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Survival Motor Neuron Domain Containing 1 (SMNDC1) Peptid

SMNDC1 Reaktivität: Säugetier Wirt: Synthetic BP, WB, IHC
Produktnummer ABIN939789

Kurzübersicht für Survival Motor Neuron Domain Containing 1 (SMNDC1) Peptid (ABIN939789)

Target

SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))

Spezies

Säugetier

Quelle

  • 3
Synthetic

Applikation

Blocking Peptide (BP), Western Blotting (WB), Immunohistochemistry (IHC)
  • Protein-Typ

    Synthetic

    Sequenz

    KGQVKRSIFA SPESVTGKVG VGTCGIADKP MTQYQDTSKY NVRHLMPQ

    Produktmerkmale

    A synthetic peptide for use as a blocking control in assays to test for specificity of SMNDC1 antibody,
    Alternative Names: SMNDC1 control peptide, SMNDC1 antibody Blocking Peptide, Anti-SMNDC1 Blocking Peptide, Survival Motor Neuron Domain Containing 1 Blocking Peptide, SMNR Blocking Peptide, SPF30 Blocking Peptide, SMNDC1, SMNDC-1, SMNDC 1, SMNDC-1 Blocking Peptide, SMNDC 1 Blocking Peptide
  • Applikationshinweise

    Optimal conditions should be determined by the investigator

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 100 µL of distilled water for a final peptide concentration is 1 mg/mL.

    Buffer

    PBS

    Handhabung

    Avoid repeated freeze/thaw cycles.

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store at -20 °C long term.
  • Target

    SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))

    Hintergrund

    This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. SMNDC1 is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy.

    Molekulargewicht

    27 kDa
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