MCPH1 anticorps (N-Term)

N° du produit ABIN5531653

Détail du produit anti-MCPH1 anticorps

Antigène: MCPH1 (Microcephalin 1 (MCPH1))

Épitope: AA 104-133, N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MCPH1 est non-conjugé

Application: Western Blotting (WB)

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

Immunogène: 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

Information d'application

Indications d'application: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Supplied in PBS with 0.09 % (W/V) sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur MCPH1

Antigène: MCPH1 (Microcephalin 1 (MCPH1))

Autre désignation: MCPH1 (MCPH1 Produits)

Synonymes: anticorps RGD1560642, anticorps MGC83773, anticorps MCPH1, anticorps mct, anticorps brit1, anticorps MGC148665, anticorps BRIT1, anticorps MCT, anticorps 5430437K10Rik, anticorps D030046N04Rik, anticorps microcephalin 1, anticorps microcephalin 1 S homeolog, anticorps microcephaly, primary autosomal recessive 1, anticorps Mcph1, anticorps mcph1.S, anticorps MCPH1, anticorps mcph1

Sujet: 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.

Poids moléculaire: 93 kDa

ID gène: 79648

UniProt: Q8NEM0

Pathways: Stem Cell Maintenance