Development of a quantitative cell-based intracellular ELISA for the screening of B cell hybridoma supernatants: A novel rapid assay to detect positive clones

J. Gourapura Renukaradhya, Venkataraman Sriram, Katarina Polakova, Gustav Russ, Randy R. Brutkiewicz

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

The primary screening of hybridoma clones secreting monoclonal antibodies (MAbs) requires the testing of a large number of hybridoma culture supernatants within a short time and is very labor-intensive. In addition, the type of antigen and its location in the cell have to be considered when selecting the appropriate screening procedure, but relatively few reagents are available for analyzing these molecules. We have developed an intracellular and cell surface ELISA technique for screening hybridoma supernatants that hastens the screening procedure of a large number of clones in a short period of time, as the supernatants of fused cells grown in 96-well plates are used directly in the assay. This novel screening technique is rapid, sensitive, specific, and applicable to MAbs specific for a wide variety of intracellular and/or cell surface proteins.

Original languageEnglish (US)
Pages (from-to)373-379
Number of pages7
JournalHybridoma and Hybridomics
Volume23
Issue number6
DOIs
StatePublished - Dec 1 2004

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Hybridomas
B-Lymphocytes
Clone Cells
Enzyme-Linked Immunosorbent Assay
Monoclonal Antibodies
Membrane Proteins
Antigens

ASJC Scopus subject areas

  • Immunology
  • Genetics

Cite this

Development of a quantitative cell-based intracellular ELISA for the screening of B cell hybridoma supernatants : A novel rapid assay to detect positive clones. / Renukaradhya, J. Gourapura; Sriram, Venkataraman; Polakova, Katarina; Russ, Gustav; Brutkiewicz, Randy R.

In: Hybridoma and Hybridomics, Vol. 23, No. 6, 01.12.2004, p. 373-379.

Research output: Contribution to journalArticle

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