UBE2A anticorps

N° du produit ABIN7263755

Détail du produit anti-UBE2A anticorps

Antigène: UBE2A (ube2a) (Ubiquitin-Conjugating Enzyme E2A (ube2a))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp UBE2A est non-conjugé

Application: Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human UBE2A (NP_003327.2).

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:100

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur UBE2A

Antigène: UBE2A (ube2a) (Ubiquitin-Conjugating Enzyme E2A (ube2a))

Autre désignation: UBE2A (ube2a Produits)

Synonymes: anticorps BHR6A, anticorps HR6A, anticorps hhr6a, anticorps rad6a, anticorps ubc2, anticorps mp:zf637-2-000771, anticorps si:bz46j2.4, anticorps wu:fa01h11, anticorps HHR6A, anticorps MRXS30, anticorps MRXSN, anticorps RAD6A, anticorps UBC2, anticorps Mhr6a, anticorps ubiquitin conjugating enzyme E2 A, anticorps ubiquitin conjugating enzyme E2 A L homeolog, anticorps ubiquitin-conjugating enzyme E2A (RAD6 homolog), anticorps ubiquitin-conjugating enzyme E2A, anticorps UBE2A, anticorps ube2a.L, anticorps ube2a, anticorps Ube2a

Sujet: The modification of proteins with ubiquitin is an important cellular mechanism for targeting abnormal or short-lived proteins for degradation. Ubiquitination involves at least three classes of enzymes: ubiquitin-activating enzymes, ubiquitin-conjugating enzymes, and ubiquitin-protein ligases. This gene encodes a member of the E2 ubiquitin-conjugating enzyme family. This enzyme is required for post-replicative DNA damage repair, and may play a role in transcriptional regulation. Mutations in this gene are associated with mental retardation. Alternative splicing results in multiple transcript variants.

ID gène: 7319

UniProt: P49459