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AB267156

Human MSX1 knockout A549 cell line

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MSX1 KO cell line available to order. KO validated by. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, Homozygous: 10 bp deletion in exon 1.

View Alternative Names

AA675338, AI324650, HYD 1, Homeobox 7, Homeobox protein Hox-7, Homeobox protein MSX-1, Homeobox, msh-like 1, Hox 7.1, Hox-7, MSH, MSH, Drosophila, Homolog of, 1, MSX1_HUMAN, Msh homeobox 1, Msh homeobox 1-like protein, Muscle segment homeobox, Muscle segment homeobox, Drosophila, Homolog of, 1, OFC5, OTTHUMP00000115387, STHAG1, msh (Drosophila) homeo box homolog 1 (formerly homeo box 7), msh homeo box homolog 1, msh homeobox homolog 1 (Drosophila)

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Sanger Sequencing - Human MSX1 knockout A549 cell line (AB267156)
  • Sanger seq

Unknown

Sanger Sequencing - Human MSX1 knockout A549 cell line (AB267156)

Homozygous : 10 bp deletion in exon1

Key facts

Cell type

A549

Species or organism

Human

Tissue

Lung

Form

Liquid

form

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, Homozygous: 10 bp deletion in exon 1

Disease

Carcinoma

Product details

Recommended control: Human wild-type A549 cell line (ab255450). 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 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
MSX1
Gene editing type
Knockout
Gene editing method
CRISPR technology
Knockout validation
Sanger Sequencing
Zygosity
Homozygous
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.
  • Do not allow the cell density to exceed 7x104 cells/cm2.
Culture medium

F-12K + 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.

The MSX1 protein sometimes called Homeobox protein MSX-1 is a transcription factor with a mass of approximately 33 kDa. It plays a role in the regulation of embryonic development by controlling the expression of several genes. This protein is mainly expressed in tissues such as the limb buds craniofacial regions and developing teeth which are critical sites for its function during different stages of growth.
Biological function summary

MSX1 modulates a variety of developmental processes including craniofacial morphogenesis and limb formation. It operates as part of a DNA-binding complex that influences the transcription of target genes essential for proper tissue differentiation and formation. Through its activity MSX1 affects cell proliferation and apoptosis ensuring the accurate development of specific structures in the organism.

Pathways

MSX1 interacts with the WNT signaling and bone morphogenetic protein (BMP) pathways. In the WNT signaling pathway MSX1 modulates the expression of genes involved in the regulation of developmental processes and cell fate determination. It also interacts with BMP-related proteins playing an important role in skeletal formation and patterning demonstrating connections with other proteins like BMP4 and LEF1.

MSX1 has been implicated in the development of tooth agenesis and craniosynostosis. Research shows that mutations in the MSX1 gene can lead to these conditions affecting the normal formation and differentiation of skeletal elements. Furthermore MSX1 has connections with the protein PAX9 as together they contribute to the regulation of dental development and disruptions in their interactions often result in anomalies in tooth formation.

Quality control

STR analysis

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

Cell culture

Biosafety level

EU: 1 US: 1

Adherent/suspension

Adherent

Gender

Male

Product protocols

Product promise

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