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NEK8 antibody (C-Term)

This anti-NEK8 antibody is a Rabbit Polyclonal antibody detecting NEK8 in WB. Suitable for Human.
Catalog No. ABIN391137

Quick Overview for NEK8 antibody (C-Term) (ABIN391137)

Target

See all NEK8 Antibodies
NEK8 (NIMA-Related Kinase 8 (NEK8))

Reactivity

  • 52
  • 17
  • 9
Human

Host

  • 50
  • 2
Rabbit

Clonality

  • 52
Polyclonal

Conjugate

  • 16
  • 5
  • 4
  • 4
  • 3
  • 3
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This NEK8 antibody is un-conjugated

Application

  • 28
  • 24
  • 13
  • 13
  • 3
  • 3
  • 3
  • 1
  • 1
Western Blotting (WB)

Clone

RB5458
  • Binding Specificity

    • 15
    • 8
    • 7
    • 6
    • 3
    • 2
    • 2
    • 2
    • 1
    • 1
    AA 573-604, C-Term

    Purification

    This antibody is prepared by Saturated Ammonium Sulfate (SAS) precipitation followed by dialysis against PBS.

    Immunogen

    This NEK8 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 573-604 amino acids from the C-terminal region of human NEK8.

    Isotype

    Ig Fraction
  • Application Notes

    WB: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    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

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    NEK8 (NIMA-Related Kinase 8 (NEK8))

    Alternative Name

    NEK8

    Background

    NEK8 is a member of the serine/threionine protein kinase family related to NIMA (never in mitosis, gene A) of Aspergillus nidulans. The encoded protein may play a role in cell cycle progression from G2 to M phase. Mutations in the related mouse gene are associated with a disease phenotype that closely parallels the juvenile autosomal recessive form of polycystic kidney disease in humans.

    Molecular Weight

    74806

    Gene ID

    284086

    NCBI Accession

    NP_835464

    UniProt

    Q86SG6
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