CFL1/CFL2 (Human) Cell-Based ELISA Kit

Catalog # KA2685

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Size:1 Kit
Price: USD $ 648.00
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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

    CFL1/CFL2 (Human) Cell-Based ELISA Kit is an indirect enzyme-linked immunoassay for qualitative determination of CFL1/CFL2 expression in cultured cells.

    Suitable Sample

    Attached Cell, Loosely Attached Cell, Suspension Cell

    Label

    HRP-conjugated

    Detection Method

    Colorimetric

    Assay Type

    Qualitative

    Reactivity

    Human, Mouse, Rat

    Regulation Status

    For research use only (RUO)

    Storage Instruction

    Store the kit at 4°C.

  • Applications

    Qualitative

  • Gene Info — CFL1

    Entrez GeneID

    1072

    Protein Accession#

    P23528 (Gene ID : 1073);Q9Y281 (Gene ID : 1072)

    Gene Name

    CFL1

    Gene Alias

    CFL

    Gene Description

    cofilin 1 (non-muscle)

    Omim ID

    601442

    Gene Ontology

    Hyperlink

    Gene Summary

    Cofilin is a widely distributed intracellular actin-modulating protein that binds and depolymerizes filamentous F-actin and inhibits the polymerization of monomeric G-actin in a pH-dependent manner. It is involved in the translocation of actin-cofilin complex from cytoplasm to nucleus.[supplied by OMIM

    Other Designations

    -

  • Gene Info — CFL2

    Entrez GeneID

    1073

    Protein Accession#

    P23528 (Gene ID : 1073);Q9Y281 (Gene ID : 1072)

    Gene Name

    CFL2

    Gene Alias

    NEM7

    Gene Description

    cofilin 2 (muscle)

    Omim ID

    601443 610687

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes an intracellular protein that is involved in the regulation of actin-filament dynamics. This protein is a major component of intranuclear and cytoplasmic actin rods. It can bind G- and F-actin in a 1:1 ratio of cofilin to actin, and it reversibly controls actin polymerization and depolymerization in a pH-dependent manner. Mutations in this gene cause nemaline myopathy type 7, a form of congenital myopathy. Alternative splicing results in multiple transcript variants. [provided by RefSeq

    Other Designations

    cofilin 2

  • Interactome
  • Pathway
  • 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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