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Hemoglobin A (HbA) Peptid

Wirt: Synthetic CP Without preservative
Rockland
Produktnummer ABIN5624563
Hersteller Produkt- Nr.: 000-001-gs4

Kurzübersicht für Hemoglobin A (HbA) Peptid (ABIN5624563)

Target

Hemoglobin A (HbA)

Quelle

Synthetic

Applikation

Control Peptide (CP)
  • Protein-Typ

    Synthetic

    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)

    Aufreinigung

    Greater than 95% specific peptide

    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

    Synonyms: Hbβ Control Peptide, Hemoglobin beta subunit, HBB, Sickle Cell Disease (SCD)

    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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