Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Calendula officinalis isolate:TN-82-766

ABSTRACT: Calendula officinalis isolate:TN-82-766 Genome sequencing and assembly

PROVIDER: PRJNA888267 | ENA |

REPOSITORIES: ENA

ACCESS DATA

Json Xml

Dataset's files

Source:

			Action	DRS
		Other

Items per page:

1 - 1 of 1

Similar Datasets

Calendula officinalis

Project description:Calendula officinalis

| PRJEB80524 | ENA

Calendula officinalis

Project description:Calendula officinalis overview

| PRJNA889157 | ENA

Calendula officinalis cultivar:Rajskij sad

Project description:Calendula officinalis cultivar:Rajskij sad Raw sequence reads

| PRJNA1021511 | ENA

The effect of oleanolic acid glucuronides from marigold (Calendula officinalis) on the possible modification of immunogenic proteins from infective Heigmosomoides polygyrus bakeri larvae (L3)

Project description:The aim of the present study was to determine the effects of glucuronides of oleanolic acid (GlcUAOA) extracted from Calendula officinalis flower on the profile of immunogenic proteins of somatic extract of infective H. polygyrus bakeri L3 stage.

2021-04-08 | PXD024205 | Pride

Regulus calendula

Project description:Regulus calendula

| PRJNA814974 | ENA

Calendula arvensis

Project description:Calendula arvensis

| PRJEB80545 | ENA

Genes altered by miR-766-5p in two cancer cell lines

Project description:To identify genes affected by miR-766-5p overexpression, we transfected with 10nmol of miR-766-5p or miR-negative control (NC) in HCT116-/-, or MIAPaCa2 cells. After 2 days, RNA was extracted, and then expression analysis was performed using agilent microarray.

2021-07-25 | GSE180688 | GEO

Regulus calendula

Project description:Regulus calendula (ruby-crowned kinglet), bRegCal1

| PRJNA1202539 | ENA

EXoO-Tn: Tag-n-Map the Tn Antigen in the Human Proteome

Project description:Tn antigen (Tn), a single N-acetylgalactosamine (GalNAc) monosaccharide attached to protein Ser and Thr residues, is found on most solid tumors yet rarely detected in adult tissues: featuring it one of the most distinctive signatures of cancers. Although it is prevalent in cancers, Tn-glycosylation sites are not entirely clear owing to the lack of suitable technology. Knowing the Tn-glycosylation sites will spur the development of the new vaccines, diagnostics, and therapeutics of cancers. Here, we report a novel technology named EXoO-Tn for large-scale mapping of Tn-glycosylation sites. EXoO-Tn utilizes glycosyltransferase C1GalT1 and isotopically-labeled UDP-Gal(13C6) to tag and convert Tn to Gal(13C6)-Tn. This exquisite Gal(13C6)-Tn structure is recognized by a human-gut-bacterial enzyme, called OpeRATOR, that specifically cleaves N-termini of the Gal(13C6)-Tn-occupied Ser and Thr residues to yield site-containing glycopeptides. The enzymes C1GalT1 and OpeRATOR could be used concurrently in one-pot. The effectiveness of EXoO-Tn was evaluated by analyzing Jurkat cells, where 947 Tn-glycosylation sites from 480 glycoproteins were mapped. Bioinformatic analysis of the identified site-specific Tn-glycoproteins revealed conserved motif, cellular localization, relative position in proteins, and mapped site-specific Tn-glycoproteome in different studies. Given the significance of Tn in cancers, EXoO-Tn is anticipated to have broad utilities in clinical study of cancers.

2022-02-15 | PXD014390 | Pride

Zea mays cultivar:RSQ-766

Project description:Zea mays RSQ-766 Transcriptome

| PRJNA493355 | ENA