B-PER™ Complete Bacterial Protein Extraction Reagent
B-PER™ Complete Bacterial Protein Extraction Reagent
Thermo Scientific™

B-PER™ Complete Bacterial Protein Extraction Reagent

Thermo Scientific B-PER Complete Bacterial Protein Extraction Reagent is an easy-to-use cell lysis reagent is a nonionic detergent-based solutions thatRead more
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Catalog NumberQuantity
89822500 mL
89821250 mL
Catalog number 89822
Price (EUR)
930,00
Each
Add to cart
Quantity:
500 mL
Request bulk or custom format
Price (EUR)
930,00
Each
Add to cart
Thermo Scientific B-PER Complete Bacterial Protein Extraction Reagent is an easy-to-use cell lysis reagent is a nonionic detergent-based solutions that effectively disrupt cells and solubilize native or recombinant proteins without denaturation. All B-PER Reagents are compatible with downstream applications, such as affinity chromatography (e.g., immobilized metal affinity chromatography, glutathione chromatography), SDS-PAGE, and protein quantification (e.g., Pierce BCA Protein Assay, Pierce 660nm Protein Assay). Depending on the particular application, protease inhibitors, salts, reducing agents, denaturants, and chelating agents may be added to the reagent.

Features of the B-PER Bacterial Protein Extraction Reagent:

• Detergent in Tris buffer with Lysozyme and Universal Nuclease
• Improved cell lysis and DNA digestion, thereby releasing soluble proteins and reducing viscosity to increase yields
• Recovery of large molecular weight proteins (high MW proteins)
• Cost-effective equivalent to Merck Millipore Bugbuster™ Master Mix

B-PER Complete Bacterial Protein Extraction Reagent is an all-inclusive formulation that combines the lysis reagent with lysozyme and a universal nuclease to enable mild extraction from both gram-negative and gram-positive bacteria. Traditional Tris-buffered and phosphate-buffered formulations without enzymes are also offered. All B-PER Reagents are compatible with downstream applications, such as affinity chromatography (e.g., immobilized metal affinity chromatography, glutathione chromatography), SDS-PAGE, and protein quantification (e.g., Pierce BCA Protein Assay, Pierce 660nm Protein Assay). Depending on the particular application, protease inhibitors, salts, reducing agents, denaturants, and chelating agents may be added to the reagent.

All Thermo Scientific B-PER Protein Extraction Reagents are:
Ready to use—one-step cell lysis of gram-positive and gram-negative bacteria using a mild, nonionic detergent (proprietary) in Tris or phosphate buffer formulations
Fast and simple—just add B-PER Reagent to a bacterial pellet, incubate with mixing for 10 to 15 minutes and recover soluble proteins after pelleting the cell debris
Convenient B-PER Complete Reagent contains lysozyme and a universal nuclease in a single formulation with 4°C storage
Excellent yields—recover recombinant proteins from bacterial lysates or purify inclusion bodies to near-homogeneous levels
Flexible—B-PER Reagents are suitable for any scale of protein extraction and are available in phosphate and 1X and 2X Tris formulations, with and without enzymes
Compatible—completely compatible with addition of protease inhibitors, and the resulting protein extract can be used in protein assays, typical affinity purification methods (e.g., GST, 6xHis) and other applications

Convenient, Ready-to-use Formats
B-PER Bacterial Extraction Reagents are more effective than traditional sonication and typical homemade lysis buffers, many of which include detergents and components that interfere with downstream applications. B-PER Reagents are formulated in Tris or phosphate buffer at physiological pH. They extract native and soluble recombinant proteins and yield lysates that are directly compatible with most downstream workflows such as electrophoresis, affinity purification, immunoprecipitation, protein interaction analysis, crosslinking and protein labeling.

More Product Data
Improved, all-in-one B-PER Reagent for bacterial protein extraction

Related Products
B-PER™ Bacterial Protein Extraction Reagent
B-PER™ Reagent (in Phosphate Buffer)
B-PER™ II Bacterial Protein Extraction Reagent (2X)
For Research Use Only. Not for use in diagnostic procedures.
Specifications
FormulationProprietary detergent in 20mM Tris buffer, pH 7.5, containing lysozyme and universal nuclease
Quantity500 mL
Volume (Metric)500 mL
Product LineB-PER
Product TypeBacterial Protein Extraction Reagent
Unit SizeEach
Contents & Storage
Store at 4°C.

Frequently asked questions (FAQs)

What is the difference between B-PER and B-PER II Reagent?

B-PER II Reagent contains more detergent making it ideal for extracting proteins from small bacterial cultures with less than 20 mL in volume.

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

What is the composition of B-PER Reagent?

B-PER Reagent utilizes a proprietary, mild nonionic detergent in a 20 mM Tris HCl, pH 7.5 buffer. No enzymatic components are present in the B-PER solution itself (B-PER Complete Bacterial Protein Extraction Reagent, Cat. No. 89821, 89822 does contain enzymes). Depending on your particular protein, you may need to add components such as salt, lysozyme, protease inhibitors, reducing agents and chelating agents. Other ready-to-use formats include B-PER II Bacterial Protein Extraction Reagent (2X), B-PER Reagent (in Phosphate Buffer), and B-PER with Enzymes Bacterial Protein Extraction Kit.

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

What is the volume of B-PER Extraction Reagent to use per gram weight of wet cells?

For 1 gram of cells add 4 mL of B-PER Reagent.

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

Will my protein be in its native conformation after B-PER Reagent extraction?

While this is protein-dependent, many proteins have been successfully tested in downstream applications (reporter assays, immunoprecipitation and beta-Gal assays), including GST and 6xHis proteins. Otherwise, samples can be diluted or dialyzed to remove any interfering substances.

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

Why is my protein extract so viscous after B-PER Reagent extraction?

This is often an indication of the presence of large amounts of DNA in the extract. This viscosity will be greatly decreased upon addition of DNase I (Cat. No. 90083).

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

Citations & References (4)

Citations & References
Abstract
Controlling selectivity of modular microbial biosynthesis of butyryl-CoA-derived designer esters.
Authors:Lee JW,Trinh CT
Journal:Metabolic engineering
PubMed ID:34883244
Short-chain esters have broad utility as flavors, fragrances, solvents, and biofuels. Controlling selectivity of ester microbial biosynthesis has been an outstanding metabolic engineering problem. In this study, we enabled the de novo fermentative microbial biosynthesis of butyryl-CoA-derived designer esters (e.g., butyl acetate, ethyl butyrate, butyl butyrate) in Escherichia coli with ... More
A truncated isoform of Connexin43 caps actin to organize forward delivery of full-length Connexin43
Authors:Baum R, Nguyen VD, Maalouf M, Shimura D, Waghalter M, Srapyan S, Jin Q, Kuzmanovich L, Gaffney AT, Bell BR, Xiao S, Palatinus JA, Kléber AG, Grintsevich EE, Hong T, Shaw RM.
Journal:J Cell Biol
PubMed ID:39737876
While membrane proteins such as ion channels continuously turn over and require replacement, the mechanisms of specificity of efficient channel delivery to appropriate membrane subdomains remain poorly understood. GJA1-20k is a truncated Connexin43 (Cx43) isoform arising from translation initiating at an internal start codon within the same parent GJA1 mRNA ... More
Single mutation at a highly conserved region of chloramphenicol acetyltransferase enables isobutyl acetate production directly from cellulose by Clostridium thermocellum at elevated temperatures.
Authors:Seo H,Lee JW,Garcia S,Trinh CT
Journal:Biotechnology for biofuels
PubMed ID:31636704
BACKGROUND: Esters are versatile chemicals and potential drop-in biofuels. To develop a sustainable production platform, microbial ester biosynthesis using alcohol acetyltransferases (AATs) has been studied for decades. Volatility of esters endows high-temperature fermentation with advantageous downstream product separation. However, due to the limited thermostability of AATs known, the ester biosynthesis ... More
Efficient engineering of human and mouse primary cells using peptide-assisted genome editing.
Authors:Zhang Z,Baxter AE,Ren D,Qin K,Chen Z,Collins SM,Huang H,Komar CA,Bailer PF,Parker JB,Blobel GA,Kohli RM,Wherry EJ,Berger SL,Shi J
Journal:Nature biotechnology
PubMed ID:37095348
Simple, efficient and well-tolerated delivery of CRISPR genome editing systems into primary cells remains a major challenge. Here we describe an engineered Peptide-Assisted Genome Editing (PAGE) CRISPR-Cas system for rapid and robust editing of primary cells with minimal toxicity. The PAGE system requires only a 30-min incubation with a cell-penetrating ... More