Sequencing and Characterisation of Complete Mitochondrial DNA
BCAS2, a protein enriched in superior prostate most cancers, interacts with NBS1 to reinforce DNA double-strand break restore
Background: Breast most cancers amplified sequence 2 (BCAS2) performs essential roles in pre-mRNA splicing and androgen receptor transcription. Earlier research urged that BCAS2 is concerned in double-strand breaks (DSB); due to this fact, we aimed to characterise its mechanism and position in prostate most cancers (PCa).
Strategies: Western blotting and immunofluorescence microscopy have been used to assay the roles of BCAS2 within the DSBs of PCa cells and apoptosis in Drosophila, respectively. The impact of BCAS2 dosage on non-homologous finish becoming a member of (NHEJ) and homologous recombination (HR) have been assayed by exact end-joining assay and move cytometry, respectively. Glutathione-S-transferase pulldown and co-immunoprecipitation assays have been used to find out whether or not and the way BCAS2 interacts with NBS1. The expression of BCAS2 and different proteins in human PCa was decided by immunohistochemistry.
Outcomes: BCAS2 helped restore radiation-induced DSBs effectively in each human PCa cells and Drosophila. BCAS2 enhanced each NHEJ and HR, probably by interacting with NBS1, which concerned the BCAS2 N-terminus as effectively as each the NBS1 N- and C-termini. The overexpression of BCAS2 was considerably related to larger Gleason and pathology grades and shorter survival in sufferers with PCa.
Conclusion: BCAS2 promotes two DSB restore pathways by interacting with NBS1, and it could have an effect on PCa development.
Description: A polyclonal antibody for detection of CSP from Human, Mouse, Rat. This CSP antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human CSP at AA range: 100-180
Description: A polyclonal antibody for detection of CSP from Human, Mouse, Rat. This CSP antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human CSP at AA range: 100-180
Description: A polyclonal antibody for detection of CSP from Human, Mouse, Rat. This CSP antibody is for WB, ELISA. It is affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogenand is unconjugated. The antibody is produced in rabbit by using as an immunogen synthesized peptide derived from the C-terminal region of human CSP at AA range: 100-180
Description: A polyclonal antibody raised in Rabbit that recognizes and binds to Human CSP . This antibody is tested and proven to work in the following applications:
Description: A polyclonal antibody raised in Goat that recognizes and binds to Human DNAJC5 / CSP (aa177-191). This antibody is tested and proven to work in the following applications:
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined.
Description: This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is highly expressed in brain and heart. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. One of the isoforms (known as ARTS) is distinct; it is localized to the mitochondria, and has a role in apoptosis and cancer.
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced.
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Description: This gene encodes a guanine-nucleotide binding protein and member of the septin family of cytoskeletal GTPases. Septins play important roles in cytokinesis, exocytosis, embryonic development, and membrane dynamics. Multiple transcript variants encoding different isoforms have been found for this gene.
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19.
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced.
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012]
(NANP)5 peptide (25-aa, repeat-sequence peptide of the P. falciparum circumsporozoite protein, CSP) conjugated with BSA
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids.
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids.
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids.
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit
Description: This is Competitive Enzyme-linked immunosorbent assay for Antibody Detection.detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in serum, plasma and other biological fluids.
Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) ELISA Kit
Description: Enzyme-linked immunosorbent assay based on the Competitive Inhibition method for detection of Human Anti-Anti-Sperm Antibody Antibody (Anti-AsAb) in samples from serum, plasma and other biological fluids with no significant corss-reactivity with analogues from other species.
Custom Testing of Samples for Antibodies (IgA/IgG/IgM) to Malaria Proteins (CSP/MSP-1/MSP-2/DBL5/VAR2CSA) by ELISA
Description: A competitive Inhibition ELISA kit for detection of Anti-Anti-Sperm Antibody Antibody from Human in samples from blood, serum, plasma, cell culture fluid and other biological fluids.
Sequencing and Characterisation of Complete Mitochondrial DNA Genome for Trigonopoma pauciperforatum (Cypriniformes: Cyprinidae: Danioninae) with Phylogenetic Consideration
The Trigonopoma pauciperforatum or the redstripe rasbora is a cyprinid generally present in marshes and swampy areas with slight acidic tannin-stained water within the tropics. On this research, the whole mitogenome sequence of pauciperforatum was first amplified in two components utilizing two pairs of overlapping primers after which sequenced.
The dimensions of the mitogenome is 16,707 bp, encompassing 22 switch RNA genes, 13 protein-coding genes, two ribosomal RNA genes and a putative management area. An identical gene organisation was detected between this species and different members of the family.
The heavy strand accommodates 28 genes whereas the sunshine strand homes the remaining 9 genes. Most protein-coding genes utilise ATG as begin codon aside from COI gene which makes use of GTG as an alternative. The terminal related sequence (TAS), central conserved sequence block (CSB-F, CSB-D and CSB-E) in addition to variable sequence block (CSB-1, CSB-2 and CSB-3) are conserved within the management area.
The utmost probability phylogenetic tree revealed the divergence of pauciperforatum from the basal area of the foremost clade, the place its evolutionary relationships with Boraras maculatus, Rasbora cephalotaenia and R. daniconius are poorly resolved as urged by the low bootstrap values.
This work contributes in the direction of the genetic useful resource enrichment for peat swamp conservation and complete in-depth comparisons throughout different phylogenetic researches completed on the Rasbora-related genus.
Reconstructing double-stranded DNA fragments on a single-molecule degree reveals patterns of degradation in historic samples
Intensive manipulations concerned within the preparation of DNA samples for sequencing have hitherto made it unimaginable to find out the exact construction of double-stranded DNA fragments being sequenced, such because the presence of blunt ends, single-stranded overhangs, or single-strand breaks.
We right here describe MatchSeq, a technique that mixes single-stranded DNA library preparation from diluted DNA samples with computational sequence matching, permitting the reconstruction of double-stranded DNA fragments on a single-molecule degree.
The appliance of MatchSeq to Neanderthal DNA, a very advanced supply of degraded DNA, reveals that 1- or 2-nt overhangs and blunt ends dominate the ends of historic DNA molecules and that brief gaps exist, that are predominantly brought on by the lack of particular person purines.
We additional present that deamination of cytosine to uracil happens in each single- and double-stranded contexts near the ends of molecules, and that single-stranded components of DNA fragments are enriched in pyrimidines. MatchSeq supplies unprecedented decision for interrogating the buildings of fragmented double-stranded DNA and could be utilized to fragmented double-stranded DNA remoted from any organic supply. The tactic depends on well-established laboratory methods and might simply be built-in into routine knowledge era.
This risk is proven by the profitable reconstruction of double-stranded DNA fragments from beforehand revealed single-stranded sequence knowledge, permitting a extra complete characterization of the biochemical properties not solely of historic DNA but in addition of cell-free DNA from human blood plasma, a clinically related marker for the analysis and monitoring of illness.
Description: Quantitativesandwich ELISA kit for measuring Human vascular endothelial cell growth factor E, VEGF-E in samples from serum, urine, cell culture supernates, tissue homogenates. A new trial version of the kit, which allows you to test the kit in your application at a reasonable price.
Human vascular endothelial cell growth factor E, VEGF-E ELISA Kit
Description: Quantitativesandwich ELISA kit for measuring Human vascular endothelial cell growth factor E, VEGF-E in samples from serum, urine, cell culture supernates, tissue homogenates. Now available in a cost efficient pack of 5 plates of 96 wells each, conveniently packed along with the other reagents in 5 separate kits.
