ERS3737782
SAMEA5949295
Sample 6
10090
Mus musculus
Protocols: Splenic lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. Mice were euthanized using CO2. Spleens and Lymph nodes (LNs) were cut using scissors. B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice were developed by Cyagen Co., Ltd (Guangzhou, China). Splenic and lymph nodes (LNs) lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. 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 was extracted from 107 PBMCs using TRIzol reagent (Life Technologies).Total RNA from cells was 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
2020-07-31T04:03:47Z
ENA-LAST-UPDATE
2019-09-11T12:13:03Z
External Id
SAMEA5949295
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-07-31T04:03:47Z
INSDC last update
2019-09-11T12:13:03Z
INSDC status
public
Submitter Id
E-MTAB-8320:Sample 6
age
9
broker name
ArrayExpress
cell type
B cell
common name
house mouse
developmental stage
adult
genotype
Gm40600 Tg
organism part
spleen
sample name
E-MTAB-8320:Sample 6
scientific_name
Mus musculus
sex
female
strain
C57BL/6
ERS3737783
SAMEA5949296
Sample 8
10090
Mus musculus
Protocols: Splenic lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. Mice were euthanized using CO2. Spleens and Lymph nodes (LNs) were cut using scissors. B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice were developed by Cyagen Co., Ltd (Guangzhou, China). Splenic and lymph nodes (LNs) lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. 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 was extracted from 107 PBMCs using TRIzol reagent (Life Technologies).Total RNA from cells was 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
2020-07-31T04:03:47Z
ENA-LAST-UPDATE
2019-09-11T12:13:12Z
External Id
SAMEA5949296
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-07-31T04:03:47Z
INSDC last update
2019-09-11T12:13:12Z
INSDC status
public
Submitter Id
E-MTAB-8320:Sample 8
age
9
broker name
ArrayExpress
cell type
B cell
common name
house mouse
developmental stage
adult
genotype
Gm40600 Tg
organism part
lymph node
sample name
E-MTAB-8320:Sample 8
scientific_name
Mus musculus
sex
female
strain
C57BL/6
ERS3737784
SAMEA5949297
Sample 5
10090
Mus musculus
Protocols: Splenic lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. Mice were euthanized using CO2. Spleens and Lymph nodes (LNs) were cut using scissors. B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice were developed by Cyagen Co., Ltd (Guangzhou, China). Splenic and lymph nodes (LNs) lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. 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 was extracted from 107 PBMCs using TRIzol reagent (Life Technologies).Total RNA from cells was 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
2020-07-31T04:03:47Z
ENA-LAST-UPDATE
2019-09-11T12:13:17Z
External Id
SAMEA5949297
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-07-31T04:03:47Z
INSDC last update
2019-09-11T12:13:17Z
INSDC status
public
Submitter Id
E-MTAB-8320:Sample 5
age
9
broker name
ArrayExpress
cell type
B cell
common name
house mouse
developmental stage
adult
genotype
wild type genotype
organism part
spleen
sample name
E-MTAB-8320:Sample 5
scientific_name
Mus musculus
sex
female
strain
C57BL/6
ERS3737785
SAMEA5949298
Sample 7
10090
Mus musculus
Protocols: Splenic lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. Mice were euthanized using CO2. Spleens and Lymph nodes (LNs) were cut using scissors. B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice were developed by Cyagen Co., Ltd (Guangzhou, China). Splenic and lymph nodes (LNs) lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. 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 was extracted from 107 PBMCs using TRIzol reagent (Life Technologies).Total RNA from cells was 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
2020-07-31T04:03:47Z
ENA-LAST-UPDATE
2019-09-11T12:13:22Z
External Id
SAMEA5949298
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-07-31T04:03:47Z
INSDC last update
2019-09-11T12:13:22Z
INSDC status
public
Submitter Id
E-MTAB-8320:Sample 7
age
9
broker name
ArrayExpress
cell type
B cell
common name
house mouse
developmental stage
adult
genotype
wild type genotype
organism part
lymph node
sample name
E-MTAB-8320:Sample 7
scientific_name
Mus musculus
sex
female
strain
C57BL/6
ERS3737786
SAMEA5949299
Sample 2
10090
Mus musculus
Protocols: Splenic lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. Mice were euthanized using CO2. Spleens and Lymph nodes (LNs) were cut using scissors. B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice were developed by Cyagen Co., Ltd (Guangzhou, China). Splenic and lymph nodes (LNs) lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. 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 was extracted from 107 PBMCs using TRIzol reagent (Life Technologies).Total RNA from cells was 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
2020-07-31T04:03:47Z
ENA-LAST-UPDATE
2019-09-11T12:13:31Z
External Id
SAMEA5949299
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-07-31T04:03:47Z
INSDC last update
2019-09-11T12:13:31Z
INSDC status
public
Submitter Id
E-MTAB-8320:Sample 2
age
9
broker name
ArrayExpress
cell type
B cell
common name
house mouse
developmental stage
adult
genotype
Gm40600 Tg
organism part
spleen
sample name
E-MTAB-8320:Sample 2
scientific_name
Mus musculus
sex
female
strain
C57BL/6
ERS3737787
SAMEA5949300
Sample 4
10090
Mus musculus
Protocols: Splenic lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. Mice were euthanized using CO2. Spleens and Lymph nodes (LNs) were cut using scissors. B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice were developed by Cyagen Co., Ltd (Guangzhou, China). Splenic and lymph nodes (LNs) lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. 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 was extracted from 107 PBMCs using TRIzol reagent (Life Technologies).Total RNA from cells was 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
2020-07-31T04:03:47Z
ENA-LAST-UPDATE
2019-09-11T12:13:42Z
External Id
SAMEA5949300
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-07-31T04:03:47Z
INSDC last update
2019-09-11T12:13:42Z
INSDC status
public
Submitter Id
E-MTAB-8320:Sample 4
age
9
broker name
ArrayExpress
cell type
B cell
common name
house mouse
developmental stage
adult
genotype
Gm40600 Tg
organism part
lymph node
sample name
E-MTAB-8320:Sample 4
scientific_name
Mus musculus
sex
female
strain
C57BL/6
ERS3737788
SAMEA5949301
Sample 1
10090
Mus musculus
Protocols: Splenic lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. Mice were euthanized using CO2. Spleens and Lymph nodes (LNs) were cut using scissors. B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice were developed by Cyagen Co., Ltd (Guangzhou, China). Splenic and lymph nodes (LNs) lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. 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 was extracted from 107 PBMCs using TRIzol reagent (Life Technologies).Total RNA from cells was 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
2020-07-31T04:03:47Z
ENA-LAST-UPDATE
2019-09-11T12:13:53Z
External Id
SAMEA5949301
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-07-31T04:03:47Z
INSDC last update
2019-09-11T12:13:53Z
INSDC status
public
Submitter Id
E-MTAB-8320:Sample 1
age
9
broker name
ArrayExpress
cell type
B cell
common name
house mouse
developmental stage
adult
genotype
wild type genotype
organism part
spleen
sample name
E-MTAB-8320:Sample 1
scientific_name
Mus musculus
sex
female
strain
C57BL/6
ERS3737789
SAMEA5949302
Sample 3
10090
Mus musculus
Protocols: Splenic lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. Mice were euthanized using CO2. Spleens and Lymph nodes (LNs) were cut using scissors. B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice were developed by Cyagen Co., Ltd (Guangzhou, China). Splenic and lymph nodes (LNs) lymphocytes were isolated from 9-week-old female wildtype (WT) mice and Gm40600 transgenic (Gm40600 Tg) mice (3 mice/group) using Ficoll (Ficoll-Paque Plus, GE Healthcre). B cells were sorted by B220 microbeads (Cat No. 130-049-501, Miltenyi Biotec, Germany) or stimulated for 3 days with 10 ug/ml LPS. Samples were washed twice with PBS and 1 mL of TRIzol per 1 x 107 cell pellets was added and frozen in -80℃. 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 was extracted from 107 PBMCs using TRIzol reagent (Life Technologies).Total RNA from cells was 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
2020-07-31T04:03:47Z
ENA-LAST-UPDATE
2019-09-11T12:13:59Z
External Id
SAMEA5949302
INSDC center name
Beijing Institute of Basic Medical Sciences
INSDC first public
2020-07-31T04:03:47Z
INSDC last update
2019-09-11T12:13:59Z
INSDC status
public
Submitter Id
E-MTAB-8320:Sample 3
age
9
broker name
ArrayExpress
cell type
B cell
common name
house mouse
developmental stage
adult
genotype
wild type genotype
organism part
lymph node
sample name
E-MTAB-8320:Sample 3
scientific_name
Mus musculus
sex
female
strain
C57BL/6