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AB264981

人USP42 knockout HeLa cell line

Human USP42 knockout HeLa cell line

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USP42 KO cell line available to order. KO validated. Free of charge wild type control available. Knockout achieved by using CRISPR/Cas9, 2 bp deletion in exon 2 and 5 bp deletion in exon 2 and 7 bp deletion in exon 2. To order both knockout and wild-type control cells: select '2 x 1000000 Cells/vial'. To order only knockout cells: select '1000000 Cells/vial'.

查看别名

Deubiquitinating enzyme 42, FLJ12697, UBP42_HUMAN, Ubiquitin carboxyl-terminal hydrolase 42, Ubiquitin thiolesterase 42, Ubiquitin-specific-processing protease 42, ubiquitin specific peptidase 42

3 Images
Sanger Sequencing - Human USP42 knockout HeLa cell line (AB264981)
  • Sanger seq

Unknown

Sanger Sequencing - Human USP42 knockout HeLa cell line (AB264981)

Allele-3 : 2 bp deletion in exon 2.

Sanger Sequencing - Human USP42 knockout HeLa cell line (AB264981)
  • Sanger seq

Unknown

Sanger Sequencing - Human USP42 knockout HeLa cell line (AB264981)

Allele-2 : 5 bp deletion in exon 2.

Sanger Sequencing - Human USP42 knockout HeLa cell line (AB264981)
  • Sanger seq

Unknown

Sanger Sequencing - Human USP42 knockout HeLa cell line (AB264981)

Allele-1 : 7 bp deletion in exon 2.

关键信息

细胞类型

HeLa

种属

Human

组织

Cervix

形式

Liquid

form

敲除验证

Sanger Sequencing

突变描述

Knockout achieved by using CRISPR/Cas9, 2 bp deletion in exon 2 and 5 bp deletion in exon 2 and 7 bp deletion in exon 2

疾病

Adenocarcinoma

产品详情

We will provide viable cells that proliferate on revival.

This product is subject to limited use licenses from The Broad Institute and ERS Genomics Limited, and is developed with patented technology. For full details of the limited use licenses and relevant patents please refer to our limited use license and patent pages.

规格

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性能和储存信息

基因名称
USP42
基因编辑类型
Knockout
基因编辑方法
CRISPR technology
敲除验证
Sanger Sequencing
运输条件
Dry Ice
推荐的短期储存条件
-196°C
推荐的长期储存条件
-196°C

处理步骤

初始处理指南

Upon arrival, the vial should be stored in liquid nitrogen vapor phase and not at -80°C. Storage at -80°C may result in loss of viability.

1. Thaw the vial in 37°C water bath for approximately 1-2 minutes.
2. Transfer the cell suspension (0.8 mL) to a 15 mL/50 mL conical sterile polypropylene centrifuge tube containing 8.4 mL pre-warmed culture medium, wash vial with an additional 0.8 mL culture medium (total volume 10 mL) to collect remaining cells, and centrifuge at 201 x g (rcf) for 5 minutes at room temperature. 10 mL represents minimum recommended dilution. 20 mL represents maximum recommended dilution.
3. Resuspend the cell pellet in 5 mL pre-warmed culture medium and count using a haemocytometer or alternative cell counting method seed all remaining cells into a T25.
4. Incubate the culture at 37°C incubator with 5% CO2. Check the culture one day after revival and continue to check until 80% confluent. Media change can be given if needed.
5. Once confluent passage into an appropriate flask at a density of 2x104 cells/cm2. Seeding density is given as a guide only and should be scaled to align with individual lab schedules. Cultures should be monitored daily.

传代培养指南
  • All seeding densities should be based on cell counts gained by established methods.
  • A guide seeding density of 2x104 cells/cm2 is recommended.
  • Cells should be passaged when they have achieved 80-90% confluence.
培养基

DMEM (High Glucose) + 10% FBS

低温储藏试剂

Cell Freezing Medium-DMSO Serum free media, contains 8.7% DMSO in MEM supplemented with methyl cellulose.

补充信息

This supplementary information is collated from multiple sources and compiled automatically.

USP42 also known as Ubiquitin-specific peptidase 42 is part of the ubiquitin-proteasome system. USP42 specifically removes ubiquitin molecules from specific protein substrates. This action involves deubiquitination a process that regulates protein degradation. The molecular weight of USP42 is approximately 150 kDa. In terms of expression USP42 is found in various tissues including the liver brain and kidneys indicating it has a broad role across different systems of the body.
Biological function summary

The function of USP42 is important in gene regulation and cell cycle control. By controlling protein stability it influences transcriptional activity and cellular responses to stress. USP42 associates with the p53 protein stabilizing it and enhancing its tumor suppressor function. Additionally it forms part of larger protein complexes that coordinate DNA damage responses. Through these interactions USP42 supports cellular health by ensuring proper repair and replication of DNA.

Pathways

In these pathways USP42 plays a part in modulating ubiquitin ligases and deubiquitinases activities maintaining protein homeostasis. The protein acts in concert with others like Mdm2 and p53 important for cellular stress responses and apoptosis. These pathways highlight the impact of USP42 in balancing cell survival and programmed cell death mechanisms.

Altered USP42 expression or function has links to tumorigenesis due to its interaction with proteins such as p53. Dysregulation in this pathway may contribute to cancer proliferation. In neurodegenerative conditions abnormal protein aggregation occurs if ubiquitin-proteasome function is impaired connecting to USP42's role in maintaining protein quality control. The protein's dysfunction can therefore influence disease progression by failing to regulate protein turnover properly.

质量控制

STR 分析

CSF1PO, D13S317, D7S820, D5S818, TH01, D16S539, TPOX

细胞培养

生物安全等级

EU: 2 US: 2

贴壁/悬浮

Adherent

性别

Female

产品实验方案

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