DFNA5 purified MaxPab mouse polyclonal antibody (B01P)

Catalog # H00001687-B01P

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Size:50 ug
Price: USD $ 335.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
Western Blot (Transfected lysate)
Application

Western Blot (Transfected lysate)

Western Blot analysis of DFNA5 expression in transfected 293T cell line (H00001687-T01) by DFNA5 MaxPab polyclonal antibody.

Lane 1: DFNA5 transfected lysate(32.56 KDa).
Lane 2: Non-transfected lysate.

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a full-length human DFNA5 protein.MaxPab Polyclonal Antibody,MaxPab Polyclonal Antibodies,MaxPab,DNA Immune,DNA Immunization,Immune Technology

    Immunogen

    DFNA5 (-, 1 a.a. ~ 295 a.a) full-length human protein.

    Sequence

    MQKCVISEHMQVEEKCGGIVGIQTKTVQVSATEDGNVTKDSNVVLEIPAATTIAYGVIELYVKLDGQFEFCLLRGKQGGFENKKRIDPVYLDPLVFREFAFIDMPDAAHGISSQDGPLSVLKQATLLLERNFHPFAELPEPQQTALSDIFQAVLFDDELLMVLEPVCDDLVSGLSPTVAVLGELKPRQQQDLVAFLQLVGCSLQGGCPGPEDAGSKQLFMTAYFLVSALAEMPDSAAALLGTCCKLQIIPTLCHLLRALSDDGVSDLEDPTLTPLKDTERFGIVQRLFASADISL

    Host

    Mouse

    Reactivity

    Human

    Quality Control Testing

    Antibody reactive against mammalian transfected lysate.

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Transfected lysate)

    Western Blot analysis of DFNA5 expression in transfected 293T cell line (H00001687-T01) by DFNA5 MaxPab polyclonal antibody.

    Lane 1: DFNA5 transfected lysate(32.56 KDa).
    Lane 2: Non-transfected lysate.
  • Gene Info — DFNA5

    Entrez GeneID

    1687

    GeneBank Accession#

    BC019689

    Protein Accession#

    -

    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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