RECQL2 anticorps (Middle Region, Thr802)

N° du produit ABIN955584

Cet anticorps anti-RECQL2 Polyclonal Lapin (ABIN955584) détecte spécifiquement RECQL2 dans WB, FACS et EIA. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour RECQL2 anticorps (Middle Region, Thr802) (ABIN955584)

Antigène: RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RECQL2 est non-conjugé

Application: Western Blotting (WB), Flow Cytometry (FACS), Enzyme Immunoassay (EIA)

Détail du produit anti-RECQL2 anticorps

Épitope: AA 794-825, Middle Region, Thr802

Specificité: This antibody detects WRN (Center).

Réactivité croisée (Details): Species reactivity (tested):Human

Purification: Protein A column; followed by peptide affinity purification

Immunogène: KLH conjugated synthetic peptide between 794-825 (T802 amino acids from the Central region of human WRN

Isotype: Ig Fraction

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: 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.

Conseil sur la manipulation: Avoid repeated freezing and thawing.

Stock: 4 °C/-20 °C

Stockage commentaire: Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.

Détails sur RECQL2

Antigène: RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))

Autre désignation: WRN

Sujet: This gene encodes a member of the RecQ subfamily and the DEAH (Asp-Glu-Ala-His) subfamily of DNA and RNA helicases. DNA helicases are involved in many aspects of DNA metabolism, including transcription, replication, recombination, and repair. This protein contains a nuclear localization signal in the C-terminus and shows a predominant nucleolar localization. It possesses an intrinsic 3' to 5' DNA helicase activity, and is also a 3' to 5' exonuclease. Based on interactions between this protein and Ku70/80 heterodimer in DNA end processing, this protein may be involved in the repair of double strand DNA breaks. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by premature aging.Synonyms: DNA helicase, Exonuclease WRN, RECQ3, RECQL2, RecQ protein-like 2, RecQ-like type 3, RecQ3, Werner syndrome ATP-dependent helicase

ID gène: 7486

NCBI Accession: NP_000544

Pathways: Réparation de l'ADN