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SMN1 antibody

This Mouse Monoclonal antibody specifically detects SMN1 in WB, ELISA and IF. It exhibits reactivity toward Human, Mouse and Rat.
Catalog No. ABIN7119175

Quick Overview for SMN1 antibody (ABIN7119175)

Target

See all SMN1 Antibodies
SMN1 (Survival of Motor Neuron 1, Telomeric (SMN1))

Reactivity

  • 60
  • 33
  • 15
  • 6
  • 6
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 64
  • 11
Mouse

Clonality

  • 55
  • 20
Monoclonal

Conjugate

  • 37
  • 5
  • 4
  • 3
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SMN1 antibody is un-conjugated

Application

  • 56
  • 27
  • 15
  • 13
  • 13
  • 12
  • 11
  • 8
  • 8
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF)

Clone

3D2
  • Purpose

    SMN1 antibody

    Purification

    Protein A+G purification

    Purity

    ≥95 % as determined by SDS-PAGE

    Immunogen

    survival of motor neuron 2, centromeric

    Isotype

    IgG1
  • Application Notes

    WB: 1:1000-1:6000, IF: 1:50-1:500

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

    Preservative

    Sodium azide

    Precaution of Use

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

    Handling Advice

    Avoid repeated freeze / thaw cycles.

    Storage

    -20 °C

    Storage Comment

    -20°C for 12 months

    Expiry Date

    12 months
  • Target

    SMN1 (Survival of Motor Neuron 1, Telomeric (SMN1))

    Alternative Name

    SMN1

    Background

    Synonyms: Survival motor neuron protein|Component of gems 1|Gemin-1|SMN1|SMN|SMNT

    Background: The survival of motor neurons(SMN) genes are the disease genes of spinal muscular atrophy(SMA), a common motor neuron degenerative disease. The level of SMN protein correlates with phenotypic severity of SMA. SMA patients lack a functional SMN1 gene, but they possess an intact SMN2 gene, which though nearly identical to SMN1, is only partially functional, because a large majority of SMN2 transcripts lack exon 7, resulting in production of a truncated, less stable SMN protein. This antibody can recognize human,mouse and rat SMN.

    Molecular Weight

    38 kDa

    UniProt

    Q16637

    Pathways

    Ribonucleoprotein Complex Subunit Organization
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