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CMV Pp150 (AA 1011-1048) Protein

Recombinant CMV Pp150-Protein exprimiert in not_set.
Produktnummer ABIN621826
806,40 €
Zzgl. Versandkosten 20,00 € und MwSt
500 μg
Lieferung nach: Deutschland
Lieferung in 10 bis 13 Werktagen

Kurzübersicht für CMV Pp150 (AA 1011-1048) Protein (ABIN621826)

Target

CMV Pp150

Protein-Typ

Recombinant

Spezies

  • 6
  • 3
  • 1
Cytomegalovirus (CMV)

Wirt

Bitte anfragen

Applikation

Western Blotting (WB), ELISA

Reinheit

> 95 % pure as determined by 15 % PAGE (coomassie staining).
  • Proteineigenschaft

    AA 1011-1048

    Spezifität

    Immunoreactive with sera of CMV-infected individuals.

    Produktmerkmale

    Recombinant Cytomegalovirus pp150 (UL32)

    Aufreinigung

    CMV Pp150 was purified by proprietary chromatographic technique.
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  • Applikationshinweise

    CMV Pp65 antigen is suitable for ELISA and Western blots, excellent antigen for detection of CMV with minimal specificity problems.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    25 mM Tris-Hcl pH 8.0, 5 mM EDTA and 50 % glycerol.

    Lagerung

    -20 °C
  • Target

    CMV Pp150

    Substanzklasse

    Viral Protein

    Hintergrund

    The E.Coli derived recombinant protein contains the CMV Pp150 (UL32) immunodominant regions, 1011-1048 amino acids. Introduction: CMV belongs to the Betaherpesvirinae subfamily of Herpesviridae which includes herpes simplex virus types 1 and 2, varicella-zoster virus, and Epstein-Barrvirus. The herpes viruses share a characteristic ability to remain latent over long periods. CMV is a double-stranded linear DNA virus with 162 hexagonal protein capsomeres surrounded by a lipid membrane. CMV has the largest genome of the herpes viruses, ranging from 230-240 kilobase pairs. Human CMV is composed of unique and inverted repeats that include the existence of 4 genome isomers caused by inversion of L-S genome components (class E). Replication may be divided into immediate early, delayed early, and late gene expression based on time of synthesis after infection. The DNA is replicated by rolling circles. In vitro, CMV replicates in human fibroblasts.
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