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Liofilchem® ESBL Disc Kit (acc. to EUCAST) for 50 tests

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SKU: 99004
Brand: Liofilchem
UoM: Kit
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Store Availability & Pickup
LabMart Limited - Tamale
NS-246, Via, 4388 Tamale-Kumbungu Rd, Tamale, Northern Region, Ghana
Not available
LabMart Limited
10 Rcecourse street, Accra, Greater Accra Region, Ghana
Not available
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MOQ : 1.0 Kit
Estimated delivery Estimated delivery: 4-8 weeks
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The Liofilchem® ESBL Disc Kit is designed for the phenotypic confirmation of Extended-Spectrum β-Lactamase (ESBL)-producing Enterobacteriaceae, in accordance with EUCAST standards. Below are the details of the kit's components and references.

Kit Components

  1. Disc Types:
    • Cefotaxime (CTX) 30 µg: Indicator cephalosporin.
    • Cefotaxime + Clavulanic Acid (CTL) 40 µg (30 + 10 µg): For detecting synergy with clavulanic acid.
    • Ceftazidime (CAZ) 30 µg: Indicator cephalosporin.
    • Ceftazidime + Clavulanic Acid (CAL) 40 µg (30 + 10 µg): Detecting synergy.
    • Cefepime (FEP) 30 µg: For organisms with suspected AmpC activity.
    • Cefepime + Clavulanic Acid (FEL) 40 µg (30 + 10 µg): Detects synergy in AmpC producers.
  2. Packaging:
    • Cartridges with 6 x 50 discs each, packaged in blisters with a desiccant to ensure stability.
  3. Storage Instructions:
    • Store at -20°C to +8°C.
    • Open cartridges at room temperature to avoid condensation.
    • Unused discs should be returned to 2-8°C and used within 7 days.

Testing Principle

  • Combination Disc Test (CDT):
    • Tests the inhibitory synergy of clavulanic acid with cefotaxime, ceftazidime, or cefepime.
    • A positive result is indicated by an ≥ 5 mm increase in inhibition zone diameter for the cephalosporin when combined with clavulanic acid.

Quality Control

  • Positive Controls:
    • Klebsiella pneumoniae ATCC® 700603 (SHV-18 ESBL producer).
    • Escherichia coli NCTC 13353 (CTX-M-15 ESBL producer).
  • Negative Control:
    • Escherichia coli ATCC® 25922.

References

  1. EUCAST Technical Guidance (2019): "New disk potencies for combination disks containing cefotaxime and ceftazidime with and without clavulanic acid."
  2. EUCAST Guidelines (Version 2.0, 2017): "Detection of resistance mechanisms and specific resistances of clinical and/or epidemiological importance."

Application: Clinical microbiology
Storage Temperature: -20°C
Product Type: Antibiotic Disc
Product Brand: Liofilchem
Product Grade: Microbiology grade

The Liofilchem® ESBL Disc Kit is designed for the phenotypic confirmation of Extended-Spectrum β-Lactamase (ESBL)-producing Enterobacteriaceae, in accordance with EUCAST standards. Below are the details of the kit's components and references.

Kit Components

  1. Disc Types:
    • Cefotaxime (CTX) 30 µg: Indicator cephalosporin.
    • Cefotaxime + Clavulanic Acid (CTL) 40 µg (30 + 10 µg): For detecting synergy with clavulanic acid.
    • Ceftazidime (CAZ) 30 µg: Indicator cephalosporin.
    • Ceftazidime + Clavulanic Acid (CAL) 40 µg (30 + 10 µg): Detecting synergy.
    • Cefepime (FEP) 30 µg: For organisms with suspected AmpC activity.
    • Cefepime + Clavulanic Acid (FEL) 40 µg (30 + 10 µg): Detects synergy in AmpC producers.
  2. Packaging:
    • Cartridges with 6 x 50 discs each, packaged in blisters with a desiccant to ensure stability.
  3. Storage Instructions:
    • Store at -20°C to +8°C.
    • Open cartridges at room temperature to avoid condensation.
    • Unused discs should be returned to 2-8°C and used within 7 days.

Testing Principle

  • Combination Disc Test (CDT):
    • Tests the inhibitory synergy of clavulanic acid with cefotaxime, ceftazidime, or cefepime.
    • A positive result is indicated by an ≥ 5 mm increase in inhibition zone diameter for the cephalosporin when combined with clavulanic acid.

Quality Control

  • Positive Controls:
    • Klebsiella pneumoniae ATCC® 700603 (SHV-18 ESBL producer).
    • Escherichia coli NCTC 13353 (CTX-M-15 ESBL producer).
  • Negative Control:
    • Escherichia coli ATCC® 25922.

References

  1. EUCAST Technical Guidance (2019): "New disk potencies for combination disks containing cefotaxime and ceftazidime with and without clavulanic acid."
  2. EUCAST Guidelines (Version 2.0, 2017): "Detection of resistance mechanisms and specific resistances of clinical and/or epidemiological importance."

No resources are currently available for this product.

This will display Shipping & Return.

The Liofilchem® ESBL Disc Kit is designed for the phenotypic confirmation of Extended-Spectrum β-Lactamase (ESBL)-producing Enterobacteriaceae, in accordance with EUCAST standards. Below are the details of the kit's components and references.

Kit Components

  1. Disc Types:
    • Cefotaxime (CTX) 30 µg: Indicator cephalosporin.
    • Cefotaxime + Clavulanic Acid (CTL) 40 µg (30 + 10 µg): For detecting synergy with clavulanic acid.
    • Ceftazidime (CAZ) 30 µg: Indicator cephalosporin.
    • Ceftazidime + Clavulanic Acid (CAL) 40 µg (30 + 10 µg): Detecting synergy.
    • Cefepime (FEP) 30 µg: For organisms with suspected AmpC activity.
    • Cefepime + Clavulanic Acid (FEL) 40 µg (30 + 10 µg): Detects synergy in AmpC producers.
  2. Packaging:
    • Cartridges with 6 x 50 discs each, packaged in blisters with a desiccant to ensure stability.
  3. Storage Instructions:
    • Store at -20°C to +8°C.
    • Open cartridges at room temperature to avoid condensation.
    • Unused discs should be returned to 2-8°C and used within 7 days.

Testing Principle

  • Combination Disc Test (CDT):
    • Tests the inhibitory synergy of clavulanic acid with cefotaxime, ceftazidime, or cefepime.
    • A positive result is indicated by an ≥ 5 mm increase in inhibition zone diameter for the cephalosporin when combined with clavulanic acid.

Quality Control

  • Positive Controls:
    • Klebsiella pneumoniae ATCC® 700603 (SHV-18 ESBL producer).
    • Escherichia coli NCTC 13353 (CTX-M-15 ESBL producer).
  • Negative Control:
    • Escherichia coli ATCC® 25922.

References

  1. EUCAST Technical Guidance (2019): "New disk potencies for combination disks containing cefotaxime and ceftazidime with and without clavulanic acid."
  2. EUCAST Guidelines (Version 2.0, 2017): "Detection of resistance mechanisms and specific resistances of clinical and/or epidemiological importance."

No resources are currently available for this product.

This will display Shipping & Return.