Theileria parva PCR detection kit, Camel, DNA
- Known as:
- Theileria parva PCR test kit quantification reagent, Camel, Desoxyribonucleic acid
- Catalog number:
- VET-CA003-96D
- Product Quantity:
- 48rxs
- Category:
- -
- Supplier:
- Bioinge
- Gene target:
- Theileria parva PCR detection kit Camel DNA
Related genes to: Theileria parva PCR detection kit, Camel, DNA
- Gene:
- PARVA NIH gene
- Name:
- parvin alpha
- Previous symbol:
- MXRA2
- Synonyms:
- FLJ12254, FLJ10793
- Chromosome:
- 11p15.3
- Locus Type:
- gene with protein product
- Date approved:
- 2001-04-26
- Date modifiied:
- 2018-03-02
Related products to: Theileria parva PCR detection kit, Camel, DNA
Related articles to: Theileria parva PCR detection kit, Camel, DNA
- Ticks are important vectors for bacterial, viral, rickettsial, and protozoal diseases in different animals and humans, especially in tropical countries. Tick-borne pathogens (TBPs) are host and vector-species-specific and depict geographical variations. This study was conducted to determine the diversity of ticks and their geographical distribution among domestic animals. - Source: PubMed
Publication date: 2026/06/08
Thapa KamanaPathak Chet RajAryal SomnathKanu Surendra Prasad - Chlorophycean algae of the genera Chlamydomonas and Polytomella share a common photosynthetic ancestor. However, members of the Polytomella lineage have adopted a heterotrophic lifestyle, having lost the photosynthetic apparatus and relying instead on acetate or ethanol as carbon sources, with energy production centered on oxidative phosphorylation (OXPHOS). In this study, we investigated the composition of the mitochondrial supercomplexes of the colorless alga Polytomella parva. Mitochondrial membranes were solubilized using mild detergents such as glycol-diosgenin and digitonin, followed by separation of OXPHOS complexes supramolecular assemblies via Blue Native electrophoresis and Fast Protein Liquid Chromatography (FPLC). Additionally, complexome profiling of solubilized algal mitochondria resolved by Blue Native Gel Electrophoresis was carried out (data are available via ProteomeXchange with identifier PXD075371). The resulting data indicate that the OXPHOS supercomplexes of Polytomella closely resemble those observed in situ in the mitochondria of its green relative Chlamydomonas reinhardtii, as revealed by electron cryo-tomography and subtomogram averaging. - Source: PubMed
Publication date: 2026/05/07
Ostolga-Chavarría MarcosRico-Luna AnaizaFuentes-Hernández SergioMiranda-Astudillo Héctor VCabrera-Orefice AlfredoGonzález-Halphen Diego - Understanding the migration pathways of microplastics (MPs) in freshwater ecosystems and their associated risks to aquatic reproductive health is critically needed. This study investigated these processes in Baiyangdian, a typical large shallow lake. MPs were analyzed in water, sediment, and intestines from two habitat-differentiated fish species-the benthic Carassius auratus and the water column-dwelling Pseudorasbora parva. Across all compartments, 31 polymer types were identified, with 20 common to all media. Small particles (< 100 μm) were significantly more abundant than large ones (> 100 μm) in each compartment. Principal coordinates analysis (PCoA) and SourceTracker indicated that there was no significant difference between MPs in C. auratus intestines and those in sediment, and the proportion of intestinal MPs derived from sediment was significantly higher than that from the water column (P < 0.05). MPs in P. parva intestines differed significantly from both water and sediment, with the majority (> 80%) attributed to unassigned sources. Boosted Regression Trees (BRT) analyses revealed species-specific patterns: sediment and intestinal MPs showed higher relative importance for reproductive parameters in C. auratus, and water and intestinal MPs in P. parva. Multiple Linear Regression (MLR) identified specific polymers as key risk factors, with effect directions largely consistent with the overall medium-level associations identified by BRT. Integrating multivariate statistical and modeling approaches, this study characterizes MP transfer from environmental compartments to fish and assesses associations with reproductive parameters under field conditions. These findings underscore the necessity of incorporating pollutant sources and biological exposure pathways into ecological risk assessment frameworks. - Source: PubMed
Publication date: 2026/05/25
Qiao YanzhenWang YaguangYang BoliangZhang XiaoyuWan HaifuCui XiaodongXu YangShen YifanGuan YueqiangKang Xianjiang - Tamdy virus (TAMV) is an emerging tick-borne virus in the family Nairoviridae, identified as a human pathogen causing febrile illness after tick exposure. This study aimed to detect and characterise TAMV in ticks collected from non-endemic regions of Türkiye. A total of 529 ticks were sampled from six provinces and identified as Haemaphysalis parva (27%), Rhipicephalus bursa (26%), Haemaphysalis punctata (20.7%), Dermacentor marginatus (17.2%), and Ixodes ricinus (8.8%). Screening with a single-step generic PCR revealed one TAMV-positive pool out of 96. For characterisation, the S segment of TAMV was amplified using two primer sets. Phylogenetic analyses of the partial L gene and full S segment showed that the sequence from Osmaniye sample clustered closely with the TT1 isolate from Konya, Türkiye. Amino acid comparison indicated that Turkish isolates were more similar to each other than to those from Russia and China, forming a distinct clade within TAMV. Minor amino acid differences between the Turkish isolates suggest that TAMV diversity in Türkiye is shaped by internal evolution rather than external introductions. These findings highlight the importance of continuous surveillance of tick-borne zoonotic viruses and suggest that TAMV may have a wider vector range and geographic distribution than previously recognised. - Source: PubMed
Publication date: 2026/05/25
Dincer EnderTimurkan Mehmet Ozkan - Effective vaccines are essential to overcome the limitations of livestock immunisation, particularly in low- and middle-income countries (LMICs), where scalable, thermostable, and easy-to-administer solutions are needed. Nanoparticle-based delivery systems, such as the Spontaneous Nanoliposome Antigen Particle (SNAP) technology using CoPoP liposomes, offer a promising alternative for subunit vaccine development, although their performance in large animal species remains poorly characterised. CoPoP enables the rapid non-covalent multimeric display of His-tagged protein antigens combined with immunomodulators on liposomes incorporating cobalt porphyrin-phospholipid (CoPoP). To evaluate the immunogenicity of CoPoP-based liposomes delivering the p67C antigen in cattle and compare their performance in murine models. Cattle and mice were immunised with p67C formulated in CoPoP liposomes incorporating QS-21 and/or PHAD immunomodulators. Humoral and cellular responses were assessed. Parallel in vitro stimulation of bovine PBMC with Quil-A was used to investigate the mechanistic effects of saponins on bovine cells. CoPoP liposome formulations did not improve p67C immunogenicity in cattle, with antibody responses at least two-fold lower than previously reported results and no detectable cellular responses. In contrast, the same platform induced up to 2000-fold higher antibody titres in mice. This disparity is likely driven by differences in antigen dose relative to body mass, tissue architecture, lymphatic accessibility, and innate immune signalling differences. PHAD-mediated TLR4 activation appeared less effective in cattle, whereas QS-21 induced a broader immune activation, likely through conserved inflammasome pathways. Despite limited immunogenicity, antigen presentation by CoPoP liposomes was preserved. SNAP-based CoPoP liposomes showed strong immunogenicity in mice but limited efficacy in cattle, highlighting the challenges of cross-species translation. Optimisation of antigen dose and adjuvant selection for the targeted species is required, with QS-21 representing a more promising candidate than the TLR4 agonist. The scalability and versatility of SNAP technology support its continued development for multivalent livestock vaccines. - Source: PubMed
Publication date: 2026/05/20
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