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LRRC57 antibody

LRRC57 Reactivity: Human, Mouse, Rat ELISA, IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7237338
  • Target See all LRRC57 Antibodies
    LRRC57 (Leucine Rich Repeat Containing 57 (LRRC57))
    Reactivity
    • 33
    • 7
    • 5
    • 4
    • 4
    • 4
    • 3
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 32
    • 1
    Rabbit
    Clonality
    • 33
    Polyclonal
    Conjugate
    • 13
    • 4
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This LRRC57 antibody is un-conjugated
    Application
    • 23
    • 18
    • 13
    • 12
    • 2
    • 1
    ELISA, Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant protein of human LRRC57
    Isotype
    IgG
    Top Product
    Discover our top product LRRC57 Primary Antibody
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    0.2 mg/mL
    Buffer
    PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
    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
    LRRC57 (Leucine Rich Repeat Containing 57 (LRRC57))
    Alternative Name
    LRRC57 (LRRC57 Products)
    Synonyms
    zgc:92240 antibody, 2810002D13Rik antibody, AA407405 antibody, RGD1307128 antibody, leucine rich repeat containing 57 antibody, leucine rich repeat containing 57 L homeolog antibody, lrrc57 antibody, lrrc57.L antibody, LRRC57 antibody, Lrrc57 antibody
    Background
    LRRC57 (leucine rich repeat containing 57) is a 239 amino acid protein that contains eight LRR repeats and is encoded by a gene that maps to human chromosome 15q15.2. Chromosome 15 houses over 700 genes and comprises nearly 3 % of the human genome. Angelman syndrome, Prader-Willi syndrome, Tay-Sachs disease and Marfan syndrome are all associated with defects in chromosome 15-localized genes.
    UniProt
    Q8N9N7
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