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Hemoglobin A (HbA) Peptid

Rockland 000-001-gs4 Wirt: Synthetic CP Without preservative
Rockland
Produktnummer ABIN5624563
Hersteller Produkt- Nr.: 000-001-gs4
  • Target
    Hemoglobin A (HbA)
    Protein-Typ
    Synthetic
    Quelle
    Synthetic
    Applikation
    Control Peptide (CP)
    Hersteller Produkt- Nr.
    000-001-gs4
    Hersteller
    Rockland
    Verwendungszweck
    Hemoglobin A (beta chain) Control Peptide
    Produktmerkmale
    Hbβ Control Peptide, Hemoglobin beta subunit, HBB, Sickle Cell Disease (SCD)
    Reinheit
    Greater than 95% specific peptide
  • Applikationshinweise
    Optional[Flow Cytometry Dilution]: Hemoglobin A (beta chain) peptide can be used as a control with the HbA antibody. Control peptide should be used at 1.0 μg per 1.0 μL of antiserum in per assay.
    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Lyophilized
    Rekonstitution

    Reconstitution Buffer: Restore with deionized water (or equivalent)

    Reconstitution Volume: 50μL

    Konzentration
    1.0 mg/mL
    Buffer

    Buffer: None

    Stabilizer: None

    Preservative: None
    Konservierungsmittel
    Without preservative
    Lagerung
    4 °C,-20 °C
    Informationen zur Lagerung
    Store vial at 2-8 °C prior to opening. Aliquot contents and freeze at -20 °C or below for extended storage. Avoid cycles of freezing and thawing. Centrifuge product if not completely clear after standing at room temperature. Dilute only prior to immediate use.
    Haltbarkeit
    6 months
  • Target
    Hemoglobin A (HbA)
    Hintergrund
    Background: HbA peptide correspond to the hemoglobin beta subunit wild type variant A isoform. Functional adult hemoglobin (Hb) is a hetero tetramer composed of 2 alpha and 2 beta subunits (α2β2). Common isoform variants of hemoglobin include HbA, HbS, HbC, HbF, and HbA2. Sickle cell disease (SCD), thalassemias and hemoglobinopathies occur when aberrant forms of hemoglobin are expressed in children and adults. Globin gene mutations affect the structure and expression levels of Hb. Sickle cell disease and the more benign sickle cell trait are observed in more than 100 million people globally. Perhaps the most significant mutation is the E6V in the beta subunit and the cause of SCD, but other relevant isoforms of Hb are observed. HbA peptide can be used as a control with the HbA antibody. This peptide is ideal for investigators involved in Cardiovascular and developmental biology research.
    Gen-ID
    3043
    NCBI Accession
    NP_000509
    UniProt
    P68871
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