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AB266136

Human SH2B2 (APS) knockout HEK-293T cell line

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SH2B2 KO cell line available to order. KO validated by. Free of charge wild type control provided. Knockout achieved by using CRISPR/Cas9, 1 bp insertion in exon 2 and Insertion of the selection cassette in exon 2.

View Alternative Names

Adaptor protein with pleckstrin homology and src homology 2 domains, SH2 and PH domain containing adapter protein APS

2 Images
Sanger Sequencing - Human SH2B2 (APS) knockout HEK-293T cell line (AB266136)
  • Sanger seq

Unknown

Sanger Sequencing - Human SH2B2 (APS) knockout HEK-293T cell line (AB266136)

Allele-2 : 1 bp insertion in exon 2.

Sanger Sequencing - Human SH2B2 (APS) knockout HEK-293T cell line (AB266136)
  • Sanger seq

Unknown

Sanger Sequencing - Human SH2B2 (APS) knockout HEK-293T cell line (AB266136)

Allele-1 : Insertion of the selection cassette in exon2

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 insertion in exon 2 and Insertion of the selection cassette in exon 2

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
SH2B2
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.

APS also known as SH2B adapter protein 2 acts as an adaptor in various signaling pathways. It is a protein with a mass of approximately 80 kDa. The APS is expressed in many tissues but largely found in the spleen and brain. It features an SH2 domain and plays a significant role in modulating signaling cascades.
Biological function summary

APS participates in cell signaling by linking activated receptors to downstream signaling proteins. It often associates with receptor tyrosine kinases such as the insulin receptor. APS can form part of a larger complex with these kinases influencing cellular processes like glucose lipid metabolism and growth. APS interactions are essential for transducing signals that affect metabolic and growth pathways.

Pathways

APS is notably involved in the insulin signaling pathway and the JAK-STAT pathway. In insulin signaling APS supports insulin receptor functions by promoting the recruitment of key proteins such as PI3K and Akt which are important for glucose uptake and lipid synthesis. In the JAK-STAT pathway APS acts by facilitating interactions with the JAK family of kinases which affects gene expression and immune responses.

APS associations connect it to metabolic conditions and cancer. Altered APS expression or function can affect insulin signaling contributing to insulin resistance and type 2 diabetes. In cancer abnormal APS interactions might play a role in signaling pathways that lead to tumor growth. APS links to proteins like IRS1 in diabetes which alters glucose metabolism and STAT proteins in cancer impacting cell proliferation and survival.

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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