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Survival Motor Neuron Domain Containing 1 (SMNDC1) (Middle Region) Peptide

SMNDC1 Reactivité: Humain Hôte: Synthetic BP, WB, IHC
N° du produit ABIN984137

Aperçu rapide pour Survival Motor Neuron Domain Containing 1 (SMNDC1) (Middle Region) Peptide (ABIN984137)

Antigène

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

Origine

Humain

Source

  • 3
Synthetic

Application

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

    Middle Region

    Attributs du produit

    This is a synthetic peptide designed for use in combination with anti-SMNDC1 antibody (Catalog #: ARP40612_P050). It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.

    Purification

    Purified
  • Indications d'application

    Each Investigator should determine their own optimal working dilution for specific applications.

    Restrictions

    For Research Use only
  • Format

    Lyophilized

    Reconstitution

    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.

    Concentration

    1 mg/mL

    Buffer

    Final peptide concentration is 1 mg/mL in PBS.

    Conseil sur la manipulation

    Avoid repeated freeze-thaw cycles.

    Stock

    -20 °C

    Stockage commentaire

    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène

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

    Sujet

    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. The protein encoded by this gene 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.

    Alias Symbols: SMNR, SPF30

    Protein Interaction Partner: KPNB1,SNRNP200,SNRPB,CDK5RAP3,DDX21,EWSR1,FDFT1,PPAN,RNMTL1,RPL3,RUVBL1,SF3A2,SF3A3,SF3B1,SF3B2,SF3B3,SF3B4,SNRNP200,TSR1,mad2

    Protein Size: 238

    Poids moléculaire

    27 kDa

    ID gène

    10285

    NCBI Accession

    NM_005871, NP_005862

    UniProt

    O75940
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