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AB265845

人USP34 knockout HeLa cell line

Human USP34 knockout HeLa cell line

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USP34 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 3 and 8 bp deletion in exon 3. 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 34, FLJ43910, KIAA0570, KIAA0729, MGC104459, UBP34_HUMAN, Ubiquitin carboxyl-terminal hydrolase 34, Ubiquitin specific protease 34, Ubiquitin thioesterase 34, Ubiquitin thiolesterase 34, Ubiquitin-specific-processing protease 34

2 Images
Sanger Sequencing - Human USP34 knockout HeLa cell line (AB265845)
  • Sanger seq

Unknown

Sanger Sequencing - Human USP34 knockout HeLa cell line (AB265845)

Allele-2 : 2 bp deletion in exon 3.

Sanger Sequencing - Human USP34 knockout HeLa cell line (AB265845)
  • Sanger seq

Unknown

Sanger Sequencing - Human USP34 knockout HeLa cell line (AB265845)

Allele-1 : 8 bp deletion in exon 3.

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 3 and 8 bp deletion in exon 3

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
USP34
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.

USP34 also known as ubiquitin specific peptidase 34 is a deubiquitinating enzyme that plays an essential role in the removal of ubiquitin moieties from target proteins. It weighs approximately 440 kDa. It is present in various tissues with notable expression in the brain heart and skeletal muscles. As a hydrolase USP34 removes ubiquitin chains affecting the stability and activity of proteins involved in several cellular processes.
Biological function summary

Ubiquitin specific peptidase 34 regulates protein homeostasis by controlling the degradation of ubiquitinated proteins. Its activity influences pathways such as Wnt signaling where it interacts with components of this signal transduction pathway to modulate cellular responses. Although USP34 can act independently it may also partner with other proteins in cellular complexes to assist in its deubiquitinating roles and to maintain appropriate protein levels.

Pathways

USP34 significantly impacts Wnt signaling and the TGF-beta pathway. In the Wnt signaling pathway it targets the degradation of beta-catenin which is pivotal for transcriptional activation in various cells. In the TGF-beta pathway USP34's regulation is important for promoting correct cellular responses. It interacts with proteins like SMAD and AXIN helping to maintain the pathways' integrity and balance cellular proliferation.

Ubiquitin specific peptidase 34 has connections to cancer and neurodegenerative diseases. Dysregulation of its deubiquitinating activity can result in abnormal protein stabilization which is a contributing factor in tumor growth and progression. In neurodegenerative diseases impaired USP34 function affects neuronal proteins linking it to disorders such as Alzheimer's disease. Proteins like beta-amyloid and tau often involved in these conditions have indirect associations with the activity of USP34 highlighting its potential role in disease processes.

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

Abcam Product Promise

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