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Shanghai Chuntest Biotechnology Co., Ltd

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    3004994300@qq.com

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    13611928337,15021460884

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Mouse primary oligodendrocyte specific culture medium

NegotiableUpdate on 04/24
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Overview
The company is selling products specifically designed for mouse primary oligodendrocyte culture medium: rat primary tendon stem cell culture medium, human primary rectal fibroblast culture medium, human primary melanocyte culture medium, mouse primary uterine microvascular endothelial cell culture medium, human primary thyroid microvascular endothelial cell culture medium, rat primary T lymphocyte culture medium, human primary dental pulp stem cell culture medium, human primary ovarian stromal cell culture medium, rat primary renal cell culture medium, rabbit primary periodontal ligament fibroblast culture medium
Product Details

小鼠原代少突胶质细胞专用培养基

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

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/StreptomycinsuP/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



小鼠原代少突胶质细胞专用培养基

小鼠原代少突胶质细胞专用培养基

Product Name

Mouse primary oligodendrocyte specific culture medium

Item Number

EY-XP4291

Specifications

100mL/500mL

Technical Service

Free technical support

purpose

For scientific research experiments only


小鼠原代少突胶质细胞专用培养基


小鼠原代少突胶质细胞专用培养基

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.

小鼠原代少突胶质细胞专用培养基

小鼠原代少突胶质细胞专用培养基

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.

小鼠原代少突胶质细胞专用培养基

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


小鼠原代少突胶质细胞专用培养基

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.