Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

GRHL2 antibody (AA 80-250)

GRHL2 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN6141384
  • Target See all GRHL2 Antibodies
    GRHL2 (Grainyhead-Like 2 (GRHL2))
    Binding Specificity
    • 7
    • 6
    • 6
    • 6
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 80-250
    Reactivity
    • 29
    • 6
    • 5
    • 4
    • 4
    • 4
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Host
    • 25
    • 4
    Rabbit
    Clonality
    • 28
    • 1
    Polyclonal
    Conjugate
    • 15
    • 4
    • 3
    • 3
    • 2
    • 2
    This GRHL2 antibody is un-conjugated
    Application
    • 22
    • 19
    • 3
    • 3
    • 2
    Western Blotting (WB)
    Sequence
    LSVSKASDSQ EDQEKRNCLG TSEAQSNLSG GENRVQVLKT VPVNLSLNQD HLENSKREQY SISFPESSAI IPVSGITVVK AEDFTPVFMA PPVHYPRGDG EEQRVVIFEQ TQYDVPSLAT HSAYLKDDQR STPDSTYSES FKDAATEKFR SASVGAEEYM YDQTSSGTFQ Y
    Cross-Reactivity
    Human, Rat
    Characteristics
    Polyclonal Antibodies
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein containing a sequence corresponding to amino acids 80-250 of human GRHL2 (NP_079191.2).
    Isotype
    IgG
    Top Product
    Discover our top product GRHL2 Primary Antibody
  • Application Notes
    WB,1:500 - 1:2000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    GRHL2 (Grainyhead-Like 2 (GRHL2))
    Alternative Name
    GRHL2 (GRHL2 Products)
    Background
    The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28).,GRHL2,BOM,DFNA28,ECTDS,TFCP2L3,Epigenetics & Nuclear Signaling,Transcription Factors,Neuroscience,GRHL2
    Molecular Weight
    69 kDa/71 kDa
    Gene ID
    79977
    UniProt
    Q6ISB3
    Pathways
    Tube Formation
You are here:
Support