atcc 204304 reference strains Search Results


97
ATCC strains atcc 204304
Strains Atcc 204304, supplied by ATCC, used in various techniques. Bioz Stars score: 97/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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98
ATCC atcc reference strains
Atcc Reference Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 98/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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96
ATCC a flavus
Cultures and microscopic examinations of clinical isolates on SDA after 5 days at <t>37°C.</t> <t>PW2952</t> (A) and PW2955 (B) produced velvety colonies with floccose tufts and yellowish green conidia. (C) PW2958 produced dark green-brown conidia at maturity and formed velutinous colonies with floccose tufts. The conidiophores of PW2952 (D) and PW2955 (E) were hyaline, with globose to subglobose vesicles and biseriate phialides. (F) The conidiophores of PW2958 were hyaline, with globose vesicles and biseriate phialides producing brownish-yellow conidia.
A Flavus, supplied by ATCC, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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99
ATCC control strains
Cultures and microscopic examinations of clinical isolates on SDA after 5 days at <t>37°C.</t> <t>PW2952</t> (A) and PW2955 (B) produced velvety colonies with floccose tufts and yellowish green conidia. (C) PW2958 produced dark green-brown conidia at maturity and formed velutinous colonies with floccose tufts. The conidiophores of PW2952 (D) and PW2955 (E) were hyaline, with globose to subglobose vesicles and biseriate phialides. (F) The conidiophores of PW2958 were hyaline, with globose vesicles and biseriate phialides producing brownish-yellow conidia.
Control Strains, supplied by ATCC, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Cultures and microscopic examinations of clinical isolates on SDA after 5 days at 37°C. PW2952 (A) and PW2955 (B) produced velvety colonies with floccose tufts and yellowish green conidia. (C) PW2958 produced dark green-brown conidia at maturity and formed velutinous colonies with floccose tufts. The conidiophores of PW2952 (D) and PW2955 (E) were hyaline, with globose to subglobose vesicles and biseriate phialides. (F) The conidiophores of PW2958 were hyaline, with globose vesicles and biseriate phialides producing brownish-yellow conidia.

Journal: Journal of Clinical Microbiology

Article Title: Misidentification of Aspergillus nomius and Aspergillus tamarii as Aspergillus flavus : Characterization by Internal Transcribed Spacer, β-Tubulin, and Calmodulin Gene Sequencing, Metabolic Fingerprinting, and Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry

doi: 10.1128/JCM.03258-13

Figure Lengend Snippet: Cultures and microscopic examinations of clinical isolates on SDA after 5 days at 37°C. PW2952 (A) and PW2955 (B) produced velvety colonies with floccose tufts and yellowish green conidia. (C) PW2958 produced dark green-brown conidia at maturity and formed velutinous colonies with floccose tufts. The conidiophores of PW2952 (D) and PW2955 (E) were hyaline, with globose to subglobose vesicles and biseriate phialides. (F) The conidiophores of PW2958 were hyaline, with globose vesicles and biseriate phialides producing brownish-yellow conidia.

Article Snippet: The three-dimensional (3D) PCA score plot revealed that the nine strains of A. flavus (PW2952, PW2953, PW2954, PW2956, PW2957, PW2960, PW2961, PW2962, and ATCC 204304), the three strains of A. nomius (PW2955, PW2959, and CBS260.88 T ), and the two strains of A. tamarii (PW2958 and CBS104.13 T ) can be distinguished from each other, but strains within the same species are closely related.

Techniques: Produced

Fungal isolates reported as  A. flavus  and control strains used in the present study

Journal: Journal of Clinical Microbiology

Article Title: Misidentification of Aspergillus nomius and Aspergillus tamarii as Aspergillus flavus : Characterization by Internal Transcribed Spacer, β-Tubulin, and Calmodulin Gene Sequencing, Metabolic Fingerprinting, and Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry

doi: 10.1128/JCM.03258-13

Figure Lengend Snippet: Fungal isolates reported as A. flavus and control strains used in the present study

Article Snippet: The three-dimensional (3D) PCA score plot revealed that the nine strains of A. flavus (PW2952, PW2953, PW2954, PW2956, PW2957, PW2960, PW2961, PW2962, and ATCC 204304), the three strains of A. nomius (PW2955, PW2959, and CBS260.88 T ), and the two strains of A. tamarii (PW2958 and CBS104.13 T ) can be distinguished from each other, but strains within the same species are closely related.

Techniques: Sequencing

(A) Principal component analysis and (B) hierarchical clustering dendrogram of metabolic fingerprints of the 11 clinical isolates reported as A. flavus and three reference strains. Molecular features (1,016) defined by retention time and mass pair were included. The 3D PCA score plot for component PC1 versus component PC2 versus component PC3 is presented. The percentages of variance in the data set reflected by the first three PCs for each sample are shown. Hierarchical clustering of different fungal isolates is represented by a heat map and a dendrogram. Clustering was performed using Euclidean distance and average linkage. Blue and red indicate negative and positive log ratios, respectively. Two biological replicates were performed for each sample. Lanes 1 and 2, PW2952; lanes 3 and 4, PW2956; lanes 5 and 6, PW2957; lanes 7 and 8, PW2960; lanes 9 and 10, PW2962; lanes 11 and 12, ATCC 204304; lanes 13 and 14, PW2953; lanes 15 and 16, PW2954; lanes 17 and 18, PW2961; lanes 19 and 20, CBS260.88T; lanes 21 and 22, PW2955; lanes 23 and 24, PW2959; lanes 25 and 26, CBS104.13T; lanes 27 and 28, PW2958.

Journal: Journal of Clinical Microbiology

Article Title: Misidentification of Aspergillus nomius and Aspergillus tamarii as Aspergillus flavus : Characterization by Internal Transcribed Spacer, β-Tubulin, and Calmodulin Gene Sequencing, Metabolic Fingerprinting, and Matrix-Assisted Laser Desorption Ionization–Time of Flight Mass Spectrometry

doi: 10.1128/JCM.03258-13

Figure Lengend Snippet: (A) Principal component analysis and (B) hierarchical clustering dendrogram of metabolic fingerprints of the 11 clinical isolates reported as A. flavus and three reference strains. Molecular features (1,016) defined by retention time and mass pair were included. The 3D PCA score plot for component PC1 versus component PC2 versus component PC3 is presented. The percentages of variance in the data set reflected by the first three PCs for each sample are shown. Hierarchical clustering of different fungal isolates is represented by a heat map and a dendrogram. Clustering was performed using Euclidean distance and average linkage. Blue and red indicate negative and positive log ratios, respectively. Two biological replicates were performed for each sample. Lanes 1 and 2, PW2952; lanes 3 and 4, PW2956; lanes 5 and 6, PW2957; lanes 7 and 8, PW2960; lanes 9 and 10, PW2962; lanes 11 and 12, ATCC 204304; lanes 13 and 14, PW2953; lanes 15 and 16, PW2954; lanes 17 and 18, PW2961; lanes 19 and 20, CBS260.88T; lanes 21 and 22, PW2955; lanes 23 and 24, PW2959; lanes 25 and 26, CBS104.13T; lanes 27 and 28, PW2958.

Article Snippet: The three-dimensional (3D) PCA score plot revealed that the nine strains of A. flavus (PW2952, PW2953, PW2954, PW2956, PW2957, PW2960, PW2961, PW2962, and ATCC 204304), the three strains of A. nomius (PW2955, PW2959, and CBS260.88 T ), and the two strains of A. tamarii (PW2958 and CBS104.13 T ) can be distinguished from each other, but strains within the same species are closely related.

Techniques: