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Dynamin 1-Like antibody

This Rabbit Polyclonal antibody specifically detects Dynamin 1-Like in WB, IHC and IF. It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN6569298

Quick Overview for Dynamin 1-Like antibody (ABIN6569298)

Target

See all Dynamin 1-Like (DNM1L) Antibodies
Dynamin 1-Like (DNM1L)

Reactivity

  • 58
  • 46
  • 30
  • 4
  • 4
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human, Mouse

Host

  • 64
  • 12
Rabbit

Clonality

  • 63
  • 13
Polyclonal

Conjugate

  • 39
  • 5
  • 5
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Dynamin 1-Like antibody is un-conjugated

Application

  • 42
  • 31
  • 22
  • 15
  • 13
  • 13
  • 10
  • 8
  • 7
  • 5
  • 3
  • 2
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purification

    Affinity purification

    Immunogen

    Recombinant protein of human DNM1L

    Isotype

    IgG
  • Application Notes

    WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:200

    Restrictions

    For Research Use only
  • Concentration

    1 mg/mL

    Buffer

    Buffer: PBS with 0.02 % sodium azide, 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.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    Dynamin 1-Like (DNM1L)

    Alternative Name

    DRP1

    Background

    Synonyms: DLP1,dnm1l,DNM1L,Dnm1p/Vps1p-like protein,dnml1,DRP1,DVLP,Dymple,Dynamin 1 like,Dynamin family member proline-rich carboxyl-terminal domain less,Dynamin like protein,Dynamin related protein 1,Dynamin-1-like protein,Dynamin-like protein 4,Dynamin-like protein,Dynamin-like protein IV,Dynamin-related protein 1,DYNIV 11,EMPF,EMPF1,FLJ41912,HdynIV,VPS1

    Background: This gene encodes a member of the dynamin superfamily of GTPases. The encoded protein mediates mitochondrial and peroxisomal division, and is involved in developmentally regulated apoptosis and programmed necrosis. Dysfunction of this gene is implicated in several neurological disorders, including Alzheimer's disease. Mutations in this gene are associated with the autosomal dominant disorder, encephalopathy, lethal, due to defective mitochondrial and peroxisomal fission (EMPF). Alternative splicing results in multiple transcript variants encoding different isoforms.

    Molecular Weight

    Observed_MW: 78-82kDa

    Calculated_MW: 60kDa/78kDa/79kDa/80kDa/81kDa/82kDa/83kDa

    Gene ID

    10059

    UniProt

    O00429
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