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U-2 OS (human osterogenic sarcoma) Nuclear extract lysate, Non-denatured, Abnova

Product Code. 16069565
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Quantity:
50 μg
Unit Size:
50µg
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Product Code. 16069565 Supplier Abnova Supplier No. L022V4.50ug

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Description

Non-denatured nuclear extract lysate of U-2 OS (human osterogenic sarcoma)

  • Tissue: Bone
  • Host: Human
  • Lysis Buffer:
    • 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, 0.2mM EDTA, 0.5mM DTT and 0.5mM PMSF
    • Buffer D: 20mM HEPES pH 7.9, 20%(v/v) glycerol, 50mM KCl, 0.2mM EDTA, 0.5mM DTT and 0.5mM PMSF
  • Storage buffer: In buffer D

Applications:

Western Blotting, Immunoprecipitation

Specifications

For Use With (Application) Immunoprecipitation, Western Blot
Tissue Bone
Description Nuclear extract cell lysate (non-denatured)
Lysis Buffer 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.
Preparation Method 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.
Quality Control Testing 12.5% SDS-PAGE Stained with Coomassie Blue.
Quantity 50 μg
Storage Buffer In Buffer D.
Host Species Human
Concentration 2.5 mg/mL
Content And Storage Store at -80°C. Aliquot to avoid repeated freezing and thawing.
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