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ULK2 antibody (AA 693-938)

The Rabbit Polyclonal anti-ULK2 antibody has been validated for WB, IHC and IF. It is suitable to detect ULK2 in samples from Human.
Catalog No. ABIN1886618

Quick Overview for ULK2 antibody (AA 693-938) (ABIN1886618)

Target

See all ULK2 Antibodies
ULK2 (Unc-51 Like Kinase 2 (ULK2))

Reactivity

  • 51
  • 16
  • 7
Human

Host

  • 41
  • 10
Rabbit

Clonality

  • 42
  • 9
Polyclonal

Conjugate

  • 32
  • 5
  • 4
  • 4
  • 3
  • 3
This ULK2 antibody is un-conjugated

Application

  • 40
  • 34
  • 14
  • 7
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 8
    • 7
    • 7
    • 6
    • 5
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 693-938

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 693 and 938 of ULK2
  • Application Notes

    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Immunohistochemistry: 1.50-1.500
    Immunofluorescence: 1.100-1.200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    ULK2 (Unc-51 Like Kinase 2 (ULK2))

    Alternative Name

    ULK2

    Background

    This gene encodes a protein that is similar to a serine/threonine kinase in C.elegans which is involved in axonal elongation.The structure of this protein is similar to the C.elegans protein in that both proteins have an N-terminal kinase domain, a central proline/serine rich (PS) domain, and a C-terminal (C) domain.The gene is located within the Smith-Magenis syndrome region on chromosome 17.Alternatively spliced transcript variants encoding the same protein have been identified.[provided by RefSeq]

    Molecular Weight

    113 kDa

    Gene ID

    9706

    NCBI Accession

    NM_014683, NP_055498

    Pathways

    Regulation of Cell Size, Autophagy
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