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Anti-HYPE/HIP13 Rabbit Polyclonal Antibody
  BOSSBS-11698R
 :  Bioss
Anti-HYPE/HIP13 Rabbit Polyclonal Antibody
  BOSSBS-11698R
 :  Bioss

 

  • Antibody type:
    Primary
  • Antigen name:
    Adenosine monophosphate-protein transferase FICD
  • Antigen symbol:
    HYPE/HIP13
  • Clonality:
    Polyclonal
  • Conjugation:
    Unconjugated
  • Host:
    Rabbit
  • ImmunoChemistry:
    Yes
  • Isotype:
    IgG
  • Reactivity:
    Human,
    Rat,
    Mouse
  • Western blot:
    Yes
  • Form:
    liquid
  • Antigen synonyms:
    Huntingtin-interacting protein 13|Huntingtin interacting protein 13|FICD_HUMAN|AMPylator FICD|ficd|Huntingtin-interacting protein E.|FIC domain containing|HIP13|Huntingtin interacting protein E|Huntingtin yeast partner E|FIC domain-containing protein|Huntingtin interactor protein E|Adenosine monophosphate-protein transferase FICD|FIC domain containing protein|HIP-13|Fic S phase protein cell division homolog
  • Storage buffer:
    Aqueous buffered solution containing 100ug/ml BSA, 50% glycerol and 0,09% sodium azide. Store at -20°C for 12 months.
  • Concentration:
    1 ug/ul
  • Shipping temperature:
    4 °C
  • Purification:
    Purified by Protein A.
  • Size:
    100 μg
  • Pk:
    100 µl

 

 

Huntingtin yeast partner E is a 458 amino acid single-pass membrane protein. HYPE is thought to interact with Huntingtin, a protein which induces neurodegeneration when mutated. HYPE also contains two tetratricopeptide repeats (TPR), which may be involved in protein-protein interaction. The gene that encodes HYPE is located on chromosome 12, which encodes over 1,100 genes within 132 million bases and makes up about 4.5% of the human genome. A number of skeletal deformities are linked to chromosome 12 including hypochondrogenesis, achondrogenesis and Kniest dysplasia. Chromosome 12 is also home to a homeobox gene cluster which encodes crucial transcription factors for morphogenesis, and the natural killer complex gene cluster encoding C-type lectin proteins which mediate the NK cell response to MHC I interaction. Trisomy 12p leads to facial development defects, seizure disorders and a host of other symptoms varying in severity depending on the extent of mosaicism and is most severe in cases of complete trisomy.

WB(1:100-1000), IHC-P(1:100-500), IF(IHC-P)(1:50-200)

Type: Primary
Antigen: HYPE/HIP13
Clonality: Polyclonal
Clone:
Conjugation: Unconjugated
Epitope:
Host: Rabbit
Isotype: IgG
Reactivity: Human, Mouse, Rat