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CACFD1 antibody (AA 41-130) (Biotin)

CACFD1 Reactivity: Human WB, ELISA, IHC (fro), IHC (p) Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1701106
  • Target See all CACFD1 products
    CACFD1 (Calcium Channel Flower Domain Containing 1 (CACFD1))
    Binding Specificity
    • 14
    • 8
    • 7
    • 6
    AA 41-130
    Reactivity
    • 28
    • 8
    Human
    Host
    • 28
    Rabbit
    Clonality
    • 28
    Polyclonal
    Conjugate
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This CACFD1 antibody is conjugated to Biotin
    Application
    • 28
    • 14
    • 13
    • 13
    • 2
    • 2
    • 1
    Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    Predicted Reactivity
    Human,Mouse,Rat,Dog,Pig,Rabbit
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C9orf7
    Isotype
    IgG
  • Application Notes
    WB 1:300-5000
    IHC-P 1:200-400
    IHC-F 1:100-500
    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
    CACFD1 (Calcium Channel Flower Domain Containing 1 (CACFD1))
    Alternative Name
    C9orf7 (CACFD1 Products)
    Synonyms
    C9orf7 antibody, D9S2135 antibody, FLOWER antibody, 5930434B04Rik antibody, mFwe antibody, calcium channel flower domain containing 1 antibody, CACFD1 antibody, Cacfd1 antibody
    Background

    Synonyms: C9orf7, Calcium channel flower homolog, Chromosome 9 open reading frame 7, D9S2135, FLOWR_HUMAN, RP13-100B2.5.

    Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered 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. The C9orf7 gene product has been provisionally designated C9orf7 pending further characterization.

    Gene ID
    11094
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