首页 » NCI-H1568 [H1568]人源非小细胞肺癌细胞株Human Non-small cell lung cancer cells-BioVector NTCC Inc.

NCI-H1568 [H1568]人源非小细胞肺癌细胞株Human Non-small cell lung cancer cells-BioVector NTCC Inc.

  • 价  格:¥39850
  • 货  号:NTCC®-NCI-H1568 CRL-5876
  • 产  地:北京
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NCI-H1568 [H1568]人源非小细胞肺癌细胞株Human Non-small cell lung cancer cells-BioVector NTCC Inc.


NCI-H1568 [H1568] cells were isolated from the lungs of a 48-year-old, White female patient with non-small cell lung cancer: adenocarcinoma. This product has applications in cancer research.

Product category
Human cells
Organism
Homo sapiens, human
Tissue
Lung
Disease
Adenocarcinoma; Non-small cell lung cancer
Applications
3D cell culture
Cancer research
Product format
Frozen

Characteristics

Derivation
The line was established in December 1986 from lymph node metastasis of lung.
Age
48 years
Ethnicity
White
Gender
Female
Clinical data
The patient was a smoker. 60 pack years.
Metastatic
Lymph node

Handling information

Unpacking and storage instructions
  1. Check all containers for leakage or breakage.

  2. Remove the frozen cells from the dry ice packaging and immediately place the cells at a temperature below ­-130°C, preferably in liquid nitrogen vapor, until ready for use.

Complete medium
The base medium for this cell line is ATCC-formulated RPMI-1640 Medium, ATCC 30-2001. To make the complete growth medium, add the following components to the base medium: fetal bovine serum (ATCC 30-2020) to a final concentration of 10%.
Temperature
37°C
Handling procedure

To insure the highest level of viability, thaw the vial and initiate the culture as soon as possible upon receipt. If upon arrival, continued storage of the frozen culture is necessary, it should be stored in liquid nitrogen vapor phase and not at -70°C.  Storage at -70°C will result in loss of viability.

  1. Thaw the vial by gentle agitation in a 37°C water bath. To reduce the possibility of contamination, keep the O-ring and cap out of the water.  Thawing should be rapid (approximately 2 minutes).

  2. Remove the vial from the water bath as soon as the contents are thawed, and decontaminate by dipping in or spraying with 70% ethanol. All of the operations from this point on should be carried out under strict aseptic conditions.

  3. Transfer the vial contents to a 75 cm2 tissue culture flask and dilute with the recommended complete culture medium (see the specific batch information for the recommended dilution ratio).   It is important to avoid excessive alkalinity of the medium during recovery of the cells.  It is suggested that, prior to the addition of the vial contents, the culture vessel containing the growth medium be placed into the incubator for at least 15 minutes to allow the medium to reach its normal pH (7.0 to 7.6).

  4. Incubate the culture at 37°C in a suitable incubator.  A 5% CO2 in air atmosphere is recommended if using the medium described on this product sheet.

If it is desired that the cryoprotective agent be removed immediately, or that a more concentrated cell suspension be obtained, centrifuge the cell suspension at approximately 125 x g for 5 to 10 minutes.  Discard the supernatant and resuspend the cells with fresh growth medium at the dilution ratio recommended in the specific batch information.

Subculturing procedure
Remove medium, and rinse with 0.25% trypsin, 0.03% EDTA solution. Remove the solution and add an additional 1 to 2 mL of trypsin-EDTA solution. Allow the flask to sit at room temperature (or at 37°C) until the cells detach.Add fresh culture medium, aspirate and dispense into new culture flasks.
Subcultivation Ratio: A subcultivation ratio of 1:3 to 1:6 is recommended
Medium Renewal: Every 2 to 3 days
Reagents for cryopreservation
Complete growth medium supplemented with 5% (v/v) DMSO (ATCC 4-X)

Quality control specifications

Mycoplasma contamination
Not detected
STR profiling
Amelogenin: X
CSF1PO: 11
D13S317: 11
D16S539: 10,12
D5S818: 9
D7S820: 8,9
TH01: 9
TPOX: 8,11
vWA: 16,17
D3S1358: 17
D21S11: 29
D18S51
Penta_E: 12
Penta_D
D8S1179: 13,14
FGA
D19S433: 13,14
D2S1338: 18,20

History

Deposited as
Homo sapiens
Depositors
AF Gazdar, JD Minna
Year of origin
1986
Special collection
NCRR Contract

生产厂家Supplier:

BioVector NTCC质粒载体菌株细胞蛋白抗体基因保藏中心

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