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L15b300 medium

Manufactured by Merck Group

L15B300 medium is a cell culture medium designed for the growth and maintenance of a variety of cell types. It provides the necessary nutrients and components to support cell proliferation and survival in vitro.

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2 protocols using l15b300 medium

1

Propagation and Infection of Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human neuroblastoma cells (SH-SY5Y; CRL-2266; American Type culture Collection: ATCC), and Ixodes scapularis tick embryonic (ISE6; NR12234; BEI Resources) cell lines were purchased from ATCC/BEI and propagated as per the instructions from the supplier. Human SH-SY5Y cells were grown in complete EMEM medium (ATCC recommended) with 10% heat-inactivated Fetal bovine serum (FBS) (SIGMA) at 37 °C and 5% CO2, respectively. ISE6 cells were cultured and grown in L15B300 medium (SIGMA) at 34 °C and as per the recommendations from Dr. Munderloh[50 (link),51 (link)]. Human skin keratinocytes (HaCaT cells) were obtained from Addexbio Technologies/FisherScientific and grown (as per the instructions from the supplier) in complete Dulbecco’s Modified Eagle Medium (DMEM; SIGMA) with 10% heat-inactivated FBS at 37 °C and 5% CO2. SH-SY5Y or ISE6 cells were plated at densities of 1–2 × 10e6, and after overnight incubations, cells were infected with Langat virus [LGTV, strain LGT-TP21, 1 MOI (multiplication of infection) for ISE6 cells or 5 MOI for SH-SY5Y cells]. Naïve SH-SY5Y or HaCaT cells were infected via infectious exosomes collected from either SH-SY5Y or tick cells, respectively.
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2

Propagation and Infection of Cell Lines

Check if the same lab product or an alternative is used in the 5 most similar protocols
Human neuroblastoma cells (SH-SY5Y; CRL-2266; American Type culture Collection: ATCC), and Ixodes scapularis tick embryonic (ISE6; NR12234; BEI Resources) cell lines were purchased from ATCC/BEI and propagated as per the instructions from the supplier. Human SH-SY5Y cells were grown in complete EMEM medium (ATCC recommended) with 10% heat-inactivated Fetal bovine serum (FBS) (SIGMA) at 37 °C and 5% CO2, respectively. ISE6 cells were cultured and grown in L15B300 medium (SIGMA) at 34 °C and as per the recommendations from Dr. Munderloh[50 (link),51 (link)]. Human skin keratinocytes (HaCaT cells) were obtained from Addexbio Technologies/FisherScientific and grown (as per the instructions from the supplier) in complete Dulbecco’s Modified Eagle Medium (DMEM; SIGMA) with 10% heat-inactivated FBS at 37 °C and 5% CO2. SH-SY5Y or ISE6 cells were plated at densities of 1–2 × 10e6, and after overnight incubations, cells were infected with Langat virus [LGTV, strain LGT-TP21, 1 MOI (multiplication of infection) for ISE6 cells or 5 MOI for SH-SY5Y cells]. Naïve SH-SY5Y or HaCaT cells were infected via infectious exosomes collected from either SH-SY5Y or tick cells, respectively.
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