L rahbarnia - Academia.edu (original) (raw)

L rahbarnia

I am an assistant professor of medical biotechnology in medical university of Tabriz,Iran.

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Papers by L rahbarnia

Research paper thumbnail of Tongue carcinoma: Case series and demographic analysis

Journal of Analytical Research in Clinical Medicine, Jul 25, 2013

Research paper thumbnail of Application of DsbA Signal Peptide for Soluble Expression of Leishmania infantum P4 Nuclease in E. coli

Asian Journal of Animal and Veterinary Advances, 2012

Research paper thumbnail of Molecular Cloning and Characterization of P4 Nuclease from Leishmania infantum

Enzyme Research, 2011

Parasite of the genusLeishmaniais reliant on the salvage pathway for recycling of ribonucleotides... more Parasite of the genusLeishmaniais reliant on the salvage pathway for recycling of ribonucleotides. A class I nuclease enzyme also known as P4 nuclease is involved in salvage of purines in cutaneous Leishmania species but the relevant enzymes have not been characterized inLeishmania infantum(L. infantum). The aim of this study was to clone and characterize the gene encoding class I nuclease inL. infantum. DNA extracted fromL. infantumwas used for amplification of P4 nuclease gene (Li-P4) by PCR. The product was cloned, sequenced, and expressed inE. colifor further characterization. Analysis of the sequence of Li-P4 revealed that the gene consists of an ORF of 951 bp. Sequence similarity analysis indicated that Li-P4 has a high homology to relevant enzymes of other kintoplastids with the highest homology (88%) to p1/s1 class I nuclease fromL. donovani. Western blotting of antirecombinant Li-P4 with promastigote and amastigote stages ofL. infantumshowed that this nuclease is present in...

Research paper thumbnail of Comparative Evaluation of Nested Polymerase Chain Reaction for Rapid Diagnosis of Human Brucellosis

Archives of Razi Institute, 2021

Brucellosis is recognized as a zoonotic disease with high morbidity in the absence of treatment. ... more Brucellosis is recognized as a zoonotic disease with high morbidity in the absence of treatment. The primary diagnosis of brucellosis can be effective in the achievement of satisfying treatment results and prevention of chronic infections. The present study aimed to compare the efficiency of conventional microbiological and serological approaches with nested Polymerase chain reaction (nested PCR) for rapid diagnosis of human brucellosis. A total of 120 subjects with symptoms of brucellosis were included in the study. The sensitivity and specificity of nested PCR for the detection of Brucella bacteria were compared with serological and blood culture methods. Out of 120 patients enrolled, brucellosis was detected in 73 (60.83%) cases based on serological tests with a blood culture confirmation in 8.33% of participants. Based on the obtained results, 55% of cases were positive in serum agglutination test (SAT≥1:160), and Coombs (C-SAT≥1:160) tests. Furthermore, seven negative SAT cases...

Research paper thumbnail of Purification and Immunological Characterization Evaluation of Recombinant Exotoxin A (Domains I, II) Protein isolated from Pseudomonas Aeruginosa

Research paper thumbnail of Isolation of human SCFV antibody against EGFR L2 domain by screening of human SCFV phage library

Research paper thumbnail of Tongue carcinoma: Case series and demographic analysis

Journal of Analytical Research in Clinical Medicine, Jul 25, 2013

Research paper thumbnail of Application of DsbA Signal Peptide for Soluble Expression of Leishmania infantum P4 Nuclease in E. coli

Asian Journal of Animal and Veterinary Advances, 2012

Research paper thumbnail of Molecular Cloning and Characterization of P4 Nuclease from Leishmania infantum

Enzyme Research, 2011

Parasite of the genusLeishmaniais reliant on the salvage pathway for recycling of ribonucleotides... more Parasite of the genusLeishmaniais reliant on the salvage pathway for recycling of ribonucleotides. A class I nuclease enzyme also known as P4 nuclease is involved in salvage of purines in cutaneous Leishmania species but the relevant enzymes have not been characterized inLeishmania infantum(L. infantum). The aim of this study was to clone and characterize the gene encoding class I nuclease inL. infantum. DNA extracted fromL. infantumwas used for amplification of P4 nuclease gene (Li-P4) by PCR. The product was cloned, sequenced, and expressed inE. colifor further characterization. Analysis of the sequence of Li-P4 revealed that the gene consists of an ORF of 951 bp. Sequence similarity analysis indicated that Li-P4 has a high homology to relevant enzymes of other kintoplastids with the highest homology (88%) to p1/s1 class I nuclease fromL. donovani. Western blotting of antirecombinant Li-P4 with promastigote and amastigote stages ofL. infantumshowed that this nuclease is present in...

Research paper thumbnail of Comparative Evaluation of Nested Polymerase Chain Reaction for Rapid Diagnosis of Human Brucellosis

Archives of Razi Institute, 2021

Brucellosis is recognized as a zoonotic disease with high morbidity in the absence of treatment. ... more Brucellosis is recognized as a zoonotic disease with high morbidity in the absence of treatment. The primary diagnosis of brucellosis can be effective in the achievement of satisfying treatment results and prevention of chronic infections. The present study aimed to compare the efficiency of conventional microbiological and serological approaches with nested Polymerase chain reaction (nested PCR) for rapid diagnosis of human brucellosis. A total of 120 subjects with symptoms of brucellosis were included in the study. The sensitivity and specificity of nested PCR for the detection of Brucella bacteria were compared with serological and blood culture methods. Out of 120 patients enrolled, brucellosis was detected in 73 (60.83%) cases based on serological tests with a blood culture confirmation in 8.33% of participants. Based on the obtained results, 55% of cases were positive in serum agglutination test (SAT≥1:160), and Coombs (C-SAT≥1:160) tests. Furthermore, seven negative SAT cases...

Research paper thumbnail of Purification and Immunological Characterization Evaluation of Recombinant Exotoxin A (Domains I, II) Protein isolated from Pseudomonas Aeruginosa

Research paper thumbnail of Isolation of human SCFV antibody against EGFR L2 domain by screening of human SCFV phage library

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