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Rabbit anti-Human MCPH1 Polyclonal Antibody

The antibody against MCPH1 was raised in rabbit using the Recombinant Human Microcephalin protein (536-835AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC, IF.

ADC-44368A

The antibody against MCPH1 was raised in rabbit using the Recombinant Human Microcephalin protein (536-835AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC, IF.

$299.00

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Specifications


Cat.No ADC-44368A ClonalityPolyclonal
Host SpeciesRabbitTarget NameMCPH1
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IF, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Microcephalin protein (536-835AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ8NEM0
Background Information
  • Uniprot Id

    Q8NEM0

  • Target Species

    Human

  • Target Name

    MCPH1

  • Target Full Name

    Microcephalin

  • Target Function

    Implicated in chromosome condensation and DNA damage induced cellular responses. May play a role in neurogenesis and regulation of the size of the cerebral cortex.

  • Target Involvement

    Microcephaly 1, primary, autosomal recessive (MCPH1)

  • Target Subcellular Location

    Cytoplasm, cytoskeleton, microtubule organizing center, centrosome.

  • Target Tissue Specificity

    Expressed in fetal brain, liver and kidney.

  • Target Synonyms

    BRCT repeat inhibitor of TERT expression 1; BRIT 1; FLJ12847; Hypothetical protein FLJ12847; MCPH 1; MCPH1; MCPH1_HUMAN; MCT; Microcephalin 1; Microcephalin; Microcephaly primary autosomal recessive 1

  • Target 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.

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