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SMNDC1 antibody (N-Term)

This anti-SMNDC1 antibody is a Rabbit Polyclonal antibody detecting SMNDC1 in WB and FACS. Suitable for Human and Mouse.
Catalog No. ABIN653319

Quick Overview for SMNDC1 antibody (N-Term) (ABIN653319)

Target

See all SMNDC1 Antibodies
SMNDC1 (Survival Motor Neuron Domain Containing 1 (SMNDC1))

Reactivity

  • 38
  • 25
  • 16
  • 5
  • 5
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 34
  • 5
Rabbit

Clonality

  • 36
  • 3
Polyclonal

Conjugate

  • 23
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SMNDC1 antibody is un-conjugated

Application

  • 22
  • 15
  • 10
  • 6
  • 6
  • 6
  • 2
  • 1
  • 1
Western Blotting (WB), Flow Cytometry (FACS)

Clone

RB17335
  • Binding Specificity

    • 10
    • 6
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    AA 11-41, N-Term

    Predicted Reactivity

    B, Rat

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This SMNDC1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 11-41 amino acids from the N-terminal region of human SMNDC1.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000. FC: 1:10~50

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

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

    Alternative Name

    SMNDC1

    Background

    This protein 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 protein is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene.

    Molecular Weight

    26711

    Gene ID

    10285

    NCBI Accession

    NP_005862

    UniProt

    O75940
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