Merck Millipore代理05-449 Anti-Bin1 Antibody, clone 99D;store at -20℃

2025-06-25

货号:05-449

品牌:Merck Millipore

规格:200Ug

目录价:¥6127.00

市场价格:¥5207.95

会员价格:¥4901.60

金山科研平台,产品价格货期咨询微信:jinshanbio Description: Anti-Bin1 Antibody, clone 99D | 05-449 View All» Replaces: MAB4131 View All» Promotional Text: Special Shipping Offer on Antibodies100% Performance Guaranteed View All» Trade Name: Upstate (Millipore) View All» Specificity: Bin1 View All» Molecular Weight: 56kDa View All» Immunogen: Partial fusion protein corresponding to amino acids 189-398 of human Bin1. Clone 99D View All» Isotype: IgG1κ View All» Species Reactivity:

  • Human

  • Mouse

  • Rat

    View All» Quality Assurance: routinely evaluated by immunoblot on RIPA lysate of C2C12 cells. View All» Purification Method: Protein G chromatography View All» Presentation: 0.1M Tris-glycine, pH 7.4, containing 0.05% sodium azide View All» Storage Conditions: 1 year at -20°C View All» UniProt Number: O00499 View All» Entrez Gene Number: NM_139343 View All» Gene Symbol:
    • BIN1

    • AMPH2

    • amphiphysin-like

    • MGC10367

    • DKFZp547F068

    • AMPHL

    • SH3P9

      View All» Sales Restrictions: Due to license agreement restrictions, this product cannot be purchased for resale. 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:
      • Immunoprecipitation

      • Western Blotting

      • Immunohistochemistry

        View All» Entrez Gene Summary: This gene encodes several isoforms of a nucleocytoplasmic adaptor protein, one of which was initially identified as a MYC-interacting protein with features of a tumor suppressor. Isoforms that are expressed in the central nervous system may be involved in synaptic vesicle endocytosis and may interact with dynanim, synaptojanin, endophilin, and clathrin. Isoforms that are expressed in muscle and ubiquitously expressed isoforms localize to the cytoplasm and nucleus and activate a caspase-independent apoptotic process. Studies in mouse suggest that this gene plays an important role in cardiac muscle development. Alternate splicing of the gene results in ten transcript variants encoding different isoforms. Aberrant splice variants expressed in tumor cell lines have also been described. View All» UniProt Summary: FUNCTION: SwissProt: O00499 # May be involved in regulation of synaptic vesicle endocytosis. May act as a tumor suppressor and inhibits malignant cell transformation.SIZE: 593 amino acids; 64699 Da SUBUNIT: Heterodimer with AMPH. Binds SH3GLB1 (By similarity). Binds to SYNJ1 and DNM1 through its SH3 domain, and to clathrin through a region outside of the SH3 domain. Also binds AP2A2. Interacts with the N-terminal transactivation domain of MYC in a manner requiring the integrity of the conserved MYC box regions 1 and 2. Interacts with BIN2. Interacts with HCV NS5A through its SH3 domain.SUBCELLULAR LOCATION: Isoform BIN1: Nucleus. & Isoform IIA: Cytoplasm.TISSUE SPECIFICITY: Ubiquitous. Highest expression in the brain and muscle. Isoform IIA is expressed only in the brain where it is concentrated in axon initial segments and nodes of Ranvier. Isoform BIN1 is widely expressed with highest expression in skeletal muscle.PTM: Phosphorylated by protein kinase C (By similarity).DISEASE: "SwissProt: O00499 # Defects in BIN1 are the cause of centronuclear myopathy autosomal recessive (ARCNM) [MIM:255200]; also known as autosomal recessive myotubular myopathy. Centronuclear myopathies are congenital muscle disorders characterized by progressive muscular weakness and wasting involving mainly limb girdle, trunk, and neck muscles. It may also affect distal muscles. Weakness may be present during childhood or adolescence or may not become evident until the third decade of life. Ptosis is a frequent clinical feature. The most prominent histopathologic features include high frequency of centrally located nuclei in muscle fibers not secondary to regeneration, radial arrangement of sarcoplasmic strands around the central nuclei, and predominance and hypotrophy of type 1 fibers."SIMILARITY: SwissProt: O00499 ## Contains 1 BAR domain. & Contains 1 SH3 domain. View All» Brand Family: Upstate View All» Product Name: Anti-Bin1 Antibody, clone 99D | 05-449 View All» Antibody Type: Monoclonal Antibody View All» Qty/Pk: 200 µg View All» Format: Purified View All» Host: Mouse View All»

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