-
E-mail
3004994300@qq.com
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Phone
13611928337,15021460884
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Address
No. 52 Chengliu Road, Jiading District, Shanghai
Shanghai Chuntest Biotechnology Co., Ltd
3004994300@qq.com
13611928337,15021460884
No. 52 Chengliu Road, Jiading District, Shanghai

After careful optimization by the team and long-term testing, this product can maintain good growth status of mouse primary oligodendrocytes.
This product already contains various ingredients required for the growth of mouse primary oligodendrocytes, and no additional ingredients are needed. It can be directly used for the cultivation of mouse primary oligodendrocytes.
Main components of the product
name |
volume |
concentration |
Storage conditions |
Primary oligodendrocyte basic culture medium |
500mL |
1× |
4 ℃, away from light |
Additive for primary oligodendrocyte culture |
5mL |
100× |
-20 ℃, away from light |
Fetal bovine serum(FBS) |
25mL |
final concentration5% |
-20 ℃, away from light |
Dual resistance (Penicillium)su/Streptomycinsu,P/S) |
5mL |
100× |
-20 ℃, away from light |
Transportation and storage
Transportation:Low temperature transportation in an insulated box containing biological ice packs
保存方法Store for 12 months according to the corresponding storage conditions, and store the prepared culture medium at 2 ℃ to 8 ℃ for 2 months;
quality control
Test Item |
quality control |
|
clarity |
clarify |
|
PH |
7.3±0.2 |
|
Endotoxin content (EU/mL) |
≤10 |
|
|
Sterility testing |
bacteria |
negative |
fungus |
negative |
|
Mycoplasma |
negative |
|
|
Cell growth assay |
cell morphology |
normal |
Cell Growth Experiment |
qualified |
|


Product Name |
|
Item Number |
EY-XP4291 |
Specifications |
100mL/500mL |
Technical Service |
Free technical support |
purpose |
For scientific research experiments only |


For scientific research purposes only.
Some components in the culture system are harmful to human health. Please do not use exposed skin to come into contact with the liquid in the culture system or containers containing residual liquid in the culture system; The concentration and harmfulness of these harmful substances are relatively low. If there is contact, rinse immediately with tap water.


The following experimental protocol introduces the general process of cell culture cryopreservation. A detailed experimental plan must refer to the product manual for specific cells.
1. Prepare frozen culture medium and store it at 2 ° C to 8 ° C until use. Please note that the type of cryopreservation medium used depends on the cell line used.
When freezing adherent cells, gently detach the cells from the tissue culture container using the method used during passage. Resuspend the cells in the required culture medium.
3. Use a hemocytometer or cell counter according to the trypan blue exclusion method or use Countess ® The automatic cell counter measures the total cell count and percentage of live cells. Calculate the required amount of frozen culture medium based on the required density of live cells.
4. Centrifuge the cell suspension at a centrifugal force of approximately 100-200 × g for 5 to 10 minutes. Carefully discard the supernatant under sterile conditions without stirring the cell sediment.
Note: The centrifugation speed and time depend on the type of cell.
5. Resuspend the cell pellet in pre cooled frozen culture medium and adjust it to the appropriate live cell density for the cell.
6. Divide the cell suspension into several cryovials. When packaging, cells should be gently mixed from time to time to maintain a uniform cell suspension state.
7. Use a freezing device with controllable cooling rate to freeze cells, reducing the temperature by approximately 1 ° C per minute. Alternatively, place the cryotube containing the cells into a cryobox and place the cryobox overnight at -80 ° C.

Human choriocarcinoma cells |
Specialized culture medium for primary human scleral fibroblasts |
Mouse leukemia clone cell line |
Mouse primary bone cell specific culture medium |
Human prostate cancer cells(Newly introduced in 2013 (preservation of stem cell bank) |
Specialized culture medium for primary oligodendrocytes in rats |
Human leukemiaT lymphocytes (preserved in stem cell bank) |
Specialized culture medium for rat primary scleral fibroblasts |
Human endometrial adenocarcinoma cells |
Specialized culture medium for rat primary thymic epithelial cells |
Human salivary gland adenoid cystic carcinoma cells |
Specialized culture medium for human primary corneal fibroblasts |
personT lymphocyte leukemia cells |
Specialized culture medium for primary rat placental trophoblast cells |
Human placental villous carcinoma cells |
Special medium for human primary pancreatic cancer cells |
Human acute lymphoblastic leukemia cells |
Specialized culture medium for human primary chondrocytes |
Mouse adrenal cortex tumor cells |
Specialized culture medium for mouse primary cerebral artery smooth muscle cells |
human gastric cancer cells KATO III (STR identification correct) |
Specialized culture medium for primary human osteoblasts |
Human thyroid squamous cell carcinoma cells |
Specialized culture medium for human primary umbilical artery outer membrane fibroblasts |
Human pharyngeal squamous cell carcinoma cells |
Specialized culture medium for rat primary adipose derived microvascular endothelial cells |
Human colorectal adenocarcinoma epithelial cells |
Mouse primary oligodendrocyte specific culture mediumSpecialized culture medium for human primary bone marrow mast cells |
Rat adrenal pheochromocytoma cells(Undifferentiated) |
Specialized culture medium for primary rat tendon stem cells |

The research object is living cells
During the experimental process, cell viability can be maintained as required, and the condition of some live cells can be monitored, detected, and even quantitatively evaluated for a long time, including their morphology, structure, and life activities.
2. Research conditions can be artificially controlled
pH、 The physical and chemical conditions such as temperature, oxygen, carbon dioxide, tension, etc. can be artificially controlled according to actual conditions. At the same time, chemical, physical, biological and other factors can be applied as conditions for experimental observation, and these factors can also be strictly controlled.
3. The research sample can achieve relatively uniformity
After a certain number of generations of cell culture, the obtained cell lines can achieve uniformity and belong to the same type of cells. If necessary, methods such as cloning can be used to purify the cells.
4. The research content is easy to observe, detect, and record
Various research techniques are used, such as inverted biomicroscopy, fluorescence microscopy, electron microscopy, flow cytometry, confocal laser microscopy, immunohistochemistry, in situ hybridization, isotope labeling, and other instruments and equipment. The recording methods can include photography, time-lapse movies, television, and other means.
5. The scope of the research is relatively broad
The applied disciplinary fields are relatively broad, such as cytology, immunology, oncology, biochemistry, genetics, molecular biology, etc;
The scope of applicability is wide, from lower animals to higher animals, and targeted research can be conducted on different age stages and tissues of an animal.
6. The cost of research is relatively economical
Can provide a large number of experimental subjects with similar biological characteristics, same period, good repeatability.