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C6orf192 antibody (AA 50-80) (Biotin)

C6orf192 Reactivity: Human, Mouse, Rat WB, IHC (p) Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1403257
  • Target See all C6orf192 Antibodies
    C6orf192 (Chromosome 6 Open Reading Frame 192 (C6orf192))
    Binding Specificity
    AA 50-80
    Reactivity
    • 19
    • 18
    • 18
    • 4
    • 4
    • 4
    Human, Mouse, Rat
    Host
    • 19
    Rabbit
    Clonality
    • 19
    Polyclonal
    Conjugate
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This C6orf192 antibody is conjugated to Biotin
    Application
    • 19
    • 13
    • 2
    • 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 C6orf192
    Isotype
    IgG
    Top Product
    Discover our top product C6orf192 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
    C6orf192 (Chromosome 6 Open Reading Frame 192 (C6orf192))
    Alternative Name
    C6orf192 (C6orf192 Products)
    Synonyms
    C3H6orf192 antibody, SLC18B1 antibody, C6orf192 antibody, dJ55C23.6 antibody, 1110021L09Rik antibody, solute carrier family 18, subfamily B, member 1 antibody, solute carrier family 18 member B1 antibody, slc18b1 antibody, SLC18B1 antibody, Slc18b1 antibody
    Background

    Synonyms: C6orf192, dJ55C23.6, MFS-type transporter SLC18B1, Solute carrier family 18 member B1, SLC18B1

    Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf192 gene product has been provisionally designated C6orf192 pending further characterization.

    Gene ID
    116843
    UniProt
    Q6NT16
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