Lama-84 Cells
























General information
Description | LAMA-84 is a human cell line derived from the peripheral blood of a patient with chronic myeloid leukemia (CML) in blast crisis. This cell line is characterized by the presence of the Philadelphia chromosome, which results in the BCR-ABL fusion gene, a hallmark of CML. The BCR-ABL oncogene is known for its role in increasing tyrosine kinase activity, which promotes various signaling pathways leading to uncontrolled cell proliferation and resistance to apoptosis. LAMA-84 cells are thus an invaluable model for studying the molecular mechanisms of CML progression and for evaluating the efficacy of tyrosine kinase inhibitors (TKIs) in a pre-clinical setting. In research, LAMA-84 has been extensively used to understand the biology of CML, especially in the context of drug resistance and disease evolution. Studies involving this cell line have helped in elucidating the cellular responses to different generations of TKIs, such as imatinib, dasatinib, and nilotinib. Moreover, LAMA-84 has contributed to the investigation of new therapeutic strategies aimed at overcoming TKI resistance, including the testing of combination therapies that target other signaling pathways synergistically affected by the BCR-ABL fusion protein. |
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Organism | Human |
Tissue | Blood |
Disease | Chronic myeloid leukemia |
Synonyms | LAMA-84, LAMA84, Lama84 |
Characteristics
Age | 29 years |
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Gender | Female |
Ethnicity | Caucasian |
Morphology | Round cells |
Growth properties | Suspension, some adherent cells |
Identifiers / Biosafety / Citation
Citation | Lama-84 (Cytion catalog number 300261) |
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Biosafety level | 1 |
Expression / Mutation
Surface antigens | GPIIb/IIIa+, GPIIIa+ |
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Viruses | EBNA, EA, and VCA were not detected |
Mutational profile | BCR-ABL1 pos |
Handling
Culture Medium | Ham's F12, w: 1.0 mM stable Glutamine, w: 1.0 mM Sodium pyruvate, w: 1.1 g/L NaHCO3 (Cytion article number 820600a) |
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Medium supplements | Supplement the medium with 10% FBS |
Doubling time | 30 hours |
Subculturing | Cells adhering to the bottom of the cell culture flask may be dislodged by shaking. Maintain cultures by periodically adding or replacing the medium. Initiate cultures with a density of 2 x 10^5 cells/ml and keep the cell concentration within the range of 1 x 10^5 to 1 x 10^6 cells/ml for optimal growth. |
Split ratio | A ratio of 1:2 to 1:3 is recommended |
Seeding density | 1 to 2 x 10^4 cells/cm^2 |
Freezing recovery | After thawing, plate the cells at 5 x 10^4 cells/cm^2 and allow the cells to recover from the freezing process and to adhere for at least 24 hours. |
Freeze medium | As a cryopreservation medium, use complete growth medium (including FBS) + 10% DMSO for adequate post-thaw viability, or CM-1 (Cytion catalog number 800100), which includes optimized osmoprotectants and metabolic stabilizers to enhance recovery and reduce cryo-induced stress. |
Handling of cryopreserved cultures |
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Quality control / Genetic profile / HLA
Sterility | Mycoplasma contamination is excluded using both PCR-based assays and luminescence-based mycoplasma detection methods. To ensure there is no bacterial, fungal, or yeast contamination, cell cultures are subjected to daily visual inspections. |
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STR profile |
CSF1PO: 11,12,13
D13S317: 11
D16S539: 11
D5S818: 11,12
D7S820: 11
TH01: 6,7
TPOX: 10
vWA: 14,17
D3S1358: 14,17
D21S11: 29,30,31
D18S51: 13
Penta E: 7
Penta D: 10
D8S1179: 10,15
FGA: 21,22
D1S1656: 15,15.3
D6S1043: 10,20
D2S1338: 17
D12S391: 18,24
D19S433: 13
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HLA alleles |
A*: '02:01:01, '25:01:01
B*: '18:01:01, '44:02:01
C*: '05:01:01, '12:03:01
DRB1*: '04:02:01, '15:01:01G
DQA1*: '01:02:01, '03:01:01
DQB1*: '03:02:01, '06:02:01
DPB1*: '09:01:01, '23:01:01
E: '01:01:01
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Required products
One of its notable advantages is the ability to support cell growth without the need for serum supplementation. This eliminates potential interference caused by serum components, ensuring consistent and reliable experimental results. By providing a serum-free culture environment, Ham's F-12 Medium offers researchers greater control over their investigations.
Another key feature of Ham's F-12 Medium is its suitability for single-cell plating. This makes it an excellent choice for a variety of cell lines, including CHO cells, lung cells, and mouse L cells. The medium's optimized nutrient composition facilitates efficient attachment and growth of individual cells, enabling the establishment of homogeneous cell cultures with improved reproducibility.
Moreover, Ham's F-12 Medium has gained recognition as the preferred medium for the Clonal Toxicity Assay (CTA). This assay plays a critical role in assessing the cytotoxic effects of substances on cells. By utilizing Ham's F-12 Medium in the CTA, researchers can accurately evaluate the impact of various compounds or treatments on individual cells, providing valuable insights into toxicological profiles.
Quality control
pH = 7.2 +/
- 0.02 at 20-25°C.
Each lot has been tested for sterility and absence of mycoplasma and bacteria.
Maintenance
Keep refrigerated at +2°C to +8°C in the dark. Freezing and warming up to +37° C minimize the quality of the product.
Do not heat the medium to more than 37° C or use uncontrollable sources of heat (e.g., microwave appliances).
If only a part of the medium is to be used, remove this amount from the bottle and warm it up at room temperature.
Shelf life for any medium except for the basic medium is 8 weeks from the date of manufacture.
Composition
Components
mg/L
Inorganic Salts
Calcium chloride x 2H2O
44,00
Copper(II) sulfate x 5H2O
0,00
Iron (II) sulfate x 7H2O
0,83
Magnesium chloride x 6H2O
122,00
Potassium chloride
223,65
Sodium chloride
7599,00
di-Sodium hydrogen phosphateanhydrous
142,04
Zinc sulfate x 7H2O
0,86
Other Components
D(+)-Glucose anhydrous
1801,60
Hypoxanthine
4,08
Linoleic acid
0,08
DL-α-Lipoic acid
0,21
Phenol red
1,20
Putrescine x 2HCl
0,16
Sodium pyruvate
110,00
Thymidine
0,73
NaHCO3
1176,00
Amino Acids
L-Alanine
8,91
L-Arginine x HCl
210,70
L-Asparagine x H2O
15,01
L-Aspartic acid
13,31
L-Cysteine x HCl x H2O
35,12
L-Alanyl-L-Glutamine
217,30
L-Glutamic acid
14,71
Glycine
7,51
L-Histidine x HCl x H2O
20,96
L-Isoleucine
3,94
L-Leucine
13,12
L-Lysine x HCl
36,54
L-Methionine
4,48
L-Phenylalanine
4,96
L-Proline
34,53
L-Serine
10,51
L-Threonine
11,91
L-Tryptophan
2,04
L-Tyrosine
5,44
L-Valine
11,71
Vitamins
D(+)-Biotin
0,01
D-Calcium pantothenate
0,24
Choline chloride
13,96
Folic acid
1,32
myo-Inositol
18,02
Nicotinamide
0,04
Pyridoxine x HCl
0,06
Riboflavin
0,04
Thiamine x HCl
0,34
Vitamin B12
1,36
Phosphate-buffered saline (PBS) is a widely used buffer solution in biological and chemical research. It plays a crucial role in maintaining the pH balance and osmolarity during various experimental procedures, including tissue processing and cell culture. Our PBS solution is meticulously formulated with high-purity ingredients to ensure stability and reliability in every experiment. The osmolarity and ion concentrations of our PBS closely mimic those of the human body, making it isotonic and non-toxic to most cells.
Composition of Our PBS Solution
Our PBS solution is a pH-adjusted blend of ultrapure-grade phosphate buffers and saline solutions. At a 1X working concentration, it contains:
8000 mg/L Sodium chloride (NaCl)
200 mg/L Potassium chloride (KCl)
1150 mg/L Sodium phosphate dibasic anhydrous (Na2HPO4)
200 mg/L Potassium phosphate monobasic anhydrous (KH2PO4)
This composition ensures an optimal pH and ionic balance, suitable for a wide range of biological applications.
Applications of Our PBS Solution
Our PBS solution is ideal for various applications in biological research. Its isotonic and non-toxic properties make it suitable for substance dilution and cell container rinsing. PBS solutions containing EDTA are effective for disengaging attached and clumped cells. However, divalent metals such as zinc should not be added to PBS, as this can cause precipitation. In such cases, Good's buffers are recommended. Additionally, our PBS solution is an acceptable alternative to viral transport medium for the transport and storage of RNA viruses, including SARS-CoV-2.
Quality Control
Sterile-filtered
Storage and Shelf Life
Store at +2°C to +25°C, protected from light.
Once opened, store at 2°C to 25°C and use within 24 months.
Shipping Conditions
Ambient temperature
Maintenance
Keep refrigerated at +2°C to +8°C in the dark. Avoid freezing and frequent warming to +37°C, as it reduces product quality.
Do not heat the medium beyond 37°C or use uncontrolled heat sources such as microwave appliances.
If only part of the medium is to be used, remove the required amount and warm it to room temperature before use.
Composition
Category
Components
Concentration (mg/L)
Salts
Potassium chloride
200
Potassium phosphate monobasic anhydrous
200
Sodium chloride
8000
Sodium phosphate dibasic anhydrous
1150