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AB259144

Human SMIM4 (C3orf78) knockout HeLa cell lysate

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UQCC5 KO cell lysate available now. KO validated. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon1 and Insertion of the selection cassette in exon1.
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Sanger Sequencing - Human SMIM4 (C3orf78) knockout HeLa cell lysate (AB259144)
  • Sanger seq

Unknown

Sanger Sequencing - Human SMIM4 (C3orf78) knockout HeLa cell lysate (AB259144)

Allele-2 : Insertion of the selection cassette in exon1

Sanger Sequencing - Human SMIM4 (C3orf78) knockout HeLa cell lysate (AB259144)
  • Sanger seq

Unknown

Sanger Sequencing - Human SMIM4 (C3orf78) knockout HeLa cell lysate (AB259144)

Allele-1 : 1 bp insertion in exon1

Key facts

Cell type

HeLa

Species or organism

Human

Tissue

Cervix

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon1 and Insertion of the selection cassette in exon1.

Disease

Adenocarcinoma

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.

What's included?

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Properties and storage information

Gene name
UQCC5
Gene editing type
Knockout
Gene editing method
CRISPR technology
Knockout validation
Sanger Sequencing
Shipped at conditions
Ambient - Can Ship with Ice
Appropriate short-term storage conditions
-20°C
Appropriate long-term storage conditions
-20°C

Supplementary information

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

C3orf78 also known as Chromosome 3 Open Reading Frame 78 is a protein with a molecular weight of approximately 80 kDa. This protein exhibits expression in various tissues but data on specific cell types remain limited. Mechanically C3orf78 functions as a protein with potential regulatory roles in cells although detailed molecular mechanisms are still under investigation. Current research suggests interactions with other cellular components hinting at complex roles yet to be fully elucidated.
Biological function summary

C3orf78 plays a part in cellular processes that may involve interactions with other proteins as part of a larger complex. Its exact biological role remains under investigation but initial studies suggest it may influence cellular homeostasis and signaling. C3orf78's expression in diverse tissue types implies involvement in multiple physiological functions possibly affecting normal cellular activities through regulatory mechanisms and interactions with yet unidentified partners.

Pathways

Research has positioned C3orf78 within cellular signaling pathways potentially influencing cellular responses. Its connections in the Ras signaling pathway suggest associations with cell growth and differentiation processes. Also C3orf78 could relate to the PI3K-AKT pathway known to be critical for cell survival. Interactions with related signaling proteins such as KRAS and PI3K might affect these pathways highlighting its potential role in modulating cellular events.

Mutations or dysregulation of C3orf78 may contribute to the development of cancer and neurological diseases. While direct evidence remains sparse its involvement in cancer is hypothesized through interactions with oncogenes like KRAS. Additionally in neurological contexts abnormal C3orf78 expression may engage with pathways related to proteins like mTOR impacting neurodegenerative processes. Continued research aims to clarify its role in these pathological conditions and validate these initial associations.

Quality control

STR analysis

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

Cell culture

Biosafety level

EU: 2 US: 2

Adherent/suspension

Adherent

Gender

Female

Product protocols

Product promise

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