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LCA5L antibody (Biotin)

LCA5L Reactivity: Human, Rat, Mouse WB, IHC (p) Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1405705
  • Target See all LCA5L products
    LCA5L (Leber Congenital Amaurosis 5-Like (LCA5L))
    Reactivity
    • 35
    • 29
    • 23
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Human, Rat, Mouse
    Host
    • 50
    Rabbit
    Clonality
    • 50
    Polyclonal
    Conjugate
    • 13
    • 4
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    This LCA5L antibody is conjugated to Biotin
    Application
    • 35
    • 26
    • 16
    • 13
    • 13
    • 8
    • 3
    • 1
    • 1
    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 LCA5L
    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
    LCA5L (Leber Congenital Amaurosis 5-Like (LCA5L))
    Alternative Name
    LCA5L (LCA5L Products)
    Synonyms
    C21orf13 antibody, 4921526F01Rik antibody, Lcca5l antibody, Leber congenital amaurosis 5-like antibody, LCA5L, lebercilin like antibody, LCA5L antibody, Lca5l antibody
    Background

    Synonyms: C21ORF13, Chromosome 21 open reading frame 13, Lca5l, LCA5L_HUMAN, Leber congenital amaurosis 5 like, Leber congenital amaurosis 5 like protein, Leber congenital amaurosis 5-like protein, Lebercilin-like protein.

    Background: Leber congenital amaurosis (LCA) is one of the most common causes of hereditary blindness or severe visual impairment in infants. Mutations in several genes with diverse functions mapping to two loci have been implicated in LCA causation. These proteins are involved in processes such as photoreceptor development and maintenance, phototransduction, vitamin A metabolism and protein trafficking. LCA5, also known as Lebercilin, is a ciliary protein that is widely expressed during development and localizes to the connecting cilia of photoreceptors and to the microtubules, centrioles and primary cilia of cultured mammalian cells. The Leber congenital amaurosis 5-like protein (LCA5L) is a 670 amino acid protein that belongs to the LCA5 family.

    Gene ID
    150082
    UniProt
    O95447
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