"/> A-431 (human epidermoid carcinoma) Nuclear extract lysate, No… | B-LABO France

A-431 (human epidermoid carcinoma) Nuclear extract lysate, Non-denatured; Abnova

Réf. : BL-RE-118053Réf. fabricant : 16029545 50 μg
209,00 € HT

Non-denatured nuclear extract lysate of A-431 (human epidermoid carcinoma)

À utiliser avec (application)
Immunoprecipitation, Western Blot
Tissue
Epidermis
Description
Nuclear extract cell lysate (non-denatured)
Tampon de lyse
Buffer A: 10mM HEPES pH 7.9, 1.5mM MgCl2, 10mM KCl, 0.5 mM DTT. Buffer C: 20mM HEPES pH 7.9, 25%(v/v) Glycerol , 0.42M NaCl , 1.5mM MgCl2, 0.2 mM EDTA, 0.5 mM DTT & 0.5 mM PMSF. Buffer D : 20mM HEPES pH 7.9, 20%(v/v) glycerol, 50mM KCl, 0.2 mM EDTA, 0.5 mM DTT & 0.5 mM PMSF.
Méthode de préparation
Nuclear extract was prepared by using a modified protocol of Dignam et al. Cells were Harvested and homogenized in Buffer A, and then centrifugated at 25,000 g for 20 minutes to remove cytoplasm and pellet the nuclei. The pellet was re-suspended in Buffer C, and then the suspensions were centrifuged to collect nuclear extract. The supernatant was dialyzed against Buffer D. The dialysate was then centrifuged, divided into aliquots, and stored at -80°C. The protein concentration was determined by the method of Bradford (Bio-Rad protein assay, microplate standard assay). The lysate was adjusted to 2 mg/ml.
Marque
Abnova

Applications:

Western Blotting, Immunoprecipitation

Caractéristiques principales

  • Tissue: Epidermis
  • Host: Human
  • Lysis Buffer:
  • Buffer A: 10mM HEPES pH 7.9, 1.5mM MgCl2, 10mM KCl, 0.5mM DTT.
  • Buffer C: 20mM HEPES pH 7.9, 25%(v/v) Glycerol , 0.42M NaCl , 1.5mM MgCl2, 0.2mM EDTA, 0.5mM DTT & 0.5mM PMSF
  • Buffer D : 20mM HEPES pH 7.9, 20%(v/v) glycerol, 50mM KCl, 0.2mM EDTA, 0.5mM DTT & 0.5mM PMSF
  • Storage buffer: In buffer D

Caractéristiques techniques

MarqueAbnova
Réf. B-LABOBL-RE-118053
Réf. fabricant16029545
À utiliser avec (application)Immunoprecipitation, Western Blot
TissueEpidermis
Tampon de lyseBuffer A: 10mM HEPES pH 7.9, 1.5mM MgCl2, 10mM KCl, 0.5 mM DTT. Buffer C: 20mM HEPES pH 7.9, 25%(v/v) Glycerol , 0.42M NaCl , 1.5mM MgCl2, 0.2 mM EDTA, 0.5 mM DTT & 0.5 mM PMSF. Buffer D : 20mM HEPES pH 7.9, 20%(v/v) glycerol, 50mM KCl, 0.2 mM EDTA, 0.5 mM DTT & 0.5 mM PMSF.
Méthode de préparationNuclear extract was prepared by using a modified protocol of Dignam et al. Cells were Harvested and homogenized in Buffer A, and then centrifugated at 25,000 g for 20 minutes to remove cytoplasm and pellet the nuclei. The pellet was re-suspended in Buffer C, and then the suspensions were centrifuged to collect nuclear extract. The supernatant was dialyzed against Buffer D. The dialysate was then centrifuged, divided into aliquots, and stored at -80°C. The protein concentration was determined by the method of Bradford (Bio-Rad protein assay, microplate standard assay). The lysate was adjusted to 2 mg/ml.
Test du contrôle qualité12.5% SDS-PAGE Stained with Coomassie Blue.
Quantité50 μg
Tampon de stockageIn Buffer D.
Espèces hôtesHuman
Contenu et stockageStore at -80°C. Aliquot to avoid repeated freezing and thawing.
Une question, une configuration particulière ?
Contactez-nous pour un devis.