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Anti-C8ORF77 Rabbit Polyclonal Antibody (FITC)
Anti-C8ORF77 Rabbit Polyclonal Antibody (FITC)
Catalog # BOSSBS-15302R-FITC
Supplier:  Bioss
Anti-C8ORF77 Rabbit Polyclonal Antibody (FITC)
Catalog # BOSSBS-15302R-FITC
Supplier:  Bioss

Specifications

  • Antibody type:
    Primary
  • Antigen name:
    C8orf77
  • Clonality:
    Polyclonal
  • Conjugation:
    FITC (Fluorescein Isothiocyanate)
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Isotype:
    IgG
  • Western blot:
    Yes
  • Epitope:
    101-200/211
  • Form:
    Liquid
  • Antigen synonyms:
    Chromosome 8 open reading frame 77|Putative uncharacterized protein C8orf77|ZNFS1_HUMAN|MGC141859
  • Modification:
    Unmodified
  • Storage buffer:
    Aqueous buffered solution containing 0,01 M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol
  • Molecular weight:
    22 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 C8ORF77
  • Tested applications:
    ICC
  • Purification:
    Purified by Protein A
  • Pack type:
    Vial
  • Pk:
    100 µl

Specifications

About this item

C8orf77 (chromosome 8 open reading frame 77) is a 211 amino acid protein encoded by a gene that maps to human chromosome 8q24.3. Consisting of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and are typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome.

Type: Primary
Antigen: C8orf77
Clonality: Polyclonal
Clone:
Conjugation: FITC
Public Immunogen Range: 101-200/211
Host: Rabbit
Isotype: IgG
Reactivity: