Hs 67

规格:

货期:

编号:TS211913

品牌:Testobio

产品名称：	Hs 67
商品货号：	TS211913
Organism：	Homo sapiens, human
Tissue：	thymus
Product Format：	frozen
Morphology：	fibroblast
Culture Properties：	adherent
Biosafety Level：	1 Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Disease：	normal
Age：	newborn
Gender：	male
Ethnicity：	Caucasian
Karyotype：	diploid
Derivation：	Hs 67 was developed in 1969 at the Naval Biosciences Laboratory by R. Owens from the thymus of a 6 pound, apparently normal, male.
Clinical Data：	Hs 67 was developed in 1969 at the Naval Biosciences Laboratory by R. Owens from the thymus of a 6 pound, apparently normal, male. male Caucasian newborn
Comments：	This line was also previously distributed by ATCC as CRL-7828 (Hs 67.Th). Hs 67 was developed in 1969 at the Naval Biosciences Laboratory by R. Owens from the thymus of a 6 pound, apparently normal, male.
Complete Growth Medium：	The base medium for this cell line is ATCC-formulated Dulbeccos Modified Eagles Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing：	Protocol: Remove and discard culture medium. Briefly rinse the cell layer with Hanks Balanced Salt Solution or 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor. Add 1.0 to 2.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes). Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting Add appropriate aliquots of the cell suspension to new culture vessels. Incubate cultures at 37°C. Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended Medium Renewal: 2 to 3 times per week
Cryopreservation：	Culture medium, 95%; DMSO, 5%
Culture Conditions：	Atmosphere: air, 95%; carbon dioxide (CO2), 5%
STR Profile：	Amelogenin: X CSF1PO: 11,12 D13S317: 11,12 D16S539: 11,13 D5S818: 12 D7S820: 8,12 THO1: 6,9.3 TPOX: 8,12 vWA: 16,17
Isoenzymes：	AK-1, 1 ES-D, 1 G6PD, B GLO-I, 1-2 Me-2, 1 PGM1, 1 PGM3, 1
Name of Depositor：	RB Owens
Deposited As：	Homo sapiens

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Hs 67

货号: TS211913
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产品名称：	Hs 67
商品货号：	TS211913
Organism：	Homo sapiens, human
Tissue：	thymus
Product Format：	frozen
Morphology：	fibroblast
Culture Properties：	adherent
Biosafety Level：	1 Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Disease：	normal
Age：	newborn
Gender：	male
Ethnicity：	Caucasian
Karyotype：	diploid
Derivation：	Hs 67 was developed in 1969 at the Naval Biosciences Laboratory by R. Owens from the thymus of a 6 pound, apparently normal, male.
Clinical Data：	Hs 67 was developed in 1969 at the Naval Biosciences Laboratory by R. Owens from the thymus of a 6 pound, apparently normal, male. male Caucasian newborn
Comments：	This line was also previously distributed by ATCC as CRL-7828 (Hs 67.Th). Hs 67 was developed in 1969 at the Naval Biosciences Laboratory by R. Owens from the thymus of a 6 pound, apparently normal, male.
Complete Growth Medium：	The base medium for this cell line is ATCC-formulated Dulbeccos Modified Eagles Medium, Catalog No. 30-2002. To make the complete growth medium, add the following components to the base medium: fetal bovine serum to a final concentration of 10%.
Subculturing：	Protocol: Remove and discard culture medium. Briefly rinse the cell layer with Hanks Balanced Salt Solution or 0.25% (w/v) Trypsin- 0.53 mM EDTA solution to remove all traces of serum that contains trypsin inhibitor. Add 1.0 to 2.0 ml of Trypsin-EDTA solution to flask and observe cells under an inverted microscope until cell layer is dispersed (usually within 5 to 15 minutes). Note: To avoid clumping do not agitate the cells by hitting or shaking the flask while waiting for the cells to detach. Cells that are difficult to detach may be placed at 37°C to facilitate dispersal. Add 6.0 to 8.0 ml of complete growth medium and aspirate cells by gently pipetting Add appropriate aliquots of the cell suspension to new culture vessels. Incubate cultures at 37°C. Subcultivation Ratio: A subcultivation ratio of 1:2 to 1:4 is recommended Medium Renewal: 2 to 3 times per week
Cryopreservation：	Culture medium, 95%; DMSO, 5%
Culture Conditions：	Atmosphere: air, 95%; carbon dioxide (CO2), 5%
STR Profile：	Amelogenin: X CSF1PO: 11,12 D13S317: 11,12 D16S539: 11,13 D5S818: 12 D7S820: 8,12 THO1: 6,9.3 TPOX: 8,12 vWA: 16,17
Isoenzymes：	AK-1, 1 ES-D, 1 G6PD, B GLO-I, 1-2 Me-2, 1 PGM1, 1 PGM3, 1
Name of Depositor：	RB Owens
Deposited As：	Homo sapiens