RAB32 Knockout iBMDM Cell Line

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LM02108019832

Product ID： LM02108019832

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产品描述
细胞复苏
细胞传代
细胞冻存
抗体验证结果

- Commodity name: RAB32 Knockout iBMDM Cell Line
- Commodity ID: LM02108019832
- Gene Symbol: Rab32
- Ensembl ID: ENSMUSG00000019832
- Uniprot ID: Q9CZE3
- 宿主细胞 / 类型: IBMDM/immortalized mouse bone marrow macrophages
- NCBI Gene ID: 67844
- 规格: 1×10^6 cells/ cryovials
- 生长培养基: Dedicated culture medium
- 筛选标记: N/A
- 生长特性: Adherent cells, irregular morphology
- 培养条件: 37℃, 5% CO2 incubator, passage 1/2 to 1/4
- 倍增时间: ~24-48 hours
- 参考换液频率: 2-3 times/week
- 支原体检测结果: Negative
- 敲除效率（Sanger测序）: 100%
- 蛋白质组验证结果: Mass spectrometry verification passed
- 抗体货号: Adding
- 目标基因介绍: Acts as an A-kinase anchoring protein by binding to the type II regulatory subunit of protein kinase A and anchoring it to the mitochondrion. Also involved in synchronization of mitochondrial fission. Plays a role in the maturation of phagosomes that engulf pathogens, such as S.aureus and Mycobacterium (By similarity). Plays an important role in the control of melanin production and melanosome biogenesis (By similarity). In concert with RAB38, regulates the proper trafficking of melanogenic enzymes TYR, TYRP1 and DCT/TYRP2 to melanosomes in melanocytes (PubMed:26620560). Stimulates phosphorylation of RAB10 Thr-73 by LRRK2 (By similarity).
- 细胞开发路径: A stable KO cell pool was generated using the CRISPR-RNP method; Sanger sequencing results showed 100% knockout efficiency in the KO cell pool
- 应用: Highly efficient gene knockout cell lines (KO Cell Line) are particularly suitable for preliminary functional analysis, the development of complex disease models, precision drug screening, and a wide range of gene discovery research.
Key words:
- Rab32
01. Preheat the complete medium in a 37℃ water bath.
02. Thaw the frozen tube in a 37℃ water bath for 1-2 minutes.
03. Transfer the frozen tube to a biosafety cabinet and wipe the surface with 70% ethanol.
04. Unscrew the cap of the frozen tube and gently transfer the cell suspension to a sterile centrifuge tube containing 9mL of complete medium.
05. Centrifuge at 125g for 5-7 minutes at room temperature, discard the supernatant.
06. Resuspend the cell pellet with 5mL of complete medium and transfer the cell suspension to a T25 culture flask.
07. Transfer the cells to an incubator at 37℃, 5% CO2.
08. Reference passage ratio: 1/2 to 1/4 passage, full growth in 2-3 days.
01. When the cell confluence in the culture flask reaches over 80%-90%, the cells can be passaged.
02. Take out the culture medium, PBS, trypsin (0.25% Trypsin_EDTA Gibco 25200-056), etc. from the 4℃ refrigerator, place them in a 37℃ water bath until the temperature is close to 37℃, take them out, spray 75% alcohol on the surface of the bottle, and place them in a biosafety cabinet.

03. Take out the culture flask to be passaged from the incubator, spray the bottle with 75% alcohol, and place it in a biosafety cabinet.
04. To avoid dispersing the cells, rinse the cells with PBS along the upper wall of the culture flask, discard after washing the cells, add 2mL to T25.
05. Add the corresponding volume of trypsin (1.5mL for T75, 0.5mL for T25), and gently shake the bottle to spread the trypsin evenly over the bottom of the cells. The dosage can be increased or decreased appropriately depending on the actual situation. When most of the cells fall off after about 1-2min, add the corresponding volume of complete culture medium to stop digestion, and gently pipet with a 5mL pipette until all the cells fall off.
06. Transfer the cell suspension to a 15mL centrifuge tube, centrifuge the suspension at 300g for 5min, and discard the supernatant.
07. Transfer 5mL of complete culture medium to resuspend the cells, adjust the inoculation ratio as needed, and supplement the complete culture medium in the culture flask, add to 13-15mL for T75, add to 5mL for T25, and add 1% double antibody.
08. After covering the bottle cap and tightening it, gently shake the bottle to mix the cells evenly, and then place it in a 37℃, 5% CO2 incubator.
01. Prepare the freezing solution and pre-chill it in advance.
02. Ensure that the cells to be frozen meet the freezing requirements. Check the following conditions under a microscope: healthy appearance and morphological characteristics, growth cycle (late logarithmic phase), no signs of contamination or degradation.
03. Digest and centrifuge the cells (refer to the subculture procedure for specific steps).
04. Resuspend the cells with freezing solution at a volume of 1mL per tube, mix well, and aliquot into cryopreservation tubes.
05. Place the cells in a controlled-rate freezing container and freeze in a -80℃ freezer.
06. Subsequently, transfer the cells to a liquid nitrogen tank for long-term storage.
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