MSH5 anticorps (AA 525-552)

N° du produit ABIN1538472

Détail du produit anti-MSH5 anticorps

Antigène: MSH5 (MutS Homolog 5 (MSH5))

Épitope: AA 525-552

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MSH5 est non-conjugé

Application: Western Blotting (WB)

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

Immunogène: This MSH5 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 525-552 amino acids from the Central region of human MSH5.

Clone: RB36302

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody 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: MSH5 Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur MSH5

Antigène: MSH5 (MutS Homolog 5 (MSH5))

Autre désignation: MSH5 (MSH5 Produits)

Synonymes: anticorps MSH5, anticorps G7, anticorps MUTSH5, anticorps NG23, anticorps Mut5, anticorps mutS homolog 5, anticorps mutS protein homolog 5, anticorps MSH (MutS Homolog) family, anticorps MSH5, anticorps msh5, anticorps LOC100635155, anticorps Msh5, anticorps msh-5

Sujet: This gene encodes a member of the mutS family of proteins that are involved in DNA mismatch repair and meiotic recombination. This protein is similar to a Saccharomyces cerevisiae protein that participates in segregation fidelity and crossing-over events during meiosis. This protein plays a role in promoting ionizing radiation-induced apoptosis. This protein forms heterooligomers with another member of this family, mutS homolog 4. Polymorphisms in this gene have been linked to various human diseases, including IgA deficiency, common variable immunodeficiency, and premature ovarian failure. Alternative splicing results multiple transcript variants.

Poids moléculaire: 92875

ID gène: 4439

NCBI Accession: NP_002432, NP_079535, NP_751897, NP_751898

UniProt: O43196

Pathways: M Phase