FAQ Database - Complete List

350 FAQ articles available.

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81. Four hours after Nucleofection®, I can see the hepatocytes have attached to the well, but the morphology does not look correct, should I be concerned?

82. As hepatocytes are a very large cell type, should I be worried about Nucleofection® causing cell fusions?

83. What is the average yield of hepatocytes post Nucleofection®?

84. I followed the protocol, but I observed low viability with my hepatocytes. What should I do?

85. Is it more difficult to detect DsRed by FACS than GFP?

86. What kind of suspension CHO cells did you use for protein production?

87. Can I use the pmaxGFP® control plasmid with insect cells such as S2 cells or SF9 cells?

88. Do you have any information regarding differentiation of mouse ES cells after Nucleofection® with large plasmids?

89. Does the Mouse T cell protocol work for stimulated mouse T cells?

90. Is it possible to transfect proteins using the Nucleofector® technology?

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