RECQL2 anticorps (AA 787-816)
Aperçu rapide pour RECQL2 anticorps (AA 787-816) (ABIN656017)
Antigène
Voir toutes RECQL2 (WRN) AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
Clone
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Épitope
- AA 787-816
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Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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Immunogène
- This WRN antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 787-816 amino acids from the Central region of human WRN.
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Isotype
- Ig Fraction
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Indications d'application
- WB: 1:1000. IHC-P: 1:100. FC: 1:10~50
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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Date de péremption
- 6 months
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: "miR-200c-3p spreads invasive capacity in human oral squamous cell carcinoma microenvironment." dans: Molecular carcinogenesis, Vol. 57, Issue 2, pp. 295-302, (2018) (PubMed).
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- RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))
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Autre désignation
- WRN
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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.
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Poids moléculaire
- 162461
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ID gène
- 7486
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NCBI Accession
- NP_000544
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UniProt
- Q14191
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Pathways
- Réparation de l'ADN
Antigène
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