Alexa Fluor® 647 anti-PTEN Phospho (Ser380) Antibody, PTEN, A22005D,BioLegend,626453

For use of this antibody (clone A22005D) in intracellular staining in flow cytometry (ICFC), we recommend using True-Phos ™ Perm Buffer (Cat. No. 425401) for fixation/permeabilization.For use of this antibody (clone A22005D) in immunohistochemistry on FFPE tissues (IHC-P), we recommend antigen retrieval with Tris-EDTA pH 9.0 Buffer (Cat. No. 422703).

Host

Mouse

Reactivity

Human

Application

ICFC - Quality testedIHC-P - Verified

Platform ID

BAB053541168

BioLegend

Headquarters

8999 BioLegend Way San Diego, CA 92121 United States

Contact

Tel: 1-858-455-9588
Fax: +49 (4131) 7023913

Email:

Product Specifications
Scientific Background

Specifications

NameAlexa Fluor® 647 anti-PTEN Phospho (Ser380) Antibody, PTEN, A22005D
Cat. No.626453
HostMouse
RRIDAB_3662411 (BioLegend Cat. No. 626453)
IsotypeMouse IgG1, κ
ReactivityHuman
ApplicationICFC - Quality testedIHC-P - Verified
ClonalityMonoclonal
Clone NumberA22005D
Concentration0.5 mg/mL
TargetPTEN Phospho Ser380
ImmunogenSynthetic peptide from human PTEN phosphorylated at Serine 280
PurityThe antibody was purified by affinity chromatography and conjugated with Alexa Fluor® 647 under optimal conditions.
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide
StorageThe antibody solution should be stored undiluted between 2°C and 8°C, and protected from prolonged exposure to light.Do not freeze.
Regulatory StatusResearch Use Only

Scientific Background

PTEN is a tumor suppressor gene which encodes a phosphatase that preferentially dephosphorylates phosphoinositide substrates and thereby modulates cell cycle progression and cell survival. PTEN is an important negative regulator of the PI3K/AKT/mTOR signaling pathway by dephosphorylating PIP3. PTEN is commonly mutated in human cancer, hence, loss of expression/function of PTEN due to mutations have been observed in prostate cancer, glioblastoma, endometrial, lung and breast cancers. Other non-cancerous clinical disorders associated with PTEN mutation are Cowden syndrome, Bannayan-Riley-Ruvalcaba syndrome, and proteus-like syndrome. PTEN is phosphorylated at several residues and some lead to increase in activity while others lead to loss of function and degradation. Specifically, phosphorylation at serine 380 residue by casein kinase 2 (CK2), leads to degradation of PTEN in the proteasome.

Category Paths

Request a product

Please provide the required information below so that we can quickly source your products.