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Novogene cdna sequencing
Cdna Sequencing, supplied by Novogene, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/cdna+sequence/sequencing/pmc13156629-84-1-6
Average 86 stars, based on 1 article reviews
cdna sequencing - by Bioz Stars, 2026-10
86/100 stars

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other:

Article Title: Draft genome of Staphylococcus epidermidis clinical isolate OGSA-Sep-145 from an implant-related spinal infection.
Article Snippet: Libraries and sequencing were outsourced to Novogene (https://www.novogene.com/amea-en/) using the Next Generation Sequencing (NGS) DNA Library Prep Set kit (Cat No PT004) and Illumina NovaSeq X Plus Series (PE150) with 2 × 150 bp paired-end reads, achieving ~400× coverage.

Article Title: Effects of hypoxia on survival, apoptosis, and the transcriptome of the Chinese yellow pond turtle (Mauremys mutica).
Article Snippet: Mauremys mutica is a widely cultured pond turtle in China that can hold its breath underwater for up to 7 h. However, the adaptive mechanism of this hypoxia-resistant phenotype remains unknown.. In the present study, no M. mutica died until 6 h of hypoxic stress.. Inflammation was observed in the lungs of dead individuals along with a lung cell apoptosis rate of 12.3% in the death group, which was about six times that of the survival group.

Sequencing:

Article Title: Transcriptome sequencing reveals the regulatory mechanisms during the development of small white follicles to small yellow follicles in laying hens
Article Snippet: The products were purified with AMPure XP system (Beckman Coulter, Beverly, USA) and library quality was assessed using the Agilent Bioanalyzer 2100 system. .. The cDNA sequencing was performed at Novogene Bioinformatics Technology Co. (Beijing, China). ..

Article Title: Draft genome of Staphylococcus epidermidis clinical isolate OGSA-Sep-145 from an implant-related spinal infection
Article Snippet: Genomic DNA was extracted using the DNeasy PowerSoil Pro Kit (Qiagen, Milan, Italy). .. Libraries and sequencing were outsourced to Novogene ( https://www.novogene.com/amea-en/ ) using the Next Generation Sequencing (NGS) DNA Library Prep Set kit (Cat No PT004) and Illumina NovaSeq X Plus Series (PE150) with 2 × 150 bp paired-end reads, achieving ~400× coverage. .. The library was quantified using Qubit and quantitative Polymerase Chain Reaction (qPCR), and fragment sizes were assessed using an Agilent 5400 (Agilent, CA, US).

Article Title: E-cadherin endocytosis promotes non-canonical EGFR:STAT signalling to induce cell death and inhibit heterochromatinisation
Article Snippet: .. For each of the four genotypes ( UAS -myr::GFP, UAS -E-cad::EOS, UAS -STAT92E Y704F ::GFP and UAS - HP1 RNAi), three independent biological replicates were extracted. cDNA library sequencing was performed by Novogene, Cambridge, UK. ..

Article Title: Morphological Changes Induced by TKS4 Deficiency Can Be Reversed by EZH2 Inhibition in Colorectal Carcinoma Cells.
Article Snippet: The cell lysates were incubated overnight at 4 ◦C with the H3K27me3 monoclonal antibody (G.299.10), ChIP-verified (Life Technologies, Paisley, UK), and rabbit IgG (Sigma, St. Louis, MO, USA) negative control antibody provided by the kit. .. A total of 1 μg of DNA from each sample was sent for the construction of a cDNA library for Illumina high-throughput NGS sequencing (Novogene, Cambridge, UK). ..

Article Title: Identifying and validating potential therapeutic targets for septic heart failure and the cardioprotective effects of lycorine.
Article Snippet: Background: Septic heart failure has been recognized as a puzzle since antiquity and poses a major challenge to modern medicine.. Our previous work has demonstrated the potential effects of lycorine (LYC) on sepsis and septic myocardial injury.. Nonetheless, further exploration is needed to elucidate the underlying cellular and molecular mechanisms.

Next-Generation Sequencing:

Article Title: Draft genome of Staphylococcus epidermidis clinical isolate OGSA-Sep-145 from an implant-related spinal infection
Article Snippet: Genomic DNA was extracted using the DNeasy PowerSoil Pro Kit (Qiagen, Milan, Italy). .. Libraries and sequencing were outsourced to Novogene ( https://www.novogene.com/amea-en/ ) using the Next Generation Sequencing (NGS) DNA Library Prep Set kit (Cat No PT004) and Illumina NovaSeq X Plus Series (PE150) with 2 × 150 bp paired-end reads, achieving ~400× coverage. .. The library was quantified using Qubit and quantitative Polymerase Chain Reaction (qPCR), and fragment sizes were assessed using an Agilent 5400 (Agilent, CA, US).

Article Title: Morphological Changes Induced by TKS4 Deficiency Can Be Reversed by EZH2 Inhibition in Colorectal Carcinoma Cells.
Article Snippet: The cell lysates were incubated overnight at 4 ◦C with the H3K27me3 monoclonal antibody (G.299.10), ChIP-verified (Life Technologies, Paisley, UK), and rabbit IgG (Sigma, St. Louis, MO, USA) negative control antibody provided by the kit. .. A total of 1 μg of DNA from each sample was sent for the construction of a cDNA library for Illumina high-throughput NGS sequencing (Novogene, Cambridge, UK). ..

cDNA Library Assay:

Article Title: E-cadherin endocytosis promotes non-canonical EGFR:STAT signalling to induce cell death and inhibit heterochromatinisation
Article Snippet: .. For each of the four genotypes ( UAS -myr::GFP, UAS -E-cad::EOS, UAS -STAT92E Y704F ::GFP and UAS - HP1 RNAi), three independent biological replicates were extracted. cDNA library sequencing was performed by Novogene, Cambridge, UK. ..

Article Title: Morphological Changes Induced by TKS4 Deficiency Can Be Reversed by EZH2 Inhibition in Colorectal Carcinoma Cells.
Article Snippet: The cell lysates were incubated overnight at 4 ◦C with the H3K27me3 monoclonal antibody (G.299.10), ChIP-verified (Life Technologies, Paisley, UK), and rabbit IgG (Sigma, St. Louis, MO, USA) negative control antibody provided by the kit. .. A total of 1 μg of DNA from each sample was sent for the construction of a cDNA library for Illumina high-throughput NGS sequencing (Novogene, Cambridge, UK). ..

Construct:

Article Title: A GDSL esterase/lipase gene GbGELP identified from a fiber micronaire QTL qMIC-A11 modulates cell elongation and fiber development.
Article Snippet: Key message A fiber micronaire QTL qMIC-A11 was fine-mapped, and the GDSL esterase/lipase gene GbGELP was identified as the causal gene of the QTL.. GbGELP modulates cell elongation and cotton fiber development.. Abstract Fine mapping and map-based cloning of fiber micronaire (MIC)-related quantitative trait loci (QTL) have not been reported to date.

Genome DNA Library:

Article Title: A GDSL esterase/lipase gene GbGELP identified from a fiber micronaire QTL qMIC-A11 modulates cell elongation and fiber development.
Article Snippet: Key message A fiber micronaire QTL qMIC-A11 was fine-mapped, and the GDSL esterase/lipase gene GbGELP was identified as the causal gene of the QTL.. GbGELP modulates cell elongation and cotton fiber development.. Abstract Fine mapping and map-based cloning of fiber micronaire (MIC)-related quantitative trait loci (QTL) have not been reported to date.



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Image Search Results


Kaplan-Meier survival plots for A53T α-synuclein transgenic mice, A53T/Kcnn1-3copy mice, and A53T/Kcnn1-6copy mice. Median survival time was extended by 47% for the A53T/ Kcnn1-3copy mice and >100% for the A53T/Kcnn1-6copy mice. The two Kcnn1 transgenes are independent. See text for the different motor phenotypes of the A53T and A53T/Kcnn1-6copy mice.

Journal: bioRxiv

Article Title: Neuronal overexpression of mouse potassium channel subunit Kcnn1 in A53T α-synuclein mice more than doubles median survival time, associated with suppression of phospho-S129 α-synuclein formation

doi: 10.64898/2026.03.09.709927

Figure Lengend Snippet: Kaplan-Meier survival plots for A53T α-synuclein transgenic mice, A53T/Kcnn1-3copy mice, and A53T/Kcnn1-6copy mice. Median survival time was extended by 47% for the A53T/ Kcnn1-3copy mice and >100% for the A53T/Kcnn1-6copy mice. The two Kcnn1 transgenes are independent. See text for the different motor phenotypes of the A53T and A53T/Kcnn1-6copy mice.

Article Snippet: The mouse Kcnn1 cDNA sequence (NM_032397), was PCR-amplified from OriGene Technologies plasmid MR208601, omitting the 3’-terminal Myc-DDK tag sequence.

Techniques: Transgenic Assay

Absence of serine129 phospho-α-synuclein (Psynuclein) immunostaining in 12 mo A53T/Kcnn1-6copy mouse as compared with A53T endstage (9 mo) mouse. A. Location of superior colliculus (purple). Sagittal and coronal cross-sections of brain are shown, to illustrate midbrain dorsal position in the sagittal section and paired left and right structures in the coronal views. B. Sagittal views of superior colliculus, from 20 µm sagittal sections ∼1.2 mm from midline, showing presence of Kcnn1 overexpression in A53T/Kcnn1-6copy 12 month old mouse is associated with absence of α-synuclein disease-associated Psynuclein. Upper panels, A53T endstage 9 month old mouse sagitally sectioned and immunostained to reveal copious Psynuclein (left) and endogenous levels of Kcnn1 (right). Lower panels, absence of Psynuclein associated with overexpression of Kcnn1. Red arrow likely denotes intermediate gray layer. Scale bar, 200 μm.

Journal: bioRxiv

Article Title: Neuronal overexpression of mouse potassium channel subunit Kcnn1 in A53T α-synuclein mice more than doubles median survival time, associated with suppression of phospho-S129 α-synuclein formation

doi: 10.64898/2026.03.09.709927

Figure Lengend Snippet: Absence of serine129 phospho-α-synuclein (Psynuclein) immunostaining in 12 mo A53T/Kcnn1-6copy mouse as compared with A53T endstage (9 mo) mouse. A. Location of superior colliculus (purple). Sagittal and coronal cross-sections of brain are shown, to illustrate midbrain dorsal position in the sagittal section and paired left and right structures in the coronal views. B. Sagittal views of superior colliculus, from 20 µm sagittal sections ∼1.2 mm from midline, showing presence of Kcnn1 overexpression in A53T/Kcnn1-6copy 12 month old mouse is associated with absence of α-synuclein disease-associated Psynuclein. Upper panels, A53T endstage 9 month old mouse sagitally sectioned and immunostained to reveal copious Psynuclein (left) and endogenous levels of Kcnn1 (right). Lower panels, absence of Psynuclein associated with overexpression of Kcnn1. Red arrow likely denotes intermediate gray layer. Scale bar, 200 μm.

Article Snippet: The mouse Kcnn1 cDNA sequence (NM_032397), was PCR-amplified from OriGene Technologies plasmid MR208601, omitting the 3’-terminal Myc-DDK tag sequence.

Techniques: Immunostaining, Over Expression

Stereotactic injection of AAV9-CMV-Kcnn1 virus into the right superior colliculus of an asymptomatic 6 month old A53T mouse leads to overexpression of Kcnn1 in right superior colliculus (upper panel, outlined in light blue), associated with absence of Psynuclein (lower panel outlined in blue) observed after 54 days. Shown in upper and lower panels are separately immunostained neighboring 20 µm cryosections of flash-frozen brain. Upper panel, coronal section of brain showing right superior colliculus with clusters of fluorescent anti-Kcnn1-positive cells in what appear to be the bands of superficial, intermediate, and deep gray layers. Fluorescent cells are also observed beyond the boundaries of the superior colliculus, including crossing the midline and ventrally (see text). Lower panel, almost complete absence of Psynuclein staining in injected right superior colliculus region vs non-injected left (outlined and labeled in blue). (For detail on Psynuclein accumulation outside superior colliculus, see text). Scale bar 250 μm.

Journal: bioRxiv

Article Title: Neuronal overexpression of mouse potassium channel subunit Kcnn1 in A53T α-synuclein mice more than doubles median survival time, associated with suppression of phospho-S129 α-synuclein formation

doi: 10.64898/2026.03.09.709927

Figure Lengend Snippet: Stereotactic injection of AAV9-CMV-Kcnn1 virus into the right superior colliculus of an asymptomatic 6 month old A53T mouse leads to overexpression of Kcnn1 in right superior colliculus (upper panel, outlined in light blue), associated with absence of Psynuclein (lower panel outlined in blue) observed after 54 days. Shown in upper and lower panels are separately immunostained neighboring 20 µm cryosections of flash-frozen brain. Upper panel, coronal section of brain showing right superior colliculus with clusters of fluorescent anti-Kcnn1-positive cells in what appear to be the bands of superficial, intermediate, and deep gray layers. Fluorescent cells are also observed beyond the boundaries of the superior colliculus, including crossing the midline and ventrally (see text). Lower panel, almost complete absence of Psynuclein staining in injected right superior colliculus region vs non-injected left (outlined and labeled in blue). (For detail on Psynuclein accumulation outside superior colliculus, see text). Scale bar 250 μm.

Article Snippet: The mouse Kcnn1 cDNA sequence (NM_032397), was PCR-amplified from OriGene Technologies plasmid MR208601, omitting the 3’-terminal Myc-DDK tag sequence.

Techniques: Injection, Virus, Over Expression, Staining, Labeling

Absence of Psynuclein from right superior colliculus along ∼1 mm of rostro-caudal length of the AAV9-CMV-Kcnn1-injected mouse shown in (Mouse 1). The right and left superior colliculus are outlined in blue in all sections. Note that the shape of the outline is slightly altered from frame to frame to account for its position relative to surrounding landmarks (not shown) and compared with The Mouse Brain in Stereotaxic Coordinates, Franklin and Paxinos, 2007 . Coronal sections shown are spaced every 200 µm rostrocaudally. Consecutive 20 µm coronal sections of brain were taken, beginning at an arbitrary point several 100 µm rostral to superior colliculus and proceeding into the superior colliculus. Every 10 th section (sxn) was stained for Psynuclein. There is absence of Psynuclein from the injected right superior colliculus along the entire cut region. Section #89 appears to contain an artefact in its left aspect. Scale bar 250 μm. Figure 4B. A53T mouse injected with injection solution lacking virus (Control). Sections were collected and immunostained as in A. Superior colliculi circled in blue. There is symmetric presence of Psynuclein in the superior colliculi and outside of it. Scale bar 250 μm.

Journal: bioRxiv

Article Title: Neuronal overexpression of mouse potassium channel subunit Kcnn1 in A53T α-synuclein mice more than doubles median survival time, associated with suppression of phospho-S129 α-synuclein formation

doi: 10.64898/2026.03.09.709927

Figure Lengend Snippet: Absence of Psynuclein from right superior colliculus along ∼1 mm of rostro-caudal length of the AAV9-CMV-Kcnn1-injected mouse shown in (Mouse 1). The right and left superior colliculus are outlined in blue in all sections. Note that the shape of the outline is slightly altered from frame to frame to account for its position relative to surrounding landmarks (not shown) and compared with The Mouse Brain in Stereotaxic Coordinates, Franklin and Paxinos, 2007 . Coronal sections shown are spaced every 200 µm rostrocaudally. Consecutive 20 µm coronal sections of brain were taken, beginning at an arbitrary point several 100 µm rostral to superior colliculus and proceeding into the superior colliculus. Every 10 th section (sxn) was stained for Psynuclein. There is absence of Psynuclein from the injected right superior colliculus along the entire cut region. Section #89 appears to contain an artefact in its left aspect. Scale bar 250 μm. Figure 4B. A53T mouse injected with injection solution lacking virus (Control). Sections were collected and immunostained as in A. Superior colliculi circled in blue. There is symmetric presence of Psynuclein in the superior colliculi and outside of it. Scale bar 250 μm.

Article Snippet: The mouse Kcnn1 cDNA sequence (NM_032397), was PCR-amplified from OriGene Technologies plasmid MR208601, omitting the 3’-terminal Myc-DDK tag sequence.

Techniques: Injection, Staining, Virus, Control

Magnified views of corresponding regions of left and right superior colliculus from an AAV9 CMV-Kcnn1 virus-injected mouse at level of intermediate gray layers, immunostained with anti-Kcnn1 and anti-P-synuclein, showing near complete absence of Psynuclein in the presence of overexpressed Kcnn1. Displayed are 400 µm X 400 µm squares, taken from coronal section #60 (Kcnn1) and section #59 (Psynuclein) of Mouse 1, with their centers ∼1100 microns from either side of the midline. Anti-Kcnn1 (upper panels) shows brighter Kcnn1-immunoreactive cells on the virus-injected right side vs much less bright cells (endogenously expressing Kcnn1) on the uninjected left side. The number of Kcnn1-immunostained cells was roughly equal on the two sides (data not shown). Anti-Psynuclein (lower panels) shows copious intracellular Psynuclein on the left, in the setting of endogenous Kcnn1, and also that Psynuclein extends into processes and that a portion may be in glia or neuropil. On the right, in the setting of overexpressed Kcnn1, only four or five flecks of Psynuclein are visible, the rightmost of which appears to be intracellular. Scale bar 20 µm.

Journal: bioRxiv

Article Title: Neuronal overexpression of mouse potassium channel subunit Kcnn1 in A53T α-synuclein mice more than doubles median survival time, associated with suppression of phospho-S129 α-synuclein formation

doi: 10.64898/2026.03.09.709927

Figure Lengend Snippet: Magnified views of corresponding regions of left and right superior colliculus from an AAV9 CMV-Kcnn1 virus-injected mouse at level of intermediate gray layers, immunostained with anti-Kcnn1 and anti-P-synuclein, showing near complete absence of Psynuclein in the presence of overexpressed Kcnn1. Displayed are 400 µm X 400 µm squares, taken from coronal section #60 (Kcnn1) and section #59 (Psynuclein) of Mouse 1, with their centers ∼1100 microns from either side of the midline. Anti-Kcnn1 (upper panels) shows brighter Kcnn1-immunoreactive cells on the virus-injected right side vs much less bright cells (endogenously expressing Kcnn1) on the uninjected left side. The number of Kcnn1-immunostained cells was roughly equal on the two sides (data not shown). Anti-Psynuclein (lower panels) shows copious intracellular Psynuclein on the left, in the setting of endogenous Kcnn1, and also that Psynuclein extends into processes and that a portion may be in glia or neuropil. On the right, in the setting of overexpressed Kcnn1, only four or five flecks of Psynuclein are visible, the rightmost of which appears to be intracellular. Scale bar 20 µm.

Article Snippet: The mouse Kcnn1 cDNA sequence (NM_032397), was PCR-amplified from OriGene Technologies plasmid MR208601, omitting the 3’-terminal Myc-DDK tag sequence.

Techniques: Virus, Injection, Expressing