Name細胞名稱：NTCC? GM25449 CHROMOSOME 16P12.1 DELETION SYNDROME B-Lymphocyte Cell Line
染色體 16P12.1 缺失綜合征細胞株
Description描述：Clinically affected; positive for 16p12.1 deletion; developmental delay; eating problems; gastrointestinal problems; sleep problems; self-injurious behaviors; bullying behavior; affected sister is GM25448; father is GM25452 and mother is GM25544; see extended family 3228.
Category分類：B-Lymphocyte
ID編號:NTCC?-GM25449
Size/Quantity數(shù)量: 1 Flask/2 Vials
Biosafety Level生物安全級別:1
Shipping Info運輸方式: RT/Dry Ice
Storage儲存方式: RT/Liquid Nitrogen
Race: White
Age年齡:2 YR
Gender性別:Male
Cell Type細胞類型: CHROMOSOME 16P12.1 DELETION SYNDROME
Affected State:Yes
Product:LCL
Gene:
Mutations突變:
Ethnicity:
Family:3228
Relationship:brother
Karyotype:46,XY.arr[hg19]16p12.2(21,807,854-22,431,358)x1_x000D_
Tissue Type組織來源:Blood
Complete Growth Medium完全培養(yǎng)基: BioVector? Roswell Park Memorial Institute Medium 1640 with 2mM L-glutamine or equivalent Complete Medium
Subculturing傳代方法:
Cryopreservation凍存方法:Freeze medium: Complete growth medium supplemented with 5% (v/v) DMSO
Storage temperature: liquid nitrogen vapor phase
Culture Conditions培養(yǎng)條件:Atmosphere: air, 95%; carbon dioxide (CO2), 5%
Temperature: 37.0°C
STR Profile鑒定數(shù)據(jù):
References參考文獻:

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