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LURAP1L antibody (Biotin)

LURAP1L Reactivity: Human, Mouse, Rat WB, IHC (p) Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1403059
  • Target See all LURAP1L products
    LURAP1L (Leucine Rich Adaptor Protein 1-Like (LURAP1L))
    Reactivity
    Human, Mouse, Rat
    Host
    • 21
    Rabbit
    Clonality
    • 21
    Polyclonal
    Conjugate
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This LURAP1L antibody is conjugated to Biotin
    Application
    • 21
    • 13
    • 7
    • 7
    • 6
    • 3
    Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Cross-Reactivity
    Human, Mouse, Rat
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C9orf150
    Isotype
    IgG
  • Application Notes
    WB 1:300-5000
    IHC-P 1:200-400
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
    Preservative
    ProClin
    Precaution of Use
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Storage
    -20 °C
    Storage Comment
    Store at -20°C for 12 months.
    Expiry Date
    12 months
  • Target
    LURAP1L (Leucine Rich Adaptor Protein 1-Like (LURAP1L))
    Alternative Name
    C9orf150 (LURAP1L Products)
    Synonyms
    C9orf150 antibody, bA3L8.2 antibody, RGD1308059 antibody, 1110029A09Rik antibody, AV077978 antibody, AV175137 antibody, D4Bwg0951e antibody, WI-13707 antibody, bM350F23.1 antibody, leucine rich adaptor protein 1 like antibody, leucine rich adaptor protein 1-like antibody, LURAP1L antibody, Lurap1l antibody
    Background

    Synonyms: LURAP1L, bA3L8.2, FLJ38505, C9orf150, Chromosome 9 open reading frame 150, CI150_HUMAN, FLJ90271, HYST0841, MGC46502, Uncharacterized protein C9orf150.

    Background: C9orf150 is a 231 amino acid protein encoded by a gene that maps to human chromosome 9p23. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

    Gene ID
    286343
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