Aperçu rapide pour HeLa Cell Nuclear Extract (ABIN964027)
Espèce de la protéine
Application
Lysed Cells
Lysate Type
Lysate Fraction
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Espèce du lysat
- Human Cells
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N° du produit (Fournisseur)
- w09-001-367
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Fournisseur
- Rockland
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Specificité
- The cells were grown in Dulbecco’s medium supplemented with 10% fetal bovine serum. Cells were washed with PBS and then incubated on ice in modified RIPA buffer, containing 150 mM sodium chloride, 50 mM Tris HCl, pH 7.4, 1 mM EDTA, 1.0% NP-40, 0.5% sodium deoxycholic acid , 0.1% SDS and 0.01% (w/v) sodium azide to lyse the cells. Protein integrity was ensured using a cocktail of protease inhibitors with broad specificity for the inhibition of aspartic, cysteine, and serine proteases as well as aminopeptidases (0.1 mM AEBSF HCl, 0.08 µM Aprotinin, 5 µM Bestatin, 1.5 µM E-64, 2 µM Leupeptin Hemisulfate, 1 µM Pepstatin A). Phosphatase inhibitors 1 mM NaF and 1 mM Na3VO4 were also added. Cell debris was removed by centrifugation. Protein concentration was determined by a modified Lowry assay using a commercially available kit. Protein concentration was adjusted to 2 mg/ml and then an equal volume of 2X SDS-PAGE sample buffer was added.
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Attributs du produit
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Cell Line: HeLa - Human epidermoid carcinoma
Induction: None (Control)
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MEIS1 293T Cell Transient Overexpression Lysate(Denatured)
MEIS1 WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
SLC26A2 293T Cell Transient Overexpression Lysate(Denatured)SLC26A2 WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
PTGS2 293T Cell Transient Overexpression Lysate(Denatured)PTGS2 WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
PTGER2 293T Cell Transient Overexpression Lysate(Denatured)PTGER2 WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
PTGS1 293T Cell Transient Overexpression Lysate(Denatured)PTGS1 WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
LSAMP 293T Cell Transient Overexpression Lysate(Denatured)LSAMP WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
MICB 293T Cell Transient Overexpression Lysate(Denatured)MICB WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
HRG 293T Cell Transient Overexpression Lysate(Denatured)HRG WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
HOXB5 293T Cell Transient Overexpression Lysate(Denatured)HOXB5 WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
MGMT 293T Cell Transient Overexpression Lysate(Denatured)MGMT WB Whole Cell Lysate Overexpression Lysate HEK 293T Cells Reactivité: Humain
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Indications d'application
- Ready-to-use nuclear extracts are especially prepared as positive controls for separation by SDS-PAGE and subsequent western blot analysis. Nuclear extracts are supplied in denaturing buffer without dissociating agents. Heat nuclear extract to 95° C for 5 minutes and rapidly cool. If dissociating conditions are desired add reducing agent prior to heating. The recommended loading volume per lane is 10-30 l depending on the size format of your gel.
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Commentaires
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Lysate Fractionation: Nuclear Extract
Lysate Stimulation: Not Stimulated
Lysate Tissue Culture: Tissue Culture -
Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 1.0 mg/mL
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Buffer
- 1X SDS-PAGE Sample Buffer (62.5 mM Tris HCl, 2% SDS, 10% Glycerol and 0.005% bromophenol blue, pH 6.8)
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Conseil sur la manipulation
- Ready-to-use nuclear extracts are especially prepared as positive controls for separation by SDS-PAGE and subsequent western blot analysis. Nuclear extracts are supplied in denaturing buffer without dissociating agents. Heat nuclear extract to 95 °C for 5 minutes and rapidly cool. If dissociating conditions are desired add reducing agent prior to heating. The recommended loading volume per lane is 10-30 µl depending on the size format of your gel.
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Stock
- -80 °C
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Date de péremption
- 3 months
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Sujet
- Ready-to-use nuclear extracts produced are derived from cell lines or tissues using highly refined extraction protocols to ensure exceptionally high quality, protein integrity and lot-to-lot reproducibility. All extracts are tested by SDS-PAGE using 4-20% gradient gels and immunoblot analysis using antibodies to key cell signaling components to confirm the presence of both high molecular weight and low molecular weight proteins.
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