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IQCA1 antibody (Biotin)

IQCA1 Reactivity: Human, Mouse, Rat WB, IHC (p) Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1400377
  • Target See all IQCA1 Antibodies
    IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))
    Reactivity
    Human, Mouse, Rat
    Host
    • 32
    • 1
    Rabbit
    Clonality
    • 32
    Polyclonal
    Conjugate
    • 10
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This IQCA1 antibody is conjugated to Biotin
    Application
    • 32
    • 15
    • 14
    • 13
    • 5
    • 1
    • 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 IQCA1
    Isotype
    IgG
    Top Product
    Discover our top product IQCA1 Primary Antibody
  • 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
    IQCA1 (IQ Motif Containing with AAA Domain 1 (IQCA1))
    Alternative Name
    IQCA1 (IQCA1 Products)
    Synonyms
    4930465P12Rik antibody, 4930585L22Rik antibody, BB288505 antibody, Iqca1 antibody, IQCA antibody, RGD1305311 antibody, IQ motif containing with AAA domain antibody, IQ motif containing with AAA domain 1 antibody, Iqca antibody, IQCA1 antibody, Iqca1 antibody
    Background

    Synonyms: IQ and AAA domain-containing protein 1, IQ mot containing with AAA domain 1, IQCA, Iqca1, IQCA1_HUMAN, RGD1305311, FLJ22527, 4930465P12Rik, FLJ33588.

    Background: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

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