NE-PER™ Nuclear and Cytoplasmic Extraction Reagents
NE-PER™ Nuclear and Cytoplasmic Extraction Reagents
Thermo Scientific™

NE-PER™ Nuclear and Cytoplasmic Extraction Reagents

The Thermo Scientific NE-PER Nuclear and Cytoplasmic Extraction Kit provides for efficient cell lysis and extraction of separate cytoplasmic andRead more
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Catalog NumberQuantity
7883315 mL
7883575 mL
Catalog number 78833
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15 mL
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The Thermo Scientific NE-PER Nuclear and Cytoplasmic Extraction Kit provides for efficient cell lysis and extraction of separate cytoplasmic and nuclear protein fractions in less than two hours.

Features of the NE-PER Nuclear and Cytoplasmic Extraction Kit:

Fast—obtain nuclear and cytoplasmic fractions of soluble proteins in less than two hours
Proven—the NE-PER Reagent Kit is referenced in more than 950 distinct publications
Versatile – nuclear protein from either cultured cells or tissues (intended for fresh samples only)
Scalable—two kit sizes for producing extracts from cells and tissues
Convenient—simple instructions do not require ultracentrifugation over gradients
Compatible—use for downstream assays, including Western blotting, gel-shift assays, protein assays, reporter gene assays and enzyme activity assays

The NE-PER Kit is a nuclear protein extraction method that involves simple, stepwise lysis of cells and centrifugal isolation of nuclear and cytoplasmic protein fractions. A benchtop microcentrifuge, tubes and pipettors are the only tools required. The NE-PER Reagents efficiently solubilize and separate cytoplasmic and nuclear proteins into fractions with minimal cross-contamination or interference from genomic DNA and mRNA. Once desalted or diluted, the isolated proteins can be used to perform immunoassays and protein interaction experiments, such as mobility shift assays (EMSA), co-immunoprecipitation (Co-IP) and pull-down assays.

There are a variety of methods available to isolate nuclei and prepare nuclear protein extracts. Most of the methods for preparing nuclear extracts are lengthy processes requiring mechanical homogenization, freeze/thaw cycles, extensive centrifugation or dialysis steps that may compromise the integrity of nuclear proteins. The NE-PER Nuclear and Cytoplasmic Extraction Reagent Kit is a reagent-based protocol that enables the stepwise lysis of cells, separation of the cytoplasm from the intact nuclei and then extraction of nuclear proteins away from genomic DNA and mRNA. This gentle process takes less than two hours and requires only a standard bench top centrifuge when using cultured cells. Furthermore, both active nuclear proteins and cytoplasmic proteins can be recovered from the same cell culture or tissue sample.

From two million cells, the kit typically yields 200 to 500 μg cytoplasmic protein and 100 to 200 μg nuclear protein (at a concentration of 1 mg/mL). Typical cross-contamination between cytosolic and nuclear fractions is about 10%. The method recovers primarily soluble proteins from the nucleus, not so much proteins bound in chromatin or integral membrane proteins of the nuclear envelope. The protein concentration of the nuclear extracts can be manipulated easily by varying the volume of nuclear extraction reagent (NER) used in the extraction without any significant loss in extraction efficiency. Specific extraction of nuclear proteins from cells is central to the success of many gene regulation studies. While a variety of methods exist to isolate nuclei and prepare nuclear protein extracts, most of these are lengthy processes requiring mechanical homogenization, freeze/thaw cycles, extensive centrifugation or dialysis steps that may compromise the integrity of many fragile nuclear proteins. The NE-PER Kit overcomes these problems, providing high-quality, concentrated nuclear protein extracts for use in EMSA and other analysis techniques.

Related Products
Subcellular Protein Fractionation Kit for Cultured Cells
Subcellular Protein Fractionation Kit for TissuesBenchtop Centrifuges
For Research Use Only. Not for use in diagnostic procedures.
Specifications
BufferLysis Buffer
Quantity15 mL
Reagent TypeCell Lysis Buffer, Detergent Solution, Subcellular Fractionation
Shipping ConditionAmbient
FormLiquid
Product LineNE-PER
Product TypeNuclear and Cytoplasmic Extraction Reagent
Unit SizeEach
Contents & Storage
Upon receipt store kit components at 4°C.

Frequently asked questions (FAQs)

How long does it take to complete the NE-PER Extraction reagents protocol?

Nuclear and cytoplasmic proteins can be isolated within 2 hours.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

After protein extraction using the NE-PER Extraction reagents, where is the genomic DNA located?

After extracting the nuclear proteins using the NER Reagent, genomic DNA will be located in the pellet.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

Are there any considerations when adding protease inhibitors to the CER I and NER Reagents?

EDTA-free Halt Protease and/or Phosphatase Inhibitor Cocktails (e.g., Cat. No. 78425) can be added to CER I and NER reagents. Most commercially available protease inhibitor cocktails are also compatible; however, avoid protease inhibitors that contain alcohols. Because the concentration of the CER I and NER Reagents are critical, do not dilute these reagents by more than 5% when adding protease inhibitors.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

Have the NE-PER Reagents been tested with plant tissue or yeast cells?

No. Also, nuclear protein was not successfully isolated from yeast cells that were pre-lysed with Y-PER Yeast Protein Extraction Reagent.

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

Is the final soluble nuclear fraction dialyzable when using the NE-PER Extraction reagents?

Yes. The nuclear fraction can be dialyzed in a Slide-A-Lyzer MINI Dialysis Unit (Cat. No. 69550) against a buffer, such as PBS, that is compatible with the specific downstream application. A buffer exchange can also be performed using the Thermo Scientific Protein Desalting Spin Columns (Cat. No. 89849) or Zeba Desalt Spin Columns (Cat. No. 89882).

Find additional tips, troubleshooting help, and resources within our Protein Purification and Isolation Support Center.

Citations & References (7)

Citations & References
Abstract
FOXO1 modulates osteoblast differentiation.
Authors:Siqueira MF,Flowers S,Bhattacharya R,Faibish D,Behl Y,Kotton DN,Gerstenfeld L,Moran E,Graves DT
Journal:Bone
PubMed ID:21281751
Forkhead box O1 (FOXO1) is upregulated during bone formation and in response to stimulation by bone morphogenetic proteins. Studies presented here examined the functional role of FOXO1 in a well defined culture system in which pre-osteoblastic cells undergo terminal differentiation in vitro. Mineralizing cultures of MC3T3-E1 cells were examined with ... More
Correlation between S100A11 and the TGF-β(1)/SMAD4 pathway and its effects on the proliferation and apoptosis of pancreatic cancer cell line PANC-1.
Authors:Ji YF,Li T,Jiang F,Ni WK,Guan CQ,Liu ZX,Lu CH,Ni RZ,Wu W,Xiao MB
Journal:Molecular and cellular biochemistry
PubMed ID:29922945
S100A11 as a S100 protein family member has been documented to play dual-direction regulation over cancer cell proliferation. We explored the role of S100A11 in the proliferation and apoptosis of pancreatic cancer cell line PANC-1 and the potential mechanisms involving the TGF-β(1)/SMAD4/p21 pathway. S100A11 and TGF-β(1) protein expressions in 30 ... More
An improved cell nuclear isolation method.
Authors:Li P,Zhang J,Liu X,Wu Z,Kang YJ,Zhang W
Journal:Biology methods & protocols
PubMed ID:39925781
Nuclear isolation is crucial for studying gene expression and regulatory mechanisms in eukaryotic cells. This study aimed to improve nuclear isolation and compare the yield, purity, and efficiency of several methods. Human umbilical vein endothelial cells were used to evaluate four different techniques: sucrose centrifugation, a simplified method, homogenization, and ... More
Conformation-Crooking CXCL4 to Unravel Autoimmune Heparin-Induced Thrombocytopenia.
Authors:Koenen RR
Journal:Thrombosis and haemostasis
PubMed ID:33385179
Human bile salt export pump promoter is transactivated by the farnesoid X receptor/bile acid receptor.
Authors:Ananthanarayanan M, Balasubramanian N, Makishima M, Mangelsdorf DJ, Suchy FJ
Journal:J Biol Chem
PubMed ID:11387316
'The bile salt excretory pump (BSEP, ABCb11) is critical for ATP-dependent transport of bile acids across the hepatocyte canalicular membrane and for generation of bile acid-dependent bile secretion. Recent studies have demonstrated that the expression of this transporter is sensitive to the flux of bile acids through the hepatocyte, possibly ... More