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AB266823

Human OXA1L knockout HEK-293T cell line

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OXA1L KO cell line available to order. KO validated by. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, 1 bp deletion in exon 1 and 1 bp insertion in exon 1.

View Alternative Names

HSA, Mitochondrial inner membrane protein OXA1L, OXA1, OXA1-like protein, OXA1Hs, OXA1L_HUMAN, Oxidase (cytochrome c) assembly 1 like, Oxidase assembly 1-like protein

2 Images
Sanger Sequencing - Human OXA1L knockout HEK-293T cell line (AB266823)
  • Sanger seq

Unknown

Sanger Sequencing - Human OXA1L knockout HEK-293T cell line (AB266823)

Allele-2 : 1 bp deletion in exon 1.

Sanger Sequencing - Human OXA1L knockout HEK-293T cell line (AB266823)
  • Sanger seq

Unknown

Sanger Sequencing - Human OXA1L knockout HEK-293T cell line (AB266823)

Allele-1 : 1 bp insertion in exon1

Key facts

Cell type

HEK-293T

Species or organism

Human

Tissue

Kidney

Form

Liquid

form

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 1 bp deletion in exon 1 and 1 bp insertion in exon 1

Product details

Recommended control: Human wild-type HEK293T cell line (ab255449). Please note a wild-type cell line is not automatically included with a knockout cell line order, if required please add recommended wild-type cell line at no additional cost using the code WILDTYPE-TMTK1.

We will provide viable cells that proliferate on revival.

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
OXA1L
Gene editing type
Knockout
Gene editing method
CRISPR technology
Knockout validation
Sanger Sequencing
Shipped at conditions
Dry Ice
Appropriate short-term storage conditions
-196°C
Appropriate long-term storage conditions
-196°C

Handling procedures

Initial handling guidelines

Upon arrival, the vial should be stored in liquid nitrogen vapor phase and not at -80°C. Storage at -80°C may result in loss of viability.

1. Thaw the vial in 37°C water bath for approximately 1-2 minutes.
2. Transfer the cell suspension (0.8 mL) to a 15 mL/50 mL conical sterile polypropylene centrifuge tube containing 8.4 mL pre-warmed culture medium, wash vial with an additional 0.8 mL culture medium (total volume 10 mL) to collect remaining cells, and centrifuge at 201 x g (rcf) for 5 minutes at room temperature. 10 mL represents minimum recommended dilution. 20 mL represents maximum recommended dilution.
3. Resuspend the cell pellet in 5 mL pre-warmed culture medium and count using a haemocytometer or alternative cell counting method seed all remaining cells into a T25.
4. Incubate the culture at 37°C incubator with 5% CO2. Check the culture one day after revival and continue to check until 80% confluent. Media change can be given if needed.
5. Once confluent passage into an appropriate flask at a density of 2x104 cells/cm2. Seeding density is given as a guide only and should be scaled to align with individual lab schedules. Cultures should be monitored daily.

Subculture guidelines
  • All seeding densities should be based on cell counts gained by established methods.
  • A guide seeding density of 2x104 cells/cm2 is recommended.
  • Cells should be passaged when they have achieved 80-90% confluence.
Culture medium

DMEM (High Glucose) + 10% FBS

Cryopreservation medium

Cell Freezing Medium-DMSO Serum free media, contains 8.7% DMSO in MEM supplemented with methyl cellulose.

Supplementary information

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

OXA1L also known as mitochondrial inner membrane protein OXA1L functions mechanically in the insertion and assembly of proteins in the mitochondrial inner membrane. This protein with a mass of approximately 45 kDa localizes to the mitochondria and exhibits broad tissue expression. OXA1L plays a role in protein translocation specifically contributing to the insertion of multi-spanning membrane proteins coming from the mitochondrial ribosomes.
Biological function summary

OXA1L facilitates the integration of proteins into the mitochondrial inner membrane essential for maintaining mitochondrial function and biogenesis. OXA1L operates as part of a larger complex that assists protein assembly and stabilization. Such interactions highlight its role in mitochondrial respiratory chain assembly necessary for maintaining cellular energy balance.

Pathways

OXA1L integrates specifically into the pathway of mitochondrial oxidative phosphorylation. This target works alongside important proteins like COX1 and COX2 shaping the proper assembly of components of the electron transport chain. Additionally OXA1L interacts with the mitochondrial import machinery vital for maintaining the efficiency of protein import pathways that regulate cellular respiration.

Mutations or dysregulation of OXA1L correlate with mitochondrial disorders and neurological diseases including sensorineural hearing loss and mitochondrial complex I deficiency. NDUFAF2 involved in complex I assembly shows interaction with OXA1L in these conditions highlighting a shared pathway that can lead to disrupted energy production and neurological symptoms.

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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