Zeba™ Spin Desalting Columns, Plates, and Cartridges, 7K MWCO, 0.5–100 mL
Zeba™ Spin Desalting Columns, Plates, and Cartridges, 7K MWCO, 0.5–100 mL
Thermo Scientific™

Zeba™ Spin Desalting Columns, Plates, and Cartridges, 7K MWCO, 0.5–100 mL

Perform high-throughput protein recovery (7K MWCO) and sample desalting for mass spectrometry, HPLC, capillary electrophoresis, metabolite screening, and assay development with ready-to-use Thermo Scientific Pierce Zeba desalting chromatography columns, plates, and cartridges.
Have Questions?
Change viewbuttonViewtableView
Catalog NumberQuantityFormatVolume (Metric)
898935 ColumnsSpin Column10 mL
8987725 ColumnsSpin Column75 μL
8987850 ColumnsSpin Column75 μL
A400024695 ColumnsSpin Column20 mL
A4000247510 ColumnsSpin Column20 mL
8989025 ColumnsSpin Column2 mL
898915 ColumnsSpin Column5 mL
8989225 ColumnsSpin Column5 mL
8989425 ColumnsSpin Column10 mL
898895 ColumnsSpin Column2 mL
8988225 ColumnsSpin Column0.5 mL
8988350 ColumnsSpin Column0.5 mL
899345 columns x 1 mLChromatography Cartridge1 mL
899351 column x 5 mLChromatography Cartridge5 mL
898072 Plates96-well Filter Plate96-well
898084 Plates96-well Filter Plate96-well
Catalog number 89893
Price (KRW)
145,000
Precio exclusivo en nuestra web
Ends: 30-Jun-2025
165,000
Save 20,000 (12%)
Each
-
Add to cart
Quantity:
5 Columns
Format:
Spin Column
Volume (Metric):
10 mL
Request bulk or custom format
Price (KRW)
145,000
Precio exclusivo en nuestra web
Ends: 30-Jun-2025
165,000
Save 20,000 (12%)
Each
Add to cart
Ask our AI about this Product
Perform high-throughput protein recovery and sample desalting for mass spectrometry, HPLC, capillary electrophoresis, metabolite screening, and assay development with ready-to-use Pierce Zeba desalting chromatography columns, plates, and cartridges. Rapidly desalt protein and biological samples for manual or automated liquid chromatography (LC) with ≥95% retention of salts and other small molecular contaminants (<1,000 Da).

These Zeba spin desalting products contain a proprietary high-performance size-exclusion chromatography resin that enables excellent protein desalting and recovery of 7K molecular weight cutoff (MWCO) molecules using a centrifuge format. This resin is ideal for removing low molecular weight compounds including salts, fluorescent dyes, biotin, and other small labelling reagents.

Benefits of Zeba desalting columns, plates, and cartridges include:

  • High recovery—low-binding resin maximizes protein recovery,
  • Fast—no fraction screening or waiting for protein to emerge by gravity flow
  • Economical—great performance at lower cost than other commercially available cartridges
  • Easy-to-use—no cumbersome column preparation or equilibration
  • Flexible—available in spin columns, filter spin plates, and cartridges for a range of needs 

Zeba Spin Desalting Columns 

Convenient, ready-to-use polypropylene columns are the ideal solution for quick and straightforward desalting and buffer exchange of protein samples in a centrifuge format. The pre-dispensed spin columns are offered in various resin fills (75 μL, 0.5 mL, 2 mL, 5 mL, 10 mL, 20 mL). These options make it simple to handle sample volumes between 2 μL and 10 mL.

Zeba Desalting Plates

Provide trouble-free high-throughput desalting and buffer exchange for sample volumes ranging from 20 to 100 μL. Pre-dispensed 96-well filter plates require no resin dispensing or hydration and provide the same high protein recovery as spin columns with at least 95% removal of salts and other small molecules. One plate can process 96 small sample volumes (20 to 100 μL) in five minutes. Compatible with centrifugation for manual or automated purification.

Zeba Desalting Chromatography Cartridges

Compatible with automated liquid chromatography systems and with syringe processing, Zeba desalting cartridges provide fast, easy, and reproducible chromatographic separations and can be regenerated for multiple uses.

For Research Use Only. Not for use in diagnostic procedures.
Specifications
Product TypeSpin Desalting Column
Purification TargetBuffer Exchange, Protein
Quantity5 Columns
Volume (Metric)10 mL
Column TypeSize-exclusion, Proprietary Resin
FormatSpin Column
MWCO7.0 kDa
Product LineZeba™
Sample Volume (Metric)700 to 4000 μL
Unit SizeEach
Contents & Storage
Upon receipt store at 4°C.
Have questions about this product? Ask our AI assisted search.
Can I use Nunc White 384-Well Microplates for fluorescent assays?
Do you offer Nunc Microplate Lids for the Nunc Black or White 384-Well Microplates?
Why do you offer Nunc 384-Well Black or White Microplates when the cells cannot be observed using an inverted light microscope?
This is an AI-powered search and may not always get things right. You can help us make it better with a thumbs up or down on individual answers or by selecting the “Give feedback" button. Your search history and customer login information may be retained by Thermo Fisher and processed in accordance with our Privacy Notice.

Figures

Videos

Zeba Protein Desalting Spin Columns and 96-Well Spin Plates

Video Player is loading.
Current Time 0:00
Duration 0:00
Loaded: 0%
Stream Type LIVE
Remaining Time 0:00
 
1x
    • Chapters
    • descriptions off, selected
    • captions off, selected

      Customers who viewed this item also viewed



      Documents & Downloads

      Certificates

      Lot #Certificate TypeDateCatalog Number(s)
      3212089Certificate of AnalysisJun 26, 202589882
      3213798ACertificate of AnalysisJun 25, 202589890
      3213798Certificate of AnalysisJun 25, 202589890
      3215396Certificate of AnalysisJun 24, 202589877
      3215397Certificate of AnalysisJun 24, 202589877
      5 results displayed, search above for a specific certificate

      Safety Data Sheets

      Frequently asked questions (FAQs)

      You may remove excess solvent and smaller moieties by centrifugation through a microconcentrator. This will concentrate your protein sample.

      (1) Choose microconcentrator tube (available from a variety of commercial suppliers) with a protein cutoff smaller than the molecular weight of the protein in the sample. Check our Pierce Protein Concentrators PES.

      (2) Add 1 µL of 20% w/v SDS to a dry microconcentrator tube (if sample does not already contain SDS).

      (3) Slowly add sample (a few microliters at a time) to membrane until membrane is completely wet. Centrifuge to near (but not complete) dryness.

      (4) If intention is to desalt sample or buffer exchange: Add ~50 µL water to microconcentrator and spin until nearly dry. Repeat buffer exchange. Sample will remain on membrane. Check our Zeba desalting proteins.

      (5) Using a new collection tube, invert membrane and spin at low speed (1000 x g) to elute protein from membrane. Add 2X SDS-Sample Buffer containing 10 mM DTT to membrane: vortex, invert and spin. Final volume should be ~20 µL.

      Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.

      We recommend using Zeba Spin Desalting Columns, Plates, and Cartridges (Cat. No. 89882, 89883) to remove sodium azide from the Alix Monoclonal Antibody (3A9) storage solution.

      Zeba Spin Desalting columns are covered under our general 1-year warranty and are guaranteed to be fully functional for 12 months from the date of shipment, if stored as recommended. Please see section 8.1 of our Terms & Conditions of Sale (https://www.thermofisher.com/content/dam/LifeTech/Documents/PDFs/Terms-and-Conditions-of-Sale.pdf).

      Find additional tips, troubleshooting help, and resources within our Protein Dialysis, Desalting, and Concentration Support Center.

      Glycerol and sugars add viscosity to a sample, while detergents create micelles, making the removal of each difficult. Although dialysis is a better choice for removing these components, Zeba Columns can be used by modifying the desalting protocol. Modifications include diluting the samples, processing smaller samples, and adding the sample slowly to the column allowing it to enter the gel and equilibrate into the pores before centrifugation.

      Find additional tips, troubleshooting help, and resources within our Protein Dialysis, Desalting, and Concentration Support Center.

      You can either reduce the volume of sample processed in each column (the product manual indicates the volume range recommended for each column size) or run the flow-through from one column over a fresh column.

      Citations & References (15)

      Citations & References
      Abstract
      Cardioprotective O-GlcNAc signaling is elevated in murine female hearts via enhanced O-GlcNAc transferase activity.
      Authors:Narayanan B,Sinha P,Henry R,Reeves RA,Paolocci N,Kohr MJ,Zachara NE
      Journal:The Journal of biological chemistry
      PubMed ID:37949223
      The post-translational modification of intracellular proteins by O-linked β-GlcNAc (O-GlcNAc) has emerged as a critical regulator of cardiac function. Enhanced O-GlcNAcylation activates cytoprotective pathways in cardiac models of ischemia-reperfusion (I/R) injury; however, the mechanisms underpinning O-GlcNAc cycling in response to I/R injury have not been comprehensively assessed. The cycling of ... More
      Ethinylestradiol in combined hormonal contraceptive has a broader effect on serum proteome compared with estradiol valerate: a randomized controlled trial.
      Authors:Kangasniemi MH,Arffman RK,Joenväärä S,Haverinen A,Luiro K,Tohmola T,Renkonen R,Heikinheimo O,Tapanainen JS,Piltonen TT
      Journal:Human reproduction (Oxford, England)
      PubMed ID:36416543
      STUDY QUESTION: Does an estradiol-based combined oral contraceptive (COC) have a milder effect on the serum proteome than an ethinylestradiol (EE)-based COC or dienogest (DNG) only? SUMMARY ANSWER: The changes in serum proteome were multifold after the use of a synthetic EE-based COC compared to natural estrogen COC or progestin-only ... More
      Antibody-dependent enhancement of toxicity of myotoxin II from Bothrops asper.
      Authors:Sørensen CV,Fernández J,Adams AC,Wildenauer HHK,Schoffelen S,Ledsgaard L,Pucca MB,Fiebig M,Cerni FA,Tulika T,Voldborg BG,Karatt-Vellatt A,Morth JP,Ljungars A,Grav LM,Lomonte B,Laustsen AH
      Journal:Nature communications
      PubMed ID:38228619
      Improved therapies are needed against snakebite envenoming, which kills and permanently disables thousands of people each year. Recently developed neutralizing monoclonal antibodies against several snake toxins have shown promise in preclinical rodent models. Here, we use phage display technology to discover a human monoclonal antibody and show that this antibody causes antibody-dependent ... More
      Ubiquitin-driven protein condensation stabilizes clathrin-mediated endocytosis.
      Authors:Yuan F,Gollapudi S,Day KJ,Ashby G,Sangani A,Malady BT,Wang L,Lafer EM,Huibregtse JM,Stachowiak JC
      Journal:PNAS nexus
      PubMed ID:39253396
      Clathrin-mediated endocytosis is an essential cellular pathway that enables signaling and recycling of transmembrane proteins and lipids. During endocytosis, dozens of cytosolic proteins come together at the plasma membrane, assembling into a highly interconnected network that drives endocytic vesicle biogenesis. Recently, multiple groups have reported that early endocytic proteins form ... More
      Microscale Thermophoresis (MST) as a Tool to Study Binding Interactions of Oxygen-Sensitive Biohybrids.
      Authors:Jagilinki BP,Willis MA,Mus F,Sharma R,Pellows LM,Mulder DW,Yang ZY,Seefeldt LC,King PW,Dukovic G,Peters JW
      Journal:Bio-protocol
      PubMed ID:39131194
      Microscale thermophoresis (MST) is a technique used to measure the strength of molecular interactions. MST is a thermophoretic-based technique that monitors the change in fluorescence associated with the movement of fluorescent-labeled molecules in response to a temperature gradient triggered by an IR LASER. MST has advantages over other approaches for ... More
      15 total citations

      Other products to consider



      Share catalog number, name or link

      1x1 image pixel for data collection