Detection of Del Phenotype in RH negative blood by using chloroform elution technique and specific sequence Primer-Polymerase Chain Reaction (SSP-PCR) / Nor Arina Che Mohd Noor

DEL phenotype is known as the weakest D antigen in the Rh blood group system. Serologically, DEL phenotype commonly mistyped as true Rh negative. An anti-D immunization may occurred in Rh negative recipient who received blood from the DEL phenotype donor. The goals of the present study were to detec...

Full description

Bibliographic Details
Main Author: Che Mohd Noor, Nor Arina
Format: Thesis
Language:English
Published: 2015
Subjects:
Online Access:https://ir.uitm.edu.my/id/eprint/28026/1/TD_NOR%20ARINA%20CHE%20MOHD%20NOOR%20HS%2015_5.pdf
_version_ 1825736765201186816
author Che Mohd Noor, Nor Arina
author_facet Che Mohd Noor, Nor Arina
author_sort Che Mohd Noor, Nor Arina
collection UITM
description DEL phenotype is known as the weakest D antigen in the Rh blood group system. Serologically, DEL phenotype commonly mistyped as true Rh negative. An anti-D immunization may occurred in Rh negative recipient who received blood from the DEL phenotype donor. The goals of the present study were to detect DEL phenotype in Rh negative blood by using chloroform elution technique and specific sequence primer-polymerase chain reaction (SSP-PCR). A total of 43 Rh negative blood donor's samples from National Blood Centre were examined for the Rh phenotyping and the presence of DEL phenotype by using chloroform elution technique and SSPPCR. The Rh negative phenotypes consisted of 79.07% dce, 13.95% dCce, 4.65% dcEe and 2.33% dCe. Chloroform elution technique failed to detect DEL phenotype, but only 2.33% (1/43) Rh negative blood donor's sample was being detected as DEL phenotype by using SSP-PCR. In conclusion, based on these findings, chloroform elution technique might not be an effective method in detection of DEL phenotype. Sensitivity and specificity of molecular typing method can overcome the limitation of serological method in the clinical laboratory. Hence, it is highly recommended to use SSP-PCR in detection of DEL phenotype in Rh negative blood, thus preventing the anti-D immunization.
first_indexed 2024-03-06T02:07:39Z
format Thesis
id uitm.eprints-8026
institution Universiti Teknologi MARA
language English
last_indexed 2024-03-06T02:07:39Z
publishDate 2015
record_format dspace
spelling uitm.eprints-80262020-02-04T08:57:25Z https://ir.uitm.edu.my/id/eprint/28026/ Detection of Del Phenotype in RH negative blood by using chloroform elution technique and specific sequence Primer-Polymerase Chain Reaction (SSP-PCR) / Nor Arina Che Mohd Noor Che Mohd Noor, Nor Arina Clinical pathology. Laboratory technique Examination of the blood DEL phenotype is known as the weakest D antigen in the Rh blood group system. Serologically, DEL phenotype commonly mistyped as true Rh negative. An anti-D immunization may occurred in Rh negative recipient who received blood from the DEL phenotype donor. The goals of the present study were to detect DEL phenotype in Rh negative blood by using chloroform elution technique and specific sequence primer-polymerase chain reaction (SSP-PCR). A total of 43 Rh negative blood donor's samples from National Blood Centre were examined for the Rh phenotyping and the presence of DEL phenotype by using chloroform elution technique and SSPPCR. The Rh negative phenotypes consisted of 79.07% dce, 13.95% dCce, 4.65% dcEe and 2.33% dCe. Chloroform elution technique failed to detect DEL phenotype, but only 2.33% (1/43) Rh negative blood donor's sample was being detected as DEL phenotype by using SSP-PCR. In conclusion, based on these findings, chloroform elution technique might not be an effective method in detection of DEL phenotype. Sensitivity and specificity of molecular typing method can overcome the limitation of serological method in the clinical laboratory. Hence, it is highly recommended to use SSP-PCR in detection of DEL phenotype in Rh negative blood, thus preventing the anti-D immunization. 2015 Thesis NonPeerReviewed text en https://ir.uitm.edu.my/id/eprint/28026/1/TD_NOR%20ARINA%20CHE%20MOHD%20NOOR%20HS%2015_5.pdf Detection of Del Phenotype in RH negative blood by using chloroform elution technique and specific sequence Primer-Polymerase Chain Reaction (SSP-PCR) / Nor Arina Che Mohd Noor. (2015) Degree thesis, thesis, Universiti Teknologi MARA. <http://terminalib.uitm.edu.my/28026.pdf>
spellingShingle Clinical pathology. Laboratory technique
Examination of the blood
Che Mohd Noor, Nor Arina
Detection of Del Phenotype in RH negative blood by using chloroform elution technique and specific sequence Primer-Polymerase Chain Reaction (SSP-PCR) / Nor Arina Che Mohd Noor
title Detection of Del Phenotype in RH negative blood by using chloroform elution technique and specific sequence Primer-Polymerase Chain Reaction (SSP-PCR) / Nor Arina Che Mohd Noor
title_full Detection of Del Phenotype in RH negative blood by using chloroform elution technique and specific sequence Primer-Polymerase Chain Reaction (SSP-PCR) / Nor Arina Che Mohd Noor
title_fullStr Detection of Del Phenotype in RH negative blood by using chloroform elution technique and specific sequence Primer-Polymerase Chain Reaction (SSP-PCR) / Nor Arina Che Mohd Noor
title_full_unstemmed Detection of Del Phenotype in RH negative blood by using chloroform elution technique and specific sequence Primer-Polymerase Chain Reaction (SSP-PCR) / Nor Arina Che Mohd Noor
title_short Detection of Del Phenotype in RH negative blood by using chloroform elution technique and specific sequence Primer-Polymerase Chain Reaction (SSP-PCR) / Nor Arina Che Mohd Noor
title_sort detection of del phenotype in rh negative blood by using chloroform elution technique and specific sequence primer polymerase chain reaction ssp pcr nor arina che mohd noor
topic Clinical pathology. Laboratory technique
Examination of the blood
url https://ir.uitm.edu.my/id/eprint/28026/1/TD_NOR%20ARINA%20CHE%20MOHD%20NOOR%20HS%2015_5.pdf
work_keys_str_mv AT chemohdnoornorarina detectionofdelphenotypeinrhnegativebloodbyusingchloroformelutiontechniqueandspecificsequenceprimerpolymerasechainreactionssppcrnorarinachemohdnoor