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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
-15% Promotion 2026
$442.53
$520.62
save $78.09 (-15 %)
Plus shipping costs $50.00
100 μg
Shipping to: United States
Delivery in 13 to 16 Business Days

Quick Overview for SMN1 antibody (ABIN7119175)

Target

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

Reactivity

  • 72
  • 43
  • 25
  • 6
  • 6
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
Human, Mouse, Rat

Host

  • 76
  • 11
Mouse

Clonality

  • 56
  • 31
Monoclonal

Conjugate

  • 41
  • 6
  • 4
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SMN1 antibody is un-conjugated

Application

  • 67
  • 27
  • 24
  • 20
  • 13
  • 13
  • 12
  • 8
  • 8
  • 5
  • 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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