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AB264733

Human SCN1B knockout HeLa cell line

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SCN1B KO cell line available to order. KO validated by. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, 106 bp insertion in exon 2 and 1 bp deletion in exon 2.

View Alternative Names

GEFSP1, SCN1B_HUMAN, Sodium channel subunit beta-1, Sodium channel voltage gated type I beta, Sodium channel voltage gated type I beta subunit, sodium channel beta 1 subunit

2 Images
Sanger Sequencing - Human SCN1B knockout HeLa cell line (AB264733)
  • Sanger seq

Unknown

Sanger Sequencing - Human SCN1B knockout HeLa cell line (AB264733)

Allele-1 : 1 bp deletion in exon 2.

Sanger Sequencing - Human SCN1B knockout HeLa cell line (AB264733)
  • Sanger seq

Unknown

Sanger Sequencing - Human SCN1B knockout HeLa cell line (AB264733)

Allele-2 : 106 bp insertion in exon 2.

Key facts

Cell type

HeLa

Species or organism

Human

Tissue

Cervix

Form

Liquid

form

Knockout validation

Sanger Sequencing

Mutation description

Knockout achieved by using CRISPR/Cas9, 106 bp insertion in exon 2 and 1 bp deletion in exon 2

Disease

Adenocarcinoma

Product details

Recommended control: Human wild-type HeLa cell line (ab255928). 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
SCN1B
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.

SCN1B also known as sodium channel beta-1 subunit mechanically functions as an accessory protein to voltage-gated sodium channels. It is a protein with a mass of approximately 22 kDa. SCN1B modulates the function of these channels including their kinetics and cell surface expression. This protein is expressed predominantly in the central and peripheral nervous systems but can also be found in other tissues like the heart.
Biological function summary

The sodium channel beta-1 subunit participates in the initiation and propagation of action potentials. It forms part of the sodium channel complex contributing structural stability and influencing the gating properties of the channel. SCN1B interacts with alpha subunits of sodium channels and other beta subunits which allow it to regulate the excitability of neurons and cardiac myocytes. It plays a critical role in maintaining the electrical signaling within these cells.

Pathways

The activity of SCN1B contributes significantly to the regulation of neuronal firing and cardiac rhythm. It is involved in the voltage-gated sodium channel complex which is an important player in the excitation-contraction coupling pathway and neuronal excitability pathways. SCN1B modulates the activity of related proteins such as SCN8A the sodium channel protein type 8 subunit alpha within these pathways influencing their function in electrical signaling processes.

Mutations or dysfunctions in SCN1B can lead to diseases such as epilepsy and cardiac arrhythmias. Such conditions may result from altered sodium channel function caused by mutations in SCN1B that impact the excitability of neurons or cardiac muscles. For instance it connects to proteins like SCN1A another sodium channel subunit which also is involved in disorders such as Dravet syndrome. These conditions highlight the importance of SCN1B in maintaining normal neurophysiological and cardiac functions.

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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