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Hemoglobin A (HbA) Peptide

Hôte: Synthetic CP Without preservative
Rockland
N° du produit ABIN5624563
N° du produit (Fournisseur): 000-001-gs4

Aperçu rapide pour Hemoglobin A (HbA) Peptide (ABIN5624563)

Antigène

Hemoglobin A (HbA)

Source

Synthetic

Application

Control Peptide (CP)
  • Type de proteíne

    Synthetic

    N° du produit (Fournisseur)

    000-001-gs4

    Fournisseur

    Rockland

    Fonction

    Hemoglobin A (beta chain) Control Peptide

    Attributs du produit

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

    Purification

    Greater than 95% specific peptide

    Pureté

    Greater than 95% specific peptide
  • Indications d'application

    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.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Reconstitution Buffer: Restore with deionized water (or equivalent)

    Reconstitution Volume: 50μL

    Concentration

    1.0 mg/mL

    Buffer

    Buffer: None

    Stabilizer: None

    Preservative: None

    Agent conservateur

    Without preservative

    Stock

    4 °C,-20 °C

    Stockage commentaire

    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.

    Date de péremption

    6 months
  • Antigène

    Hemoglobin A (HbA)

    Sujet

    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.

    ID gène

    3043

    NCBI Accession

    NP_000509

    UniProt

    P68871
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