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AB259139

Human SLC5A6 knockout HEK-293T cell lysate

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SLC5A6 KO cell lysate available now. KO validated. Free of charge wild type control included. Knockout achieved by using CRISPR/Cas9, 1 bp deletion in exon3 and 7 bp deletion in exon3.
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Sanger Sequencing - Human SLC5A6 knockout HEK-293T cell lysate (AB259139)
  • Sanger seq

Unknown

Sanger Sequencing - Human SLC5A6 knockout HEK-293T cell lysate (AB259139)

Allele-1 : 7 bp deletion in exon3

Sanger Sequencing - Human SLC5A6 knockout HEK-293T cell lysate (AB259139)
  • Sanger seq

Unknown

Sanger Sequencing - Human SLC5A6 knockout HEK-293T cell lysate (AB259139)

Allele-2 : 1 bp deletion in exon3

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 exon3 and 7 bp deletion in exon3.

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
SLC5A6
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.

SLC5A6 also known as the sodium-dependent multivitamin transporter (SMVT) mechanically functions as a transmembrane protein responsible for the uptake of vital water-soluble vitamins and cofactors such as biotin pantothenic acid and lipoate. The protein has an approximate molecular mass of 72 kDa. It is expressed in various tissues with high levels observed in the intestines kidneys and placenta indicating its role in nutrient absorption and metabolic processes.
Biological function summary

SLC5A6 is essential for the efficient transport of vitamins across cell membranes using sodium gradient as the driving force. It transports vitamins into cells where they participate as coenzymes in several enzymatic reactions. This transporter does not form part of a larger protein complex but functions individually to link dietary intake with cellular nutrient requirements. The absorption through SLC5A6 impacts various biosynthetic processes as biotin and pantothenate contribute to fatty acid synthesis and energy metabolism.

Pathways

The role of SLC5A6 in nutrient absorption connects it to critical metabolic pathways such as the biotin and CoA biosynthetic pathways. Its function impacts cellular metabolism by providing essential cofactors for carboxylation reactions and energy production. SLC5A6 interacts with enzymes that rely on these vitamin-derived cofactors maintaining cellular metabolic equilibrium essential for cell growth and energy balance.

Mutations or dysfunction in SLC5A6 can lead to conditions like biotinidase deficiency which results in various neurological and dermatological symptoms. There are connections between SLC5A6 malfunctions and certain metabolic disorders due to impaired nutrient uptake linking this transporter to proteins involved in biotin metabolism. Research indicates possible associations of SLC5A6 with neurological disorders as biotin deficiency impacts brain functions and development.

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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