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NIH/3T3 (mouse NIH/Swiss embryo) Nuclear extract lysate, Non-denatured; Abnova
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Quantité:
50 μg
Conditionnement:
50µg
Description
Western Blotting, Immunoprecipitation
Spécification
Spécification
| À utiliser avec (application) | Immunoprecipitation, Western Blot |
| Tissue | Embryo, Contact-inhibited |
| 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. |
| Test du contrôle qualité | 12.5% SDS-PAGE Stained with Coomassie Blue. |
| Quantité | 50 μg |
| Tampon de stockage | In Buffer D. |
| Espèces hôtes | Mouse |
| Contenu et stockage | Store at -80°C. Aliquot to avoid repeated freezing and thawing. |
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