KSHV GPCR (Kaposi's Carcinoma-associated Herpes Virus, KSHV, Human Herpes Virus 8, HHV8)

  • Catalog number
    MBS612573
  • Price
    Please ask
  • Size
    0.1 mg
  • Products_type
    Antibody
  • Products_short_name
    [KSHV GPCR]
  • Products_name_syn
    [Anti -KSHV GPCR (Kaposi's Carcinoma-associated Herpes Virus, KSHV, Human Herpes Virus 8, HHV8)]
  • Clonality
    Polyclonal
  • Reactivity
    Human
  • Specificity
    Recognizes human KSHV GPCR. Reacts with KSHV GPCR expressed in transfected cells by flow cytometry.
  • Purity
    Affinity Purified Purified by Protein A affinity chromatography.
  • Form
    Supplied as a liquid in PBS, 0.1% sodium azide and 40% glycerol.
  • Storage_stability
    May be stored at 4 degree C for short-term only. For long-term storage, store at -20 degree C. Aliquots are stable for at least 12 months at -20 degree C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
  • Tested_application
    Flow Cytometry (FC/FACS)
  • Properties
    Human proteins, cDNA and human recombinants are used in human reactive ELISA kits and to produce anti-human mono and polyclonal antibodies. Modern humans (Homo sapiens, primarily ssp. Homo sapiens sapiens). Depending on the epitopes used human ELISA kits can be cross reactive to many other species. Mainly analyzed are human serum, plasma, urine, saliva, human cell culture supernatants and biological samples.
  • Gene target
  • Gene symbol
    OXER1, HCAR1, GPBAR1, GPER1
  • Short name
    KSHV GPCR (Kaposi's Carcinoma-associated Herpes Virus, KSHV, Herpes Virus 8, HHV8)
  • Host
    Rabbit
  • Isotype
    IgG
  • Species
    Virus, Humans, Viruses
  • Alternative name
    KSHV GPCR (Kaposi's Carcinoma-associated Herpes Virus, KSHV, H. sapiens Herpes Virus 8, HHV8)
  • Tissue
    carcinoma
  • Virus
    herpes, hhv8, kaposi, kshv
Gene info
Gene info
Gene info
Gene info
MeSH Data
  • Name
  • Concept
    Scope note: In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
  • Tree numbers
    • E05.393.620.500
  • Qualifiers
    ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
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