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Anti-C9ORF103 Rabbit Polyclonal Antibody (FITC)
Anti-C9ORF103 Rabbit Polyclonal Antibody (FITC)
Catalog # BOSSBS-15308R-FITC
Supplier:  Bioss
Anti-C9ORF103 Rabbit Polyclonal Antibody (FITC)
Catalog # BOSSBS-15308R-FITC
Supplier:  Bioss

Specifications

  • Antibody type:
    Primary
  • Antigen name:
    C9orf103
  • Clonality:
    Polyclonal
  • Conjugation:
    FITC (Fluorescein Isothiocyanate)
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • ImmunoFluorescence:
    Yes
  • Isotype:
    IgG
  • Western blot:
    Yes
  • Epitope:
    51-150/184
  • Form:
    Liquid
  • Gene ID:
    414328
  • Antigen synonyms:
    OTTHUMP00000021547|Chromosome 9 open reading frame 103|GNTK_HUMAN|C9orf103|Gluconokinase like protein|Probable gluconokinase|Glucokinase like protein|OTTHUMP00000021546|Gluconate kinase|IDNK|RP11-522I20,2|bA522I20,2
  • 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:
    21 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 C9ORF103
  • Tested applications:
    ICC
  • Purification:
    Purified by Protein A
  • Pack type:
    Vial
  • Pk:
    100 µl

Specifications

About this item

C9orf103 (chromosome 9 open reading frame 103), also known as gluconate kinase, is a 187 amino acid protein that belongs to the gluconokinase gntK/gntV family and catalyses the conversion of ATP and D-gluconate to ADP and 6-D-gluconate. Existing as three alternatively spliced isoforms, the gene encoding C9orf103 maps to human chromosome 9q21.32. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought 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 characterised 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.

Type: Primary
Antigen: C9orf103
Clonality: Polyclonal
Clone:
Conjugation: FITC
Public Immunogen Range: 51-150/184
Host: Rabbit
Isotype: IgG
Reactivity: