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KLC2 antibody (AA 1-90)

This Rabbit Polyclonal antibody specifically detects KLC2 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN7268140

Quick Overview for KLC2 antibody (AA 1-90) (ABIN7268140)

Target

See all KLC2 Antibodies
KLC2 (Kinesin Light Chain 2 (KLC2))

Reactivity

  • 47
  • 19
  • 15
  • 15
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 45
  • 2
Rabbit

Clonality

  • 47
Polyclonal

Conjugate

  • 17
  • 3
  • 3
  • 3
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This KLC2 antibody is un-conjugated

Application

  • 40
  • 20
  • 19
  • 19
  • 13
  • 13
  • 8
  • 3
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
    • 8
    • 8
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    AA 1-90

    Purpose

    KLC2 Rabbit pAb

    Sequence

    MAMMVFPREE KLSQDEIVLG TKAVIQGLET LRGEHRALLA PLVAPEAGEA EPGSQERCIL LRRSLEAIEL GLGEAQVILA LSSHLGAVES

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-90 of human KLC2 (NP_073733.1).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000

    Restrictions

    For Research Use only
  • Format

    Liquid

    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

    KLC2 (Kinesin Light Chain 2 (KLC2))

    Alternative Name

    KLC2

    Background

    The protein encoded by this gene is a light chain of kinesin, a molecular motor responsible for moving vesicles and organelles along microtubules. Defects in this gene are a cause of spastic paraplegia, optic atrophy, and neuropathy (SPOAN) syndrome. [provided by RefSeq, Mar 2016],KLC2,SPOAN,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,KLC2

    Molecular Weight

    60kDa/68kDa

    Gene ID

    64837

    UniProt

    Q9H0B6
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