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Paired Box 1 (PAX1) Peptide

PAX1 Host: Synthetic CP Without preservative
Rockland
Catalog No. ABIN5624565
Supplier Product No.: 000-001-gs5

Quick Overview for Paired Box 1 (PAX1) Peptide (ABIN5624565)

Target

PAX1 (Paired Box 1 (PAX1))

Source

  • 6
Synthetic

Application

Control Peptide (CP)
  • Peptide Type

    Synthetic

    Supplier Product No.

    000-001-gs5

    Supplier

    Rockland

    Purpose

    HbS Control Peptide

    Characteristics

    HbS Control Peptide, Hemoglobin beta subunit sickle mutant, HBS, HBBs, Sickle Cell Disease (SCD)

    Purification

    Greater than 95% specific peptide

    Purity

    Greater than 95% specific peptide
  • Application Notes

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

    Concentration

    1.0 mg/mL

    Buffer

    Buffer: None

    Stabilizer: None

    Preservative: None

    Preservative

    Without preservative

    Storage

    -20 °C

    Storage Comment

    Store vial at -20 °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.

    Expiry Date

    6 months
  • Target

    PAX1 (Paired Box 1 (PAX1))

    Background

    Synonyms: HbS Control Peptide, Hemoglobin beta subunit sickle mutant, HBS, HBBs, Sickle Cell Disease (SCD)

    Background: HbS peptide corresponds to the E6V mutant in the hemoglobin beta subunit. 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. Hemoglobin S is the predominant hemoglobin in people with sickle cell disease. The alpha chain is normal. The disease-producing mutation exists in the beta chain, giving the molecule the structure, α2βS2. People who have one sickle mutant gene and one normal beta gene have sickle cell trait which is benign. 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. HbS peptide may be used as a control with Anti-HbS antibody. This peptide is ideal for investigators involved in Cardiovascular and developmental biology research.

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