Merck Millipore代理MAB2630 Anti-KRIT-1 Antibody, clone 15;store at +2℃ to +8℃

2025-06-29

货号:MAB2630

品牌:Merck Millipore

规格:100Ug

目录价:¥5666.00

市场价格:¥4816.10

会员价格:¥4532.80

金山科研平台,产品价格货期咨询微信:jinshanbio Description: Anti-KRIT-1 Antibody, clone 15 | MAB2630 View All» Promotional Text: Special Shipping Offer on Antibodies100% Performance Guaranteed View All» Specificity: The antibody recognizes KRIT-1. View All» Molecular Weight: ~ 84 kDa View All» Epitope: FERM domain View All» Immunogen: GST-tagged recombinant protein corresponding to human KRIT-1 at and around the FERM domain. View All» Clone: 15B2 View All» Isotype: IgG2bκ View All» Background Information: Cerebral cavernous malformation (CCM), a disease associated with defective endothelial junctions, results from autosomal dominant CCM1 mutations that cause a loss of KRIT-1 protein function. CCM1 has been identified as the KRIT-1 gene. The protein product, KRIT-1, also known as Krev interaction trapped protein 1, is a microtubule-associated protein involved in endothelial cell-cell and cell-extracellular matrix interactions. KRIT-1 binds to Rap1 that maintains the integrity of endothelial junctions. It is reported that KRIT-1 colocalizes and is physically associated with junctional proteins via its band 4.1/ezrin/radixin/moesin (FERM) domain, (Glading, 2007). View All» Species Reactivity: Human View All» Species Reactivity Note: Demonstrated to react in human. View All» Control: HeLa, A431, and HUVECs. View All» Quality Assurance: Immunocytochemistry Analysis: 1:500 dilution of this antibody detected KRIT-1 in HeLa, A431, and HUVECs. View All» Purification Method: Protein G purfied View All» Presentation: Purified mouse monoclonal IgG2bκ in buffer containing 0.1 M Tris-Glycine (pH 7.4, 150 mM NaCl) with 0.05% sodium azide. View All» Storage Conditions: Stable for 1 year at 2-8°C from date of receipt. View All» UniProt Number: O00522 View All» Entrez Gene Number: NP_919436.1 View All» Gene Symbol:

  • KRIT1

  • CAM

  • CCM1

    View All» Alternate Names:
    • Cerebral cavernous malformations 1 protein

    • Krev interaction trapped 1

      View All» Usage Statement: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. View All» Key Applications:
      • Immunocytochemistry

      • Immunoprecipitation

        View All» Entrez Gene Summary: This gene encodes a protein containing four ankyrin repeats, a band 4.1/ezrin/radixin/moesin (FERM) domain, and multiple NPXY sequences. The encoded protein is localized in the nucleus and cytoplasm. It binds to integrin cytoplasmic domain-associated protein-1 alpha (ICAP1alpha), and plays a critical role in beta1-integrin-mediated cell proliferation. It associates with junction proteins and RAS-related protein 1A (Rap1A), which requires the encoded protein for maintaining the integrity of endothelial junctions. It is also a microtubule-associated protein and may play a role in microtubule targeting. Mutations in this gene result in cerebral cavernous malformations. Multiple alternatively spliced transcript variants have been found for this gene. [provided by RefSeq]. View All» UniProt Summary: SUBUNIT STRUCTURE: Interacts with RAP1A. SUBCELLULAR LOCATION: Membrane; Peripheral membrane protein Probable. TISSUE SPECIFICITY: Low levels in brain. Very weak expression found in heart and muscle. INVOLVEMENT IN DISEASE: Defects in KRIT1 are the cause of cerebral cavernous malformations type 1 (CCM1) [MIM:116860]. Cerebral cavernous malformations (CCMs) are congenital vascular anomalies of the central nervous system that can result in hemorrhagic stroke, seizures, recurrent headaches, and focal neurologic deficits. CCMs have an incidence of 0.1%-0.5% in the general population and usually present clinically during the 3rd to 5th decade of life. The lesions are characterized by grossly enlarged blood vessels consisting of a single layer of endothelium and without any intervening neural tissue, ranging in diameter from a few millimeters to several centimeters. SEQUENCE SIMILARITIES: Contains 4 ANK repeats.Contains 1 FERM domain. View All» Product Name: Anti-KRIT-1, clone 15 View All» Concentration: 1.0 mg/mL View All» Antibody Type: Monoclonal Antibody View All» Qty/Pk: 100 μg View All» Format: Purified View All» Host: Mouse View All»

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