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SCN2B Protein (His tag)

SCN2B Origin: Human Host: Escherichia coli (E. coli) Recombinant > 80 % as determined by SDS-PAGE and Coomassie blue staining AbP, STD
Catalog No. ABIN2731491
  • Target See all SCN2B Proteins
    SCN2B (Sodium Channel, Voltage-Gated, Type II, beta (SCN2B))
    Protein Type
    Recombinant
    Origin
    • 3
    • 2
    • 1
    • 1
    Human
    Source
    • 4
    • 2
    • 1
    Escherichia coli (E. coli)
    Purification tag / Conjugate
    This SCN2B protein is labelled with His tag.
    Application
    Antibody Production (AbP), Standard (STD)
    Characteristics
    • Recombinant human SCN2B (full length, N-term HIS tag) protein expressed in E. coli.
    • Produced with end-sequenced ORF clone
    Purity
    > 80 % as determined by SDS-PAGE and Coomassie blue staining
    Top Product
    Discover our top product SCN2B Protein
  • Application Notes
    Recombinant human proteins can be used for:
    Native antigens for optimized antibody production
    Positive controls in ELISA and other antibody assays
    Comment

    The tag is located at the N-terminal.

    Restrictions
    For Research Use only
  • Concentration
    50 μg/mL
    Buffer
    25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.
    Storage
    -80 °C
    Storage Comment
    Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
  • Target
    SCN2B (Sodium Channel, Voltage-Gated, Type II, beta (SCN2B))
    Alternative Name
    Scn2b (SCN2B Products)
    Synonyms
    SCNB2 Protein, 2810451E09Rik Protein, AI840361 Protein, Gm183 Protein, SCN2B Protein, sodium voltage-gated channel beta subunit 2 Protein, sodium channel, voltage-gated, type II, beta Protein, sodium voltage-gated channel beta subunit 2 L homeolog Protein, SCN2B Protein, Scn2b Protein, scn2b.L Protein, scn2b Protein
    Background
    The protein encoded by this gene is the beta 2 subunit of the type II voltage-gated sodium channel. The encoded protein is involved in cell-cell adhesion and cell migration. Defects in this gene can be a cause of Brugada Syndrome, atrial fibrillation, or sudden infant death syndrome.
    Molecular Weight
    24.1 kDa
    NCBI Accession
    NP_004579
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