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AB263191

Human ERMP1 knockout HeLa cell lysate

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ERMP1 KO cell lysate available now. KO validated. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, Homozygous: 1 bp insertion in exon 1.
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Sanger Sequencing - Human ERMP1 knockout HeLa cell lysate (AB263191)
  • Sanger seq

Unknown

Sanger Sequencing - Human ERMP1 knockout HeLa cell lysate (AB263191)

Homozygous : 1 bp insertion in exon 1

Key facts

Cell type

HeLa

Species or organism

Human

Tissue

Cervix

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, Homozygous: 1 bp insertion in exon 1.

Disease

Adenocarcinoma

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Complementary Products

Cell Lines & Lysates

AB265824

Human ERMP1 knockout HeLa cell line

Sanger Sequencing - Human ERMP1 knockout HeLa cell line (AB265824)

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Product details

Knockout cell lysate achieved by CRISPR/Cas9.

REACH authorisation
Abcam has not and does not intend to apply for the REACH Authorisation of customers' uses of products that contain European Authorisation list (Annex XIV) substances.
It is the responsibility of our customers to check the necessity of application of REACH Authorisation, and any other relevant authorisations, for their intended uses.

Lysate preparation: Our lysates are made using RIPA buffer to which we add a protease inhibitor cocktail and phosphatase inhibitor cocktail (ratio: 300:100:10). This means that the protein of interest is denatured. If you require a native form of the protein please use the live cell version. Please refer to our lysis protocol for further details on how our lysates are prepared.

User storage instructions: Lyophilizate may be stored at 4°C. After reconstitution, store at -20°C for short-term storage or -80°C for long-term storage.

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

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What's included?

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Properties and storage information

Gene name
ERMP1
Gene editing type
Knockout
Gene editing method
CRISPR technology
Knockout validation
Sanger Sequencing
Zygosity
Homozygous
Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C
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Supplementary information

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

ERMP1 also known as Endoplasmic Reticulum Metallopeptidase 1 is a protein that plays an important role in cellular processes. The protein has a mass of approximately 127 kDa and is widely expressed in various tissues with higher expression levels in the pancreas liver and other organs with secretory functions. ERMP1 is located in the endoplasmic reticulum where it interfaces with cellular machinery involved in protein folding and processing.
Biological function summary

ERMP1 regulates protein quality control within its cellular environment. By maintaining the integrity of protein synthesis it contributes to the proper functioning of the cellular proteome. ERMP1 is part of the endoplasmic reticulum quality control system ensuring proteins are properly folded and functional before they proceed to their destination. This protein works synergistically with other components of the cellular machinery to execute its functions effectively though it is not part of a specific protein complex.

Pathways

ERMP1 plays a significant role in the endoplasmic reticulum-associated degradation (ERAD) pathway which is essential for clearing misfolded proteins. It contributes to the ubiquitin-proteasome system interacting with proteins involved in tagging defective proteins for degradation. ERMP1 is connected to proteins such as ubiquitin ligases which are important for identifying and targeting proteins for degradation therefore ensuring cellular homeostasis and preventing stress.

ERMP1 has implications in neurodegenerative diseases and diabetes. Its ability to control protein folding and degradation is critical in these contexts. In neurodegenerative diseases such as Alzheimer's ERMP1 can influence the accumulation of misfolded proteins thereby impacting disease progression. Similarly in diabetes the disruption of ERMP1's function affects insulin production and secretion. In both cases the protein's interaction with insulin factor proteins and other signal molecules highlights its importance in disease outcomes.
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Quality control

STR analysis

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

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Cell culture

Biosafety level

EU: 2 US: 2

Adherent/suspension

Adherent

Gender

Female

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Product protocols

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Product promise

We are committed to supporting your work with high-quality reagents, and we're here for you every step of the way. In the unlikely event that one of our products does not perform as expected, you're protected by our Product Promise.
For full details, please see our Terms & Conditions

Please note: All products are 'FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC OR THERAPEUTIC PROCEDURES'.

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