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Hemoglobin C Peptide

Hôte: Synthetic CP Without preservative
Rockland
N° du produit ABIN5624621
N° du produit (Fournisseur): 000-001-gs7
191,40 €
Plus frais de livraison 40,00 € et TVA
50 μg
Destination: France
Envoi sous 5 à 8 jours ouvrables

Aperçu rapide pour Hemoglobin C Peptide (ABIN5624621)

Antigène

Hemoglobin C

Source

Synthetic

Application

Control Peptide (CP)
  • Type de proteíne

    Synthetic

    N° du produit (Fournisseur)

    000-001-gs7

    Fournisseur

    Rockland

    Fonction

    HbC Control Peptide

    Attributs du produit

    HbC Control Peptide, Hemoglobin beta subunit C variant, HbBc, HbC, Sickle Cell Disease (SCD)

    Purification

    Greater than 95% specific peptide

    Pureté

    Greater than 95% specific peptide
  • Indications d'application

    Optional[Flow Cytometry Dilution]: HbC peptide can be used as a control with the HbC 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 C

    Sujet

    Synonyms: HbC Control Peptide, Hemoglobin beta subunit C variant, HbBc, HbC, Sickle Cell Disease (SCD)

    Background: HbC peptide corresponds to the E6K mutant in the amino-terminal portion of hemoglobin beta subunit. Functional 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. Less significant than the SCD-E6V, HbC E6K mutation causes a mild hemolytic anemia. HbC peptide is suitable for use as a control with the HbC antibody. This peptide is ideal for investigators involved in Cardiovascular and developmental biology research.

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