Procedures for cleaning flow cells for Illumina sequencers

iSeq 100

• No cleaning required.

• Only touch the plastic when handling the flow cell.

• Avoid touching the electrical interface, CMOS sensor, glass, and gaskets on either side of the glass.

• Reference: iSeq 100 Sequencing System Product Documentation.

MiniSeq

• Put on a new pair of powder-free gloves.

• Remove the flow cell from the container.

• Clean the glass surface of the flow cell with a lint-free alcohol wipe.

• Dry with a lint-free lens cleaning tissue. Use care around the black flow cell gasket.

• Inspect the flow cell port for obstructions. Make sure that the gasket is well-seated.

• Reference: MiniSeq System Guide.

MiSeq

• Put on a new pair of powder-free gloves.

• Remove the flow cell from the container.

• Lightly rinse the flow cell with laboratory grade water until both the glass and the plastic cartridge are thoroughly rinsed of excess salts.

• Using care around the black flow cell port gasket, thoroughly dry the flow cell glass and plastic with a lint-free lens cleaning tissue. Gently pat dry in the area of the gasket and adjacent glass.

• Clean the flow cell glass with an alcohol wipe. Make sure that the glass is free of streaks, fingerprints, and lint or tissue fibres.

• DO NOT USE THE ALCOHOL WIPE ON THE FLOW CELL PORT GASKET.

• Dry excess alcohol with a lint-free lens cleaning tissue.

• Inspect the flow cell port for obstructions. Make sure that the gasket is well-seated. If the gasket appears to be dislodged, gently press it back until it sits securely around the flow cell ports.

• Reference: MiSeq System Guide for Windows 10 and MiSeq System Guide for Windows 7.

NextSeq 500/550

• Remove the flow cell from the foil packaging.

• Open the clear plastic clamshell package and remove the flow cell.

• Clean the glass surface of the flow cell with a lint-free alcohol wipe. Dry the glass with a low-lint lab tissue.

• Reference: NextSeq 500 and NextSeq 550 Sequencing System Guide

NextSeq 1000/2000

• The flow cell MUST NOT be cleaned.

• Flow cells can look streaky; they are fine to use.

• Reference NextSeq 1000/2000 Product Documentation.

HiSeq 2500

• Remove the clustered flow cell from the container using a pair of plastistats.

• Rinse the flow cell with laboratory-grade water. Dry with a lens cleaning tissue.

• Fold an alcohol wipe to approximately the size of the flow cell.

• Hold the edges of the flow cell with 2 fingers so that the inlet and outlet ports face up.

• Wipe each side of the flow cell using a single sweeping motion. Repeat until clean, refolding the alcohol wipe with each pass.

• Dry with a dry lens cleaning tissue.

• Protect the flow cell from dust until ready to load it onto the instrument.

• Reference: HiSeq 2500 System Guide.

HiSeq 3000/4000/X

• It is not necessary to clean the flow cell.

• If desired, can clean the glass surface of the flow cell with a lint-free alcohol wipe. Dry the glass with a low-lint lab tissue.

• Reference: HiSeq 3000 System Guide, HiSeq 4000 System Guide, HiSeq X System Guide.

NovaSeq 6000

• It is not necessary to clean the flow cell.

• If desired, clean the glass surface of the flow cell with a lint-free alcohol wipe. Dry the glass with a low-lint lab tissue.

• Reference: NovaSeq 6000 Sequencing System Guide.

For any feedback or questions regarding this article (Illumina Knowledge Article #5147), contact Illumina Technical Support [e-mail].