ERS2647857
SAMEA4827976
Sample 1
10090
Mus musculus
Protocols: Stable GM6377 OR LOC108167440- and EGFP-expressing SP 2/0 cells, and the control EGFP-expressing SP 2/0 cells were collected after after cultured for 2 days in fresh medium. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. GM6377 OR LOC108167440 cDNA (General Biosystems, Anhui, China) was cloned into lentiviral vector EGFP-expressing LV201 (Fugene Corp., Guangzhou, China) to generate GM6377 OR LOC108167440 protein. Empty LV201 and GM6377 OR LOC108167440-expressing LV201 was transfected into SP 2/0 cells (ATCC® CRL-1581™, https://www.atcc.org/products/all/CRL-1581.aspx), and stable transfectants were identified by EGFP expression and drug selection (Puromycin, Sigma, 10 μg/ml). Stable GM6377 OR LOC108167440-expressing SP 2/0 cells and LV201-transduced SP 2/0 cells were cultured in fresh ATCC-formulated Dulbecco's Modified Eagle's Medium (Catalog No. 30-2002) containing 10% FBS, 2 mM glutamine, penicillin (100 IU/ml), streptomycin (100 g/ml), and 50 mM 2-mercaptoethanol. Cells were collected on ice after cultured for 2 days in fresh medium. Data were aligned using STAR with options --outFilterScoreMinOverLread 0.4 --outFilterMatchNminOverLread 0.4, against the C3H/HeJ genome as a reference (ftp://ftp.ensembl.org/pub/release-89/fasta/mus_musculus_c3hhej/dna/Mus_musculus_c3hhej.C3H_HeJ_v1.dna_sm.toplevel.fa.gz). Total RNA from cells was isolated and purified using the RNeasy Mini Kit (Qiagen, Venlo, Netherlands). All RNA content in the samples was measured with a NanoDrop®ND-1000 spectrophotometer, and the RNA quality was assessed using RNA 6000 NanoChips with the Agilent 2100 Bioanalyzer (Agilent, Palo Alto, CA, USA). Libraries were prepared using the TruSeq Stranded Total RNA Library Prep Kit with Ribo-Zero Gold (Illumina).
ENA-FIRST-PUBLIC
2020-08-13T04:04:16Z
ENA-LAST-UPDATE
2018-08-13T13:06:13Z
External Id
SAMEA4827976
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-08-13T04:04:16Z
INSDC last update
2018-08-13T13:06:13Z
INSDC status
public
Submitter Id
E-MTAB-7139:Sample 1
broker name
ArrayExpress
cell line
Sp2/0-Ag14
cell type
lymphocyte
common name
house mouse
disease
multiple myeloma
genotype
empty vector LV201
organism part
mixed spleen and skin
phenotype
empty vector
sample name
E-MTAB-7139:Sample 1
scientific_name
Mus musculus
ERS2647858
SAMEA4827977
Sample 2
10090
Mus musculus
Protocols: Stable GM6377 OR LOC108167440- and EGFP-expressing SP 2/0 cells, and the control EGFP-expressing SP 2/0 cells were collected after after cultured for 2 days in fresh medium. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. GM6377 OR LOC108167440 cDNA (General Biosystems, Anhui, China) was cloned into lentiviral vector EGFP-expressing LV201 (Fugene Corp., Guangzhou, China) to generate GM6377 OR LOC108167440 protein. Empty LV201 and GM6377 OR LOC108167440-expressing LV201 was transfected into SP 2/0 cells (ATCC® CRL-1581™, https://www.atcc.org/products/all/CRL-1581.aspx), and stable transfectants were identified by EGFP expression and drug selection (Puromycin, Sigma, 10 μg/ml). Stable GM6377 OR LOC108167440-expressing SP 2/0 cells and LV201-transduced SP 2/0 cells were cultured in fresh ATCC-formulated Dulbecco's Modified Eagle's Medium (Catalog No. 30-2002) containing 10% FBS, 2 mM glutamine, penicillin (100 IU/ml), streptomycin (100 g/ml), and 50 mM 2-mercaptoethanol. Cells were collected on ice after cultured for 2 days in fresh medium. Data were aligned using STAR with options --outFilterScoreMinOverLread 0.4 --outFilterMatchNminOverLread 0.4, against the C3H/HeJ genome as a reference (ftp://ftp.ensembl.org/pub/release-89/fasta/mus_musculus_c3hhej/dna/Mus_musculus_c3hhej.C3H_HeJ_v1.dna_sm.toplevel.fa.gz). Total RNA from cells was isolated and purified using the RNeasy Mini Kit (Qiagen, Venlo, Netherlands). All RNA content in the samples was measured with a NanoDrop®ND-1000 spectrophotometer, and the RNA quality was assessed using RNA 6000 NanoChips with the Agilent 2100 Bioanalyzer (Agilent, Palo Alto, CA, USA). Libraries were prepared using the TruSeq Stranded Total RNA Library Prep Kit with Ribo-Zero Gold (Illumina).
ENA-FIRST-PUBLIC
2020-08-13T04:04:16Z
ENA-LAST-UPDATE
2018-08-13T13:06:13Z
External Id
SAMEA4827977
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-08-13T04:04:16Z
INSDC last update
2018-08-13T13:06:13Z
INSDC status
public
Submitter Id
E-MTAB-7139:Sample 2
broker name
ArrayExpress
cell line
Sp2/0-Ag14
cell type
lymphocyte
common name
house mouse
disease
multiple myeloma
genotype
LV201_Gm6377
organism part
mixed spleen and skin
phenotype
Gm6377 overexpression
sample name
E-MTAB-7139:Sample 2
scientific_name
Mus musculus
ERS2647859
SAMEA4827978
Sample 3
10090
Mus musculus
Protocols: Stable GM6377 OR LOC108167440- and EGFP-expressing SP 2/0 cells, and the control EGFP-expressing SP 2/0 cells were collected after after cultured for 2 days in fresh medium. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. GM6377 OR LOC108167440 cDNA (General Biosystems, Anhui, China) was cloned into lentiviral vector EGFP-expressing LV201 (Fugene Corp., Guangzhou, China) to generate GM6377 OR LOC108167440 protein. Empty LV201 and GM6377 OR LOC108167440-expressing LV201 was transfected into SP 2/0 cells (ATCC® CRL-1581™, https://www.atcc.org/products/all/CRL-1581.aspx), and stable transfectants were identified by EGFP expression and drug selection (Puromycin, Sigma, 10 μg/ml). Stable GM6377 OR LOC108167440-expressing SP 2/0 cells and LV201-transduced SP 2/0 cells were cultured in fresh ATCC-formulated Dulbecco's Modified Eagle's Medium (Catalog No. 30-2002) containing 10% FBS, 2 mM glutamine, penicillin (100 IU/ml), streptomycin (100 g/ml), and 50 mM 2-mercaptoethanol. Cells were collected on ice after cultured for 2 days in fresh medium. Data were aligned using STAR with options --outFilterScoreMinOverLread 0.4 --outFilterMatchNminOverLread 0.4, against the C3H/HeJ genome as a reference (ftp://ftp.ensembl.org/pub/release-89/fasta/mus_musculus_c3hhej/dna/Mus_musculus_c3hhej.C3H_HeJ_v1.dna_sm.toplevel.fa.gz). Total RNA from cells was isolated and purified using the RNeasy Mini Kit (Qiagen, Venlo, Netherlands). All RNA content in the samples was measured with a NanoDrop®ND-1000 spectrophotometer, and the RNA quality was assessed using RNA 6000 NanoChips with the Agilent 2100 Bioanalyzer (Agilent, Palo Alto, CA, USA). Libraries were prepared using the TruSeq Stranded Total RNA Library Prep Kit with Ribo-Zero Gold (Illumina).
ENA-FIRST-PUBLIC
2020-08-13T04:04:16Z
ENA-LAST-UPDATE
2018-08-13T13:06:13Z
External Id
SAMEA4827978
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-08-13T04:04:16Z
INSDC last update
2018-08-13T13:06:13Z
INSDC status
public
Submitter Id
E-MTAB-7139:Sample 3
broker name
ArrayExpress
cell line
Sp2/0-Ag14
cell type
lymphocyte
common name
house mouse
disease
multiple myeloma
genotype
LV201_Loc108167440
organism part
mixed spleen and skin
phenotype
Loc108167440 overexpression
sample name
E-MTAB-7139:Sample 3
scientific_name
Mus musculus