GSDME recombinant monoclonal antibody, clone R09-7C1

Catalog # RAB02325

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
Images
Western Blot
Application

Western Blot

Western Blot analysis of A549 lysates with GSDME recombinant monoclonal antibody, clone R09-7C1 (Cat # RAB02325).

  • Specification

    Product Description

    Rabbit recombinant monoclonal antibody raised against human GSDME.Recombinant Antibody,Recombinant Antibodies,Recombinant Monoclonal Antibody,RecomAb,Recombinant Ab,Recombinant Monoclonal Antibodies,Recombinant Abs

    Antibody Species

    Rabbit

    Immunogen

    Original antibody is raised against recombinant protein corresponding to human GSDME.

    Theoretical MW (kDa)

    Calculated MW: 55 kD

    Reactivity

    Human

    Form

    Liquid

    Purification

    Affinity purification

    Isotype

    IgG

    Recommend Usage

    Immunoprecipitation (1:20)
    Western Blot (1:500-1:1000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 50 mM Tris-Glycine, pH 7.4 (0.15 M NaCl, 40% Glycerol, 0.01% Sodium azide and 0.05% BSA)

    Storage Instruction

    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

    Western Blot analysis of A549 lysates with GSDME recombinant monoclonal antibody, clone R09-7C1 (Cat # RAB02325).

    Immunoprecipitation

  • Gene Info — DFNA5

    Entrez GeneID

    1687

    Protein Accession#

    O60443

    Gene Name

    DFNA5

    Gene Alias

    ICERE-1

    Gene Description

    deafness, autosomal dominant 5

    Omim ID

    600994 608798

    Gene Ontology

    Hyperlink

    Gene Summary

    Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq

    Other Designations

    deafness, autosomal dominant 5 protein|inversely correlated with estrogen receptor expression 1|nonsyndromic hearing impairment 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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