Stratagene ViraPort cDNA Library Retroviral Supernatants Instruction Manual

This is an instruction manual for a product called ViraPort cDNA Library Retroviral Supernatants, which is produced by Agilent. The manual contains information on how to use the product, warranty terms and conditions, and more.


Stratagene ViraPort cDNA Library Retroviral Supernatants Instruction Manual - cover page
Brand
STRATAGENE
Document type
User Manual
Language
English
Pages
25
File format
PDF
File size
240 KB
Published
06 June, 2012
Updated
30 September, 2023
MD5 checksum
95D797D522AA6D1E1C38F0BD297DD489

About this manual

The document is an instruction manual for the ViraPort cDNA Library Retroviral Supernatants (BN #972000-12), produced by Stratagene. It details the materials provided with the kit, such as frozen tissue culture supernatant containing VSV-G pseudotyped retrovirus and lyophilized primers. The manual specifies storage conditions at -80°C for the supernatants and -20°C for primers.

What's inside

  • Materials Provided
  • Storage Conditions
  • Safety Considerations
  • Overview of Replication-Defective Retroviral Gene Transfer Systems
  • Description of the pFB Retroviral Vector
  • Determination of Target Cell Transduction Efficiency Using the pFB-hrGFP Control Viral Supernatant
  • Transduction of Target Cells with ViraPort cDNA Library Supernatant
  • Recovery of cDNA Clones from Positive Transductant
  • PCR Reaction
  • Troubleshooting

Specifications

Virus Titer (Supernatant)> 2 X 10^5 infectious virus particles
Primer Quantity (5' Retro primer)2.5 ug
Primer Quantity (3' pFB primer)2.5 ug
Virus Titer (Control Viral Supernatant)> 10^8 infectious virus particles
Filter Size0.45 um

Frequently asked questions

What is the recommended storage temperature for ViraPort Retroviral Supernatants?

The retroviral supernatant should be stored at -80°C immediately upon arrival.

What is the recommended storage temperature for the primers?

The lyophilized primers should be stored at -20°C.

How should the lyophilized primers be prepared for use in PCR?

Resuspend each primer in 25 ul of TE buffer to a final concentration of 100 ng/ul.

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