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Comparison of Reverse Transcription Quantitative Real-Time PCR, Flow Cytometry, and Immunohistochemi...

Comparison of Reverse Transcription Quantitative Real-Time PCR, Flow Cytometry, and Immunohistochemi...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_gup_ub_gu_se_235527

Comparison of Reverse Transcription Quantitative Real-Time PCR, Flow Cytometry, and Immunohistochemistry for Detection of Monoclonality in Lymphomas

About this item

Full title

Comparison of Reverse Transcription Quantitative Real-Time PCR, Flow Cytometry, and Immunohistochemistry for Detection of Monoclonality in Lymphomas

Publisher

Egypt: Hindawi Publishing Corporation

Journal title

ISRN oncology, 2014, Vol.2014, p.796210-6

Language

English

Formats

Publication information

Publisher

Egypt: Hindawi Publishing Corporation

More information

Scope and Contents

Contents

In healthy humans, 60–70% of the B lymphocytes produce kappa light chains, while the remaining cells produce lambda light chains. Malignant transformation and clonal expansion of B lymphocytes lead to an altered kappa : lambda expression ratio, which is an important diagnostic criteria of lymphomas. Here, we compared three methods for clonality det...

Alternative Titles

Full title

Comparison of Reverse Transcription Quantitative Real-Time PCR, Flow Cytometry, and Immunohistochemistry for Detection of Monoclonality in Lymphomas

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_swepub_primary_oai_gup_ub_gu_se_235527

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_swepub_primary_oai_gup_ub_gu_se_235527

Other Identifiers

ISSN

2090-5661,2090-567X

E-ISSN

2090-567X

DOI

10.1155/2014/796210

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