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TMEM242 antibody (AA 21-100) (Biotin)

TMEM242 Reactivity: Mouse, Rat IHC (p), ELISA, IHC (fro) Host: Rabbit Polyclonal Biotin
Catalog No. ABIN1701479
  • Target See all TMEM242 products
    TMEM242 (Transmembrane Protein 242 (TMEM242))
    Binding Specificity
    AA 21-100
    Reactivity
    Mouse, Rat
    Host
    • 14
    Rabbit
    Clonality
    • 14
    Polyclonal
    Conjugate
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This TMEM242 antibody is conjugated to Biotin
    Application
    • 13
    • 13
    • 2
    • 2
    • 2
    • 1
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro))
    Cross-Reactivity
    Mouse, Rat
    Predicted Reactivity
    Human,Cow,Sheep,Pig,Horse
    Purification
    Purified by Protein A.
    Immunogen
    KLH conjugated synthetic peptide derived from human C6orf35
    Isotype
    IgG
  • Application Notes
    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
    TMEM242 (Transmembrane Protein 242 (TMEM242))
    Alternative Name
    C6orf35 (TMEM242 Products)
    Synonyms
    C6orf35 antibody, 1110008A10Rik antibody, 2310046K16Rik antibody, 5730437N04Rik antibody, BM033 antibody, transmembrane protein 242 antibody, TMEM242 antibody, Tmem242 antibody
    Background

    Synonyms: BM033, C6orf35, TM242_HUMAN, Chromosome 6 open reading frame 35, UPF0463 transmembrane protein C6orf35.

    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 C6orf35 gene product has been provisionally designated C6orf35 pending further characterization.

    Gene ID
    729515
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