Characterization of Gracilaria lemaneiformis Bory (Gracilariaceae, Rhodophyta) cultivars in China using the total soluble proteins and RAPD analysis

2007 ◽  
Vol 50 (3) ◽  
Author(s):  
Wen-jun Wang ◽  
Guang-ce Wang ◽  
Zheng-quan Gao ◽  
Xiang-zhi Lin ◽  
Pu Xu
Keyword(s):  
Rapd Analysis ◽  
Soluble Proteins ◽  
Gracilaria Lemaneiformis

Characterization of active compounds from Gracilaria lemaneiformis inhibiting the protein tyrosine phosphatase 1B activity

2017 ◽  
Vol 8 (9) ◽  
pp. 3271-3275 ◽  
Author(s):  
Xinfeng Guo ◽  
Dongyu Gu ◽  
Miao Wang ◽  
Yu Huang ◽  
Haoquan Li ◽  
...  
Keyword(s):  
Protein Tyrosine Phosphatase ◽  
Tyrosine Phosphatase ◽  
Gracilaria Lemaneiformis ◽  
Protein Tyrosine Phosphatase 1B ◽  
Active Compounds ◽  
Protein Tyrosine

Gracilaria lemaneiformis, an edible alga, with various bioactivities is a traditional dish and a favorite food.

Characterization of the soluble proteins from rabbit eye lens

1974 ◽  
Vol 18 (2) ◽  
pp. 143-152 ◽  
Author(s):  
K.N. Liem-The ◽  
H.J. Hoenders
Keyword(s):  
Soluble Proteins ◽  
Eye Lens ◽  
Rabbit Eye

Molecular characterization of Desmodium species — An important ingredient of ‘Dashmoola’ by RAPD analysis

Fitoterapia ◽  
2009 ◽  
Vol 80 (2) ◽  
pp. 115-118 ◽  
Author(s):  
Saba Irshad ◽  
Jyotsna Singh ◽  
Poonam Kakkar ◽  
Shanta Mehrotra
Keyword(s):  
Molecular Characterization ◽  
Rapd Analysis ◽  
Important Ingredient

Characterization of chick lens soluble proteins and the control of their synthesis

1978 ◽  
Vol 26 (3) ◽  
pp. 351-362 ◽  
Author(s):  
Iain Thomson ◽  
Christine E. Wilkinson ◽  
Alan T.H. Burns ◽  
Donald E.S. Truman ◽  
Ruth M. Clayton
Keyword(s):  
Soluble Proteins ◽  
Chick Lens

scholarly journals 678 PB 186 RAPD GENETIC MARKERS FOR CHARACTERIZATION OF MUSA GENETIC RESOURCES

HortScience ◽  
1994 ◽  
Vol 29 (5) ◽  
pp. 530a-530
Author(s):  
R.L. Jarret ◽  
K.V. Bhat
Keyword(s):  
Genetic Markers ◽  
Size Range ◽  
Rapd Analysis ◽  
Random Amplified Polymorphic Dna ◽  
Dna Amplification ◽  
Principal Coordinate Analysis ◽  
Phenetic Analysis ◽  
Similarity Coefficients ◽  
Primer Sequence

Fifty-seven accessions of Musa including cultivated clones Of 6 genomic groups (AA, AB, AAA, AAB, ABB, ABBB), M. balbisiana (BB), M. acuminata ssp. banksii (AA), M. acuminata ssp. malaccensis (AA) and M. velutina were examined for random amplified polymorphic DNA (RAPD) genetic markers using PCR with sixty 10-mer random primers. Forty-nine of 60 tested primers gave reproducible DNA amplification patterns. The number of bands resolved per amplification was primer dependent and varied from 1 to a maximum of 24. The size range of the amolification products also differed with the select& primer sequence/genotype and ranged from 0.29 to 3.0 kb. RAPD data were used to generate Jaccard's similarity coefficients which were analyzed phenetically. Phenetic analysis separated clones into distinct groupings that were in agreement with clusterings revealed when data were subsequently analyzed by principal coordinate analysis (PCO). In both the phenetic and the PCO analyses, previously unclassified cultivars grouped with cultivars previously classified for their genomic group based on morphological keys. The implications of RAPD analysis for Musa germplasm classification, clonal identification, and management are discussed.

scholarly journals Use RAPD Technique for Characterization of Genotypical Variability of Maize Germplasm from SCDA Turda

2010 ◽  
Vol 67 (1) ◽  
Author(s):  
Rodica POP ◽  
Doru PAMFIL ◽  
Monica HÂRŢA ◽  
Ioan HAŞ ◽  
Iulia POP
Keyword(s):  
Rapd Markers ◽  
Rapd Analysis ◽  
Genetic Relationships ◽  
Germplasm Collection ◽  
Genetic Distances ◽  
Maize Germplasm ◽  
Upgma Dendrogram ◽  
Maize Genotypes ◽  
Polymorphic Bands

Genetic analysis with RAPD markers has been extensively used to determine diversity among maize genotypes. The aim of the present study was to estimate genetic relationships among 70 genotypes, provided from SCDA Turda Cluj germplasm collection. RAPD analysis was performed with 14 decamer primers. These primers generated, among the studied genotypes, a number of polymorphic bands comprised between 13 bands (OPA 04) and 7 bands (OPAL 20). The highest numbers of polymorphic bands were obtained with primer OPA 04, respectively 13 bands, following by OPO 12 (12 polymorphic bands), OPAB 11 and OPA 17 (11 polymorphic bands). Lowest number was obtained with primer OPAL 20, respectively 7 polymorphic bands. Genetic distances were established using Nei-Li coefficient and UPGMA dendrogram was constructed with RAPDistance 1.04 software. The built dendrogram shows phylogenetic relationships between genotypes analyzed.

scholarly journals Characterization of Chickpea (Cicer arietinum L.) Genotypes through RAPD Analysis

2020 ◽  
Vol 9 (11) ◽  
pp. 1366-1372
Author(s):  
S. K. Rajoriya ◽  
Arunabh Joshi ◽  
Devendra Jain ◽  
Amit Dadeech ◽  
Ganesh Rajamani ◽  
...  
Keyword(s):  
Cicer Arietinum ◽  
Rapd Analysis ◽  
Cicer Arietinum L

scholarly journals Characterization of Alstroemeria Species using Random Amplified Polymorphic DNA (RAPD) Analysis

HortScience ◽  
1997 ◽  
Vol 32 (3) ◽  
pp. 482F-482 ◽  
Author(s):  
Deric D. Picton ◽  
Harrison G. Hughes
Keyword(s):  
Rapd Analysis ◽  
Random Amplified Polymorphic Dna ◽  
Randomly Amplified Polymorphic Dna ◽  
Banding Patterns ◽  
Extraction Buffer ◽  
Rapd Pcr ◽  
High Degree ◽  
Species Hybrids ◽  
Color Variants

In this study, 11 species, hybrids, and color variants were characterized using randomly amplified polymorphic DNA (RAPD) analysis. Total genomic DNA was extracted using a 2% CTAB extraction buffer using fresh or frozen leaf material. The DNA was amplified using standard RAPD-PCR protocols utilizing 10-mer primers. All primers utilized exhibited a high degree of polymorphism in their banding patterns among the species and hybrids studied. The primers used produced ≈40 reproducible bands. It was possible to identify and uniquely distinguish all species and hybrids investigated using these bands.

Sign in / Sign up

Export Citation Format

Share Document