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AB263420

Human WDR83OS (C19orf56) knockout HEK-293T cell lysate

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WDR83OS KO cell lysate available now. KO validated by. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 7 bp deletion in exon 1 and 8 bp deletion in exon 1.

View Alternative Names

C19orf56, CS056_HUMAN, Chromosome 19 open reading frame 56, Hypothetical protein LOC51398, PTD008, UPF0139 membrane protein C19orf56

2 Images
Sanger Sequencing - Human WDR83OS (C19orf56) knockout HEK-293T cell lysate (AB263420)
  • Sanger seq

Unknown

Sanger Sequencing - Human WDR83OS (C19orf56) knockout HEK-293T cell lysate (AB263420)

Allele-2 : 7 bp deletion in exon 1

Sanger Sequencing - Human WDR83OS (C19orf56) knockout HEK-293T cell lysate (AB263420)
  • Sanger seq

Unknown

Sanger Sequencing - Human WDR83OS (C19orf56) knockout HEK-293T cell lysate (AB263420)

Allele-1 : 8 bp deletion in exon 1

Key facts

Cell type

HEK-293T

Species or organism

Human

Tissue

Kidney

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 7 bp deletion in exon 1 and 8 bp deletion in exon 1.

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 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.

What's included?

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Properties and storage information

Gene name
WDR83OS
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.

C19orf56 also known as MONA or INIP functions as an important player in DNA repair processes specifically homologous recombination. It has a molecular weight of approximately 26 kDa. This protein shows expression across various tissues but appears more prominently in the testis and thymus. As part of DNA repair machinery C19orf56 participates in maintaining genome stability by facilitating accurate DNA exchange during cell division.
Biological function summary

The maintenance of genome integrity involves the activity of C19orf56. C19orf56 operates within the DNA damage response and associates with other components to form repair complexes. It is necessary for effective repair of double-strand breaks which protects cells from accumulating mutations. The protein acts in coordination with diverse repair enzymes and structural proteins to detect and correct DNA damage ensuring genomic stasis.

Pathways

C19orf56 serves an essential role in the homologous recombination repair pathway. It interacts closely with proteins like RAD51 an important partner within this pathway. The protein also contributes to the DNA damage signaling pathway where it may interact with p53 an important regulator of the cell cycle and apoptosis. This shows the protein's function in important cellular mechanisms governing cell division and stability.

C19orf56 shows connections to conditions like cancer and Fanconi anemia. Alterations in its function can lead to genomic instability increasing cancer susceptibility. Its interaction with BRCA1 indicates a potential impact on breast cancer pathology where ineffective repair pathways may facilitate oncogenic transformations. Also defects in C19orf56 have associations with impaired bone marrow function seen in Fanconi anemia linking the protein to hematopoietic disorders.

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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