Cartridge Sample Clauses

Cartridge. A customer replaceable module that holds toner or ink and that must be inserted into or connected to an imaging equipment Product for the imaging equipment Product during print. Ink and toner bottles or similar units designed to refill ink or toner tanks are not “Cartridges” for the purposes of this Voluntary Agreement.
Sample 1Sample 2
AutoNDA by SimpleDocs
Cartridge. 4-1 Unit Price US$fully burdened cost plus 15%
Sample 1
Cartridge. Each cartridge consists of a printed circuit board (PCB) with an array of gold electrodes on one face of the PCB. Each electrode is approximately 0.5 mm in diameter. Each electrode is connected to a contact paid on one edge of the PCB via a thin interconnect strip of metal. The exposed area of each electrode is defined by one or more layers of solder mask (a photosensitive insulating layer). Each electrode is covered by the solder mask, except for a circle in its center of approximately 0.25 mm diameter. The solder mask completely covers the entire surface of the PCB except for the electrodes and the connector pads on one edge of the PCB. The electrodes of each PCB “chip” are modified with a self-assembled-monolayer (XXX) containing insulating molecules and DNA oligonucleotides (15-30 nucleotides in length). The insulating molecules are thio-alkyl or disulfide-alkyl compounds which have appended triethylene-glycol groups. The DNA oligonucleotides are modified (usually on the 3’ terminal nucleotide) with an thio-alkyl group. The electrodes are modified by applying a small droplet of the two components in an aqueous solution to each electrode using a non-contact automated spotter. Each electrode can be modified with a different oligonucleotide sequence or multiple electrodes can be modified with the same oligonucleotide. The cartridge is formed by attaching the modified PCB to a plastic housing. The plastic housing and a gasket define a fluid chamber over the electrode array. The plastic housing and gasket also form an inlet port to the cartridge designed to accept a standard disposable pipet tip for filling. The cartridges in an Assay Kit are enclosed in a metalized plastic pouch which is filled with nitrogen gas.
Sample 1
Cartridge. Each cartridge consists of a printed circuit board (PCB) with an array of 36 gold electrodes on one face of the PCB. The gold electrodes are formed by electroplating first tin and then gold over copper. Electrodes, interconnects and edge contacts are all coated with electroplated gold. The exposed area of each electrode is defined by two layers of solder mask. Each electrode is covered by a first layer of solder mask, except for a circle in its center of 0.25 mm diameter. The second (top) solder mask layer has a larger circular hole (approximately 1 mm in diameter) around each DNA electrode. Each PCB also has a single reference electrode which is gold, but coated with a Ag/AgCl paste. Each PCB also has a single auxiliary electrode which is a gold electrode of approximately 1 mm diameter. Each electrode is spotted with different capture probe, usually 20-25 nucleotides in length. Typically, two electrodes are coated with each capture probe to provide duplicate analysis for increased reliability of the assay. Two positive control electrodes are spotted with a capture probe which will hybridize with a synthetic DNA oligonuclotide which is included in the assay buffer. The assay buffer also contains a signal probe complementary to the synthetic oligonuclotide. Two negative control electrodes are also included and spotted with capture probes that have no significant complementarity to any signal probe or target polynucleotide. The cartridge is formed by attaching the modified PCB to a plastic housing. The plastic housing and a double sided adhesive gasket define a fluid chamber over the electrode array.
Sample 1
Cartridge. Each cartridge will consist of a printed circuit board (PCB) with an array of 75-100 gold electrodes on the PCB. A higher density edge connector configuration will be employed to allow the higher number of electrodes. The cartridges are designed to allow mixing of the fluid contained in the cartridge to facilitate hybridization kinetics. SCHEDULE 7 Royalty Reports Royalty reports are required from the Licensee and each Affiliate for each Calendar Quarter during the Term. Each report is to contain information that enables OGT to check the volume and the value of each form of Net Sales interaction as expressly allowed by the Agreement. Each report should contain the following sections
Sample 1

Related to Cartridge

  • API If the Software offers integration capabilities via an API, your use of the API may be subject to additional costs or Sage specific policies and terms and conditions (which shall prevail in relation to your use of the API). You may not access or use the API in any way that could cause damage to us or the Software, or in contravention of any applicable laws. We reserve the right in our sole discretion, to: (i) update any API from time to time; (ii) place limitations around your use of any API; and (iii) deny you access to any API in the event of misuse by you or to otherwise protect our legitimate interests.

  • Packaging Materials and Containers for Retail Sale Packaging materials and containers in which a good is packaged for retail sale shall, if classified with the good, be disregarded in determining whether all the non-originating materials used in the production of the good undergo the applicable change in tariff classification set out in Annex 4, and, if the good is subject to a regional value-content requirement, the value of such packaging materials and containers shall be taken into account as originating or non-originating materials, as the case may be, in calculating the regional value content of the good.

  • FABRICATION Making up data or results and recording or reporting them.

  • SAMPLE (i) Unless agreed otherwise, wheeled or track lay- ing equipment shall not be operated in areas identified as needing special measures except on roads, landings, tractor roads, or skid trails approved under B5.1 or B6.422. Purchaser may be required to backblade skid trails and other ground disturbed by Purchaser’s Opera- tions within such areas in lieu of cross ditching required under B6.6. Additional special protection measures needed to protect such known areas are identified in C6.24.

  • Consumables During the design phase, Purchaser may participate in the selection of suppliers of consumables of the Supplier. In such case, the choice regarding the final selection of the said suppliers shall be mutually agreed between the Parties. Two suppliers shall be identified and selected for each type of consumables.

  • Product ACCEPTANCE Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User(s) shall have thirty (30) days from the date of delivery to accept hardware products and sixty (60) days from the date of delivery to accept all other Product. Where the Contractor is responsible for installation, acceptance shall be from completion of installation. Failure to provide notice of acceptance or rejection or a deficiency statement to the Contractor by the end of the period provided for under this clause constitutes acceptance by the Authorized User(s) as of the expiration of that period. The License Term shall be extended by the time periods allowed for trial use, testing and acceptance unless the Commissioner or Authorized User agrees to accept the Product at completion of trial use. Unless otherwise provided by mutual agreement of the Authorized User and the Contractor, Authorized User shall have the option to run testing on the Product prior to acceptance, such tests and data sets to be specified by User. Where using its own data or tests, Authorized User must have the tests or representative set of data available upon delivery. This demonstration will take the form of a documented installation test, capable of observation by the Authorized User, and shall be made part of the Contractor’s standard documentation. The test data shall remain accessible to the Authorized User after completion of the test. In the event that the documented installation test cannot be completed successfully within the specified acceptance period, and the Contractor or Product is responsible for the delay, Authorized User shall have the option to cancel the order in whole or in part, or to extend the testing period for an additional thirty (30) day increment. Authorized User shall notify Contractor of acceptance upon successful completion of the documented installation test. Such cancellation shall not give rise to any cause of action against the Authorized User for damages, loss of profits, expenses, or other remuneration of any kind. If the Authorized User elects to provide a deficiency statement specifying how the Product fails to meet the specifications within the testing period, Contractor shall have thirty (30) days to correct the deficiency, and the Authorized User shall have an additional sixty (60) days to evaluate the Product as provided herein. If the Product does not meet the specifications at the end of the extended testing period, Authorized User, upon prior written notice to Contractor, may then reject the Product and return all defective Product to Contractor, and Contractor shall refund any monies paid by the Authorized User to Contractor therefor. Costs and liabilities associated with a failure of the Product to perform in accordance with the functionality tests or product specifications during the acceptance period shall be borne fully by Contractor to the extent that said costs or liabilities shall not have been caused by negligent or willful acts or omissions of the Authorized User’s agents or employees. Said costs shall be limited to the amounts set forth in the Limitation of Liability Clause for any liability for costs incurred at the direction or recommendation of Contractor.

  • Manufacturing (a) The Supplier shall without limitation be responsible, at no additional cost to the Purchaser, for: sourcing and procuring all raw materials for the Products; obtaining all necessary approvals, permits and licenses for the manufacturing of the Products; providing sufficient qualified staff and workers to perform the obligations under this Purchase Agreement; implementing and maintaining effective inventory and production control procedures with respect to the Products; and handling other matters as reasonably requested by the Purchaser from time to time.

  • Catalog Information about Community Regional Medical Center – Diagnostic Medical Sonography Program (CRMC-DMSP) is published in a school catalog that contains a description of certain policies, procedures, and other information about the school. CRMC-DMSP reserves the right to change any provision of the catalog at any time. Notice of changes will be communicated in a revised catalog, an addendum or supplement to the catalog, or other written format. Students are expected to read and be familiar with the information contained in the school catalog, in any revisions, supplements and addenda to the catalog, and with all school policies. By enrolling in CRMC-DMSP, the Student agrees to abide by the terms stated in the catalog and all school policies.

  • Cookies We and Our partners may use various technologies to collect and store information when You use this Website, and this may include using cookies and similar tracking technologies, such as pixels and web beacons. These web beacons track certain behavior such as whether the email sent through the Website was delivered and opened and whether links within the email were clicked. They also allow Us to collect information such as the recipient’s: • IP address, browser, email client type and other similar details; • Tracking Website usage and traffic; • Reports are available to Us when We send email to You, so We may collect and review that information. These cookies do not read Your hard drive but may be stored on Your hard drive to enable Our Website to recognise You when You return to the same. Mailing Lists If at any time You are on a mailing list of Ours then You may request to be removed from the same and We will comply with Your request if there is no unsubscribe button provided then please contact Us with Your request using the “Contact Us” section of this Website.

  • RE-WEIGHING PRODUCT Deliveries are subject to re- weighing at the point of destination by the Authorized User. If shrinkage occurs which exceeds that normally allowable in the trade, the Authorized User shall have the option to require delivery of the difference in quantity or to reduce the payment accordingly. Such option shall be exercised in writing by the Authorized User.

Time is Money Join Law Insider Premium to draft better contracts faster.