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Anti-C1ORF111 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Anti-C1ORF111 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Catalog # BOSSBS-15007R-FITC
Supplier:  Bioss
Anti-C1ORF111 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
Catalog # BOSSBS-15007R-FITC
Supplier:  Bioss

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Specifications

  • Antibody type:
    Primary
  • Antigen name:
    C1ORF111
  • Clonality:
    Polyclonal
  • Conjugation:
    FITC (Fluorescein Isothiocyanate)
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Isotype:
    IgG
  • Western blot:
    Yes
  • Epitope:
    31-130/261
  • Form:
    Liquid
  • Gene ID:
    284680
  • Antigen synonyms:
    RP11-565P22.3|CA111_HUMAN|hypothetical protein LOC284680|chromosome 1 open reading frame 111|HSD20
  • Modification:
    Unmodified
  • Storage buffer:
    Aqueous buffered solution containing 0,01M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol.
  • Molecular weight:
    29 kDa
  • Storage temperature:
    Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
  • Concentration:
    1 µg/µl
  • Shipping temperature:
    4 °C
  • Immunogen:
    KLH conjugated synthetic peptide derived from human C1ORF111
  • Tested applications:
    ICC
  • Purification:
    Purified by Protein A
  • Pack type:
    Vial
  • Pk:
    100 µl

Specifications

About this item

Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf111 gene product has been provisionally designated C1orf111 pending further characterization.

Type: Primary
Antigen: C1ORF111
Clonality: Polyclonal
Clone:
Conjugation: FITC
Public Immunogen Range: 31-130/261
Host: Rabbit
Isotype: IgG
Reactivity: