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AB263295

Human PIGT knockout HEK-293T cell lysate

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PIGT KO cell lysate available now. KO validated. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 1 bp deletion in exon 1 and 5 bp deletion in exon 1.
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Sanger Sequencing - Human PIGT knockout HEK-293T cell lysate (AB263295)
  • Sanger seq

Unknown

Sanger Sequencing - Human PIGT knockout HEK-293T cell lysate (AB263295)

Allele-1 : 5 bp deletion in exon 1

Sanger Sequencing - Human PIGT knockout HEK-293T cell lysate (AB263295)
  • Sanger seq

Unknown

Sanger Sequencing - Human PIGT knockout HEK-293T cell lysate (AB263295)

Allele-2 : 1 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, 1 bp deletion in exon 1 and 5 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
PIGT
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.

PIGT (Phosphatidylinositol Glycan Anchor Biosynthesis Class T) plays a mechanical role in the biosynthesis of glycosylphosphatidylinositol (GPI) anchors. Also known as PIG-T this protein is part of the GPI transamidase complex and has a molecular mass of approximately 68 kDa. It resides in the endoplasmic reticulum where it supports the attachment of various proteins to the cell membrane through GPI anchoring. PIGT is ubiquitously expressed across different human tissues indicating its fundamental role in cellular physiology.
Biological function summary

PIGT acts as a subunit within the GPI transamidase complex that enhances the transfer of pre-assembled GPI units to proteins. This activity anchors proteins to the cell surface which is necessary for their stability and function. The GPI anchor allows effective signaling adhesion and protection of proteins impacting many cellular processes. The interdependency with other subunits such as PIGA PIGK and PIGS ensures the complete function of the GPI transamidase complex.

Pathways

PIGT remains key within the GPI-anchor biosynthesis pathway playing a critical role in cell surface protein localization. It interacts with other members like PIGU and GAA1 within this pathway forming interactions necessary for proper transit and attachment of GPI-anchored proteins. The functionality of the GPI-anchor pathway directly influences cellular communication through pathways like signal transduction which are essential for different biological processes.

Mutations or deficiencies in PIGT link to Paroxysmal Nocturnal Hemoglobinuria (PNH) and Early Infantile Epileptic Encephalopathy (EIEE). PNH involves defective GPI-anchored proteins affecting the regulation of cell membrane stability while EIEE relates to neurological complications due to disturbed protein functioning. PIGT connects with other proteins like PIGM and PIGL contributing to the disorders' pathophysiology when disruptions in GPI-anchor biosynthesis occur.

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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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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