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MCPH1 antibody (N-Term)

This anti-MCPH1 antibody is a Rabbit Polyclonal antibody detecting MCPH1 in WB. Suitable for Human.
Catalog No. ABIN5531653

Quick Overview for MCPH1 antibody (N-Term) (ABIN5531653)

Target

See all MCPH1 Antibodies
MCPH1 (Microcephalin 1 (MCPH1))

Reactivity

  • 38
  • 23
  • 4
  • 1
Human

Host

  • 46
  • 6
  • 1
Rabbit

Clonality

  • 48
  • 5
Polyclonal

Conjugate

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  • 2
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  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This MCPH1 antibody is un-conjugated

Application

  • 44
  • 22
  • 13
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  • 1
Western Blotting (WB)
  • Binding Specificity

    • 15
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    • 1
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    AA 104-133, N-Term

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This MCPH1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 104-133 amino acids from the N-terminal region of human MCPH1.

    Isotype

    Ig Fraction
  • Application Notes

    For WB starting dilution is: 1:1000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Buffer

    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

    Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.
  • Target

    MCPH1 (Microcephalin 1 (MCPH1))

    Alternative Name

    MCPH1

    Background

    This gene encodes a DNA damage response protein. The encoded protein may play a role in G2/M checkpoint arrest via maintenance of inhibitory phosphorylation of cyclin-dependent kinase 1. Mutations in this gene have been associated with primary autosomal recessive microcephaly 1 and premature chromosome condensation syndrome. Alternatively spliced transcript variants have been described.

    Molecular Weight

    93 kDa

    Gene ID

    79648

    UniProt

    Q8NEM0

    Pathways

    Stem Cell Maintenance
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