FBLN5 recombinant monoclonal antibody, clone R07-4B4

Catalog # RAB06425

Size

Price

Stock

Quantity

Size:100 uL
Price: USD $ 531.00
Stock:
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Rabbit recombinant monoclonal antibody raised against humanand mouse FBLN5.Recombinant Antibody,Recombinant Antibodies,Recombinant Monoclonal Antibody,RecomAb,Recombinant Ab,Recombinant Monoclonal Antibodies,Recombinant Abs

    Antibody Species

    Rabbit

    Immunogen

    Original antibody is raised against protein corresponding to full length human FBLN5.

    Theoretical MW (kDa)

    Calculated MW: 50 kD

    Reactivity

    Human, Mouse

    Form

    Liquid

    Purification

    Affinity chromatography

    Isotype

    IgG

    Recommend Usage

    Western Blot (1:500-1:1000)
    The optimal working dilution should be determined by the end use.

    Storage Buffer

    In PBS, 150mM NaCl, pH 7.4 (50% glycerol and 0.02% sodium azide)

    Storage Instruction

    Store at 4°C. For long term storage store at -20°C.
    Aliquot to avoid repeated freezing and thawing.

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Western Blot

  • Gene Info — FBLN5

    Entrez GeneID

    10516

    Protein Accession#

    Q9UBX5

    Gene Name

    FBLN5

    Gene Alias

    ARMD3, DANCE, EVEC, FIBL-5, FLJ90059, UP50

    Gene Description

    fibulin 5

    Omim ID

    123700 219100 604580 608895

    Gene Ontology

    Hyperlink

    Gene Summary

    The protein encoded by this gene is a secreted, extracellular matrix protein containing an Arg-Gly-Asp (RGD) motif and calcium-binding EGF-like domains. It promotes adhesion of endothelial cells through interaction of integrins and the RGD motif. It is prominently expressed in developing arteries but less so in adult vessels. However, its expression is reinduced in balloon-injured vessels and atherosclerotic lesions, notably in intimal vascular smooth muscle cells and endothelial cells. Therefore, the protein encoded by this gene may play a role in vascular development and remodeling. Defects in this gene are a cause of autosomal dominant cutis laxa, autosomal recessive cutis laxa type I (CL type I), and age-related macular degeneration type 3 (ARMD3). [provided by RefSeq

    Other Designations

    developmental arteries and neural crest epidermal growth factor-like|urine p50 protein

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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