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

NHLRC1 antibody

NHLRC1 Reactivity: Human, Rat, Mouse IHC, IF Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7262557
  • Target See all NHLRC1 Antibodies
    NHLRC1 (NHL Repeat Containing 1 (NHLRC1))
    Reactivity
    • 18
    • 3
    • 1
    • 1
    Human, Rat, Mouse
    Host
    • 16
    • 3
    Rabbit
    Clonality
    • 16
    • 3
    Polyclonal
    Conjugate
    • 10
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This NHLRC1 antibody is un-conjugated
    Application
    • 9
    • 9
    • 4
    • 1
    • 1
    • 1
    • 1
    • 1
    Immunohistochemistry (IHC), Immunofluorescence (IF)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human NHLRC1 (NP_940988.2).
    Isotype
    IgG
    Top Product
    Discover our top product NHLRC1 Primary Antibody
  • Application Notes
    IHC 1:50-1:200 IF 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    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
    NHLRC1 (NHL Repeat Containing 1 (NHLRC1))
    Alternative Name
    NHLRC1 (NHLRC1 Products)
    Synonyms
    EPM2A antibody, EPM2B antibody, MALIN antibody, bA204B7.2 antibody, AI505271 antibody, B230309E09Rik antibody, Epm2b antibody, malin-like antibody, NHL repeat containing E3 ubiquitin protein ligase 1 antibody, NHL repeat containing 1 antibody, NHLRC1 antibody, Nhlrc1 antibody
    Background
    The protein encoded by this gene is a single subunit E3 ubiquitin ligase. Laforin is polyubiquitinated by the encoded protein. Defects in this intronless gene lead to an accumulation of laforin and onset of Lafora disease, also known as progressive myoclonic epilepsy type 2 (EPM2).
    Gene ID
    378884
    UniProt
    Q6VVB1
You are here:
Support