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Patch Clamp hERG Safety Testing Service

Patch Clamp hERG Safety Testing Services

hERG testing for drug candidates is a crucial element of drug development, as an estimated 25-40% of all lead compounds show some level of hERG related toxicity. As a result, regulatory agencies including FDA and EMEA require hERG/IKr pre-clinical safety data as part of any investigational new drug submission. The human cardiac delayed rectifier potassium current (IKr) is carried by a channel encoded by the human ether-a-go-go–related gene (hERG). Suppression of IKr by loss of function mutations in the hERG gene or by untoward drug block can prolong the QT interval and predispose patients to the potentially lethal arrhythmia Torsades de Pointes (TdP), is now well documented. GenScript helps our clients solve hERG safety issues at early discovery stages and during preclinical development.

In contrast to the cheaper automated hERG testing methods, manual patch clamp assays can achieve higher accuracy without any compromise, and therefore, provide the most reliable results.

GenScript’s premium technology and facilities enable the delivery of this valuable service to you at the most affordable price in market. All assays are performed using our robust hERG stable cell lines (HEK-293).
Patch Clamp hERG Safety Testing Service
  • hERG Safety Profiling Assay
  • Rapid Patch Screening Service
  • Sample Screening Results
Cell Line HEK-293
Technology Manual patch clamp
Compound 3 - 5 mg
Number of Compounds No limit
Concentrations 0.01 - 30 μM, depending on solubility
Number of Concentrations 3 - 4
Measurements 3
Positive Controls Terfenadine, astemizole, quinidine, and one positive control
Test Conditions Five to ten minutes of exposure at either room temperature or 37°C
Deliverables Report includes protocol summary, concentration-response curve, and IC50 value for each compound.
Turnaround time 1 - 2 weeks

Assays

a. Test 3 - 4 concentrations (n=3), plus positive control per study, such as terfenadine, astemizole, quinidine, etc.
b. Report includes protocol summary, plus concentration-response curve and IC50 value for each compound.

Sample Requirements

Required materials: 3 - 5 mg is sufficient for small molecules.

Study requirements: The client must provide GenScript with detailed study requirements.

Compound requirements: Customers must provide information on the physicochemical properties of the compounds to be tested, such as molecular weight, solubility, stability, and storage conditions.

Quotation and Ordering

hERG safety testing service To request a quotation, please download and complete the Quotation/Order Form, and send it to us by email or fax.quotation

hERG safety testing service To order, please download and complete the Quotation/Order Form and send it to us by email or fax with a formal PO (Purchase Order) or credit card information. You can also submit PO/credit card information by phone or via our Secure Online Messaging System.

hERG safety testing service If submitting samples, please mail them together with a hard copy of the completed Quotation/Order Form to: Gene Department, GenScript, 120 Centennial Ave., Piscataway, NJ 08854, US.

hERG safety testing service For questions, or to inquire about the status of your order contact us by email, phone, fax or via our Secure Online Messaging System.
Our customer service representatives are available 24 hours a day, Monday through Friday to assist you.

Email for Order & Quote: order@genscript.es
Phone: +1-732-885-9188 (USA)
Toll-Free: 800-098-920 (Spain)  +1-877-436-7274 (USA)

Fax: +1-732-210-0262   +1-732-885-5878