-InsP4 BP of human origin
  • recommended for detection of GAP1-InsP4 BP of mouse, rat, human and avian origin by WB, IP, IF and ELISA; also reactive with additional species, including and equine, canine, bovine, porcine and avian
  • m-IgG Fc BP-HRP, m-IgG1 BP-HRP and m-IgGκ BP-HRP are the preferred secondary detection reagents for GAP1-InsP4 BP Antibody (E-7) for WB applications. These reagents are now offered in bundles with GAP1-InsP4 BP Antibody (E-7) (see ordering information below).

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    GAP1-InsP4 BP Antibody (E-7) is a mouse monoclonal IgG1 antibody that detects GAP1-InsP4 BP in mouse, rat, and human samples through applications such as western blotting (WB), immunoprecipitation (IP), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA). GAP1-InsP4 BP, also known as Ras p21 protein activator (GTPase-activating protein) 3, is a crucial 829-amino acid protein that plays a significant role in cellular signaling by binding phospholipids in both calcium-dependent and -independent manners. GAP1-InsP4 BP is part of the Ras GTPase-activating protein family, which includes four distinct genes, and features an N-terminal tandem C2 domain, a GAP-related domain, and a C-terminal pleckstrin homology (PH) domain. The structure of GAP1-InsP4 BP is particularly important as PH domains are essential for membrane targeting, allowing GAP1-InsP4 BP to bind specific phospholipids. Upon stimulation by agonists that promote the production of phosphatidylinositol 3,4,5-trisphosphate, GAP1-InsP4 BP selectively interacts with inositol phosphates, facilitating localization to the plasma membrane. This interaction is vital for the regulation of various signaling pathways, underscoring GAP1-InsP4 BP′s importance in cellular function and communication.

    For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.

    Alexa Fluor® is a trademark of Molecular Probes Inc., OR., USA

    LI-COR® and Odyssey® are registered trademarks of LI-COR Biosciences

    GAP1-InsP4 BP Antibody (E-7) References:

    1. Twenty bone-mineral-density loci identified by large-scale meta-analysis of genome-wide association studies.  |  Rivadeneira, F., et al. 2009. Nat Genet. 41: 1199-206. PMID: 19801982
    2. Staphylococcus aureus recruits Cdc42GAP through recycling endosomes and the exocyst to invade human endothelial cells.  |  Rauch, L., et al. 2016. J Cell Sci. 129: 2937-49. PMID: 27311480
    3. Targeted sequencing of genome wide significant loci associated with bone mineral density (BMD) reveals significant novel and rare variants: the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) targeted sequencing study.  |  Hsu, YH., et al. 2016. Hum Mol Genet. 25: 5234-5243. PMID: 27616567
    4. SLIT2/ROBO2 signaling pathway inhibits nonmuscle myosin IIA activity and destabilizes kidney podocyte adhesion.  |  Fan, X., et al. 2016. JCI Insight. 1: e86934. PMID: 27882344
    5. Comparison of Peptide- and Lipid-Based Delivery of miR-34a-5p Mimic into PPC-1 Cells.  |  Urgard, E., et al. 2017. Nucleic Acid Ther. 27: 295-302. PMID: 28657476
    6. miR-130b directly targets ARHGAP1 to drive activation of a metastatic CDC42-PAK1-AP1 positive feedback loop in Ewing sarcoma.  |  Satterfield, L., et al. 2017. Int J Cancer. 141: 2062-2075. PMID: 28748534
    7. Cancer-secreted hsa-miR-940 induces an osteoblastic phenotype in the bone metastatic microenvironment via targeting ARHGAP1 and FAM134A.  |  Hashimoto, K., et al. 2018. Proc Natl Acad Sci U S A. 115: 2204-2209. PMID: 29440427
    8. MicroRNA-509-3p inhibits cellular migration, invasion, and proliferation, and sensitizes osteosarcoma to cisplatin.  |  Patil, SL., et al. 2019. Sci Rep. 9: 19089. PMID: 31836741
    9. Whole-genome sequencing unravels novel genetic determinants and regulatory pathways associated with triamcinolone acetonide-induced ocular hypertension.  |  Badrinarayanan, L., et al. 2023. Mol Genet Genomics. 298: 13-26. PMID: 36222912
    10. Purification of time-resolved insulin granules reveals proteomic and lipidomic changes during granule aging.  |  Neukam, M., et al. 2024. Cell Rep. 43: 113836. PMID: 38421874

    Ordering Information

    Product NameCatalog #UNITPriceQtyFAVORITES

    GAP1-InsP4 BP Antibody (E-7)

    sc-398127
    200 µg/ml
    $322.00

    GAP1-InsP4 BP Antibody (E-7): m-IgG Fc BP-HRP Bundle

    sc-538374
    200 µg Ab; 10 µg BP
    $361.00

    GAP1-InsP4 BP Antibody (E-7): m-IgGκ BP-HRP Bundle

    sc-535977
    200 µg Ab; 40 µg BP
    $361.00

    GAP1-InsP4 BP Antibody (E-7): m-IgG1 BP-HRP Bundle

    sc-545668
    200 µg Ab; 20 µg BP
    $361.00

    GAP1-InsP4 BP (E-7) Neutralizing Peptide

    sc-398127 P
    100 µg/0.5 ml
    $69.00

    What application is the blocking peptide sc-398127 P appropriate for?

    Asked by: Cweed
    Thank you for your question. The blocking peptide is intended for use as a negative control, by pre-adsorbing the mouse monoclonal antibody against the antigen. For full protocol details, please contact our Technical Services Department or view our online protocol here: https://www.scbt.com/scbt/resources/protocols/peptide-neutralization
    Answered by: Technical Support
    Date published: 2017-02-27
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    Rated 5 out of 5 by from Produced positive Western blot data of GAP1Produced positive Western blot data of GAP1-InsP4 BP expression in non-transfected 293T, human GAP1-InsP4 BP transfected 293T whole cell lysates, human platelet extract, HeLa and IMR-32 whole cell lysates. -SCBT QC
    Date published: 2013-08-06
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    GAP1-InsP 4 BP Antibody (E-7) is rated 5.0 out of 5 by 1.
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