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Empore SPE Disks

matrix active group C18, diam. 47 mm, pk of 20

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NACRES:
NB.21

description

C18

product line

Empore

packaging

pk of 20

manufacturer/tradename

CDS Analytical 98-0604-0217-3

technique(s)

solid phase extraction (SPE): suitable

diam.

47 mm

membrane thickness

0.5 mm

matrix active group

C18

particle size

12 μm

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General description

Empore membrane SPE technology comprises of SPE particles tightly enmeshed within a network of inert PTFE fibrils (90% SPE particles : 10% PTFE, by weight). The SPE-membrane fabrication process results in a highly dense and uniform extraction medium that offers distinct advantages over traditional sorbent/packed-bed SPE products. Empore SPE technology provides a denser, more uniform extraction bed than traditional packed bed products allowing for smaller bed weights, shorter analyte to pore diffusion paths, and more efficient extractions.

The Empore line of SPE disks comprises of the most complete line of SPE disks for extracting large volumes of aqueous samples. The product line ranges from time-tested C18 to unique phase chemistries such as carbon and the highly polar Oil & Grease disk. The disks are ideal for environmental analysis where 1 L sample volumes are not uncommon and provide an efficient alternative to LLE.

Save Time & Money:
  • Reduced SPE Bed Mass = Reduced SPE Solvent & Elution Volumes
  • Minimize SPE eluate evaporation time
  • Potentially allows for direct injection of the SPE eluate
  • Dense & Uniform Extraction Medium = No SPE Channeling and Voiding
  • Efficient mass-transfer kinetics allow for faster flow rates
  • Eliminate SPE fines improving column and instrument life

Application

Ideal for the extraction of semi- and non-volatile compounds from water and soil. Applicable for use with:
  • EPA Method 506 - Phthlate & Adipate Esters
  • EPA Method 508.1 - Chlorinated Pesticides, Herbicides and Organohalides
  • EPA Method 525.2 - Semi-Volatile Organic Compounds
  • EPA Method 532 - Phenylurea Pesticides
  • EPA Method 550.1 - PAHs
  • EPA Method 553 - Benzidines and Nitrogen-Containing Pesticides
  • EPA Method 554 - Carbonyl Compounds
  • EPA Method 555 - Chlorinated Acids
  • 608ATP3M0222 - Organochlorine Pesticides and PCBs
  • 1613B - Dioxins and Furans
  • 3535 - Organichlorine Pesticides & Phthalate Esters
  • 8330A - Nitroaromatics & Nitroamines
  • 8095 - Explosives
  • 8323 - Organotins
  • 8321b - Solvent extractable non-volatile compounds
  • Dioxin DLM01.1 - Octo-chlorinated Dibenzo-p-dioxins (CDDs) and Dibenzofurans (CDFs)

Legal Information

Empore is a trademark of CDS Analytical

Disclaimer

CDS Analytical LLC recently acquired the rights to Empore products from 3M Purification Inc. For an interim phase, you may receive products packaged with either manfacturer′s branding.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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Fabrizia Brisdelli et al.
International journal of molecular sciences, 21(1) (2019-12-22)
Among natural products under investigation for their additive potential in cancer prevention and treatment, the flavonoid quercetin has received attention for its effects on the cell cycle arrest and apoptosis. In the past, we addressed this issue in K562 cells
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Cell reports, 30(1), 25-36 (2020-01-09)
Known as a histone H3K9 methyltransferase, SETDB1 is essential for embryonic development and pluripotent inner cell mass (ICM) establishment. However, its function in pluripotency regulation remains elusive. In this study, we find that under the "ground state" of pluripotency with
Heeseon An et al.
Molecular cell, 74(5), 891-908 (2019-04-23)
Cells respond to nutrient stress by trafficking cytosolic contents to lysosomes for degradation via macroautophagy. The endoplasmic reticulum (ER) serves as an initiation site for autophagosomes and is also remodeled in response to nutrient stress through ER-phagy, a form of
Alban Ordureau et al.
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Flux through kinase and ubiquitin-driven signaling systems depends on the modification kinetics, stoichiometry, primary site specificity, and target abundance within the pathway, yet we rarely understand these parameters and their spatial organization within cells. Here we develop temporal digital snapshots
Michal Harel et al.
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Immunotherapy has revolutionized cancer treatment, yet most patients do not respond. Here, we investigated mechanisms of response by profiling the proteome of clinical samples from advanced stage melanoma patients undergoing either tumor infiltrating lymphocyte (TIL)-based or anti- programmed death 1

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