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Phospho-LATS1 (Thr1079) Polyclonal antibody

Phospho-LATS1 (Thr1079) Polyclonal Antibody for WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human and More (2)

Applications

WB, IHC, IF, ELISA

LATS1 (phospho T1041), LATS1 (Thr1079), p LATS1 , p LATS1 (Thr1041), p LATS1 (Thr1079)

Formulation:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 
SKU: 

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Tested Applications

Positive WB detected inCalyculin A treated HeLa cells

The antibody also detects the phosphorylated at Thr1041 of the LATS2.

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:5000-1:50000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

28998-1-AP targets Phospho-LATS1 (Thr1079) in WB, IHC, IF, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Cited Reactivityhuman, mouse, rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

Peptide

Predict reactive species
Full Name LATS, large tumor suppressor, homolog 1 (Drosophila)
Calculated Molecular Weight 15 kDa, 127 kDa
Observed Molecular Weight140-150 kDa
GenBank Accession NumberBC015665
Gene Symbol LATS1
Gene ID (NCBI) 9113
RRIDAB_2923586
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity purification
UNIPROT IDQ6PJG3
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

The large tumour suppressor 1 (LATS1) acting as a tumour suppressor is a serine/threonine kinase of the AGC kinase family and is found to be down-regulated in various types of human cancers. Recently, LATS1 has been identified as a central player of the emerging tumour suppressive Hippo signaling pathway. In this pathway, the MST1/2 kinase phosphorylates activates LATS1/2 which, together with its co-factor MOB1, subsequently phosphorylates and inhibits the YAP transcriptional factor by preventing them from translocating to the nucleus. The antibody also detects the phosphorylated at Thr1041 of the LATS2. (PMID: 32460168, PMID: 30219064,PMID: 31792377)

Protocols

Product Specific Protocols
WB protocol for Phospho-LATS1 (Thr1079) antibody 28998-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

What published studies show

Phospho-LATS1 (Thr1079) Polyclonal antibody (Cat# 28998-1-AP) has 35 citations published in journals including Journal of Advanced Research, Advanced Science, Molecular Biomedicine, Cell Death & Disease, International Journal of Biological Sciences, Journal of Translational Medicine, Radiotherapy and Oncology, and Drug Design, Development and Therapy. Research fields span cancer biology (lung, liver, renal, ovarian, colorectal), Hippo-YAP signaling, fibrosis, mechanobiology, cardiac pathology, and environmental toxicology.

SpeciesApplicationTitle
human,mouseWB

J Adv Res

Matrix stiffness drives squamous cell carcinoma progression via a Piezo1-mediated mechanotransduction feedback loop.

Authors - Zixi Jiang

Adv Sci (Weinh)

The E3 Ligase RNF115 Aggravates Pathological Cardiac Hypertrophy via Ubiquitin-Mediated Degradation of SPTBN1.

Authors - Yan Zu
humanWB

Mol Biomed

The EZH2 selective inhibitor ZLD1039 attenuates UUO-induced renal fibrosis by suppressing YAP activation

Authors - Qingling Xia
humanWB

Cell Death Dis

PLAGL2 promotes bladder cancer progression via RACGAP1/RhoA GTPase/YAP1 signaling

Authors - Hualin Chen
humanWB

Cell Mol Biol Lett

KIAA1429-mediated m6A modification of CHST11 promotes progression of diffuse large B-cell lymphoma by regulating Hippo-YAP pathway

Authors - Xiaomin Chen
humanWB

Int J Biol Sci

S100 Calcium Binding Protein A16 Promotes Cell Proliferation by triggering LATS1 ubiquitin degradation mediated by CUL4A ligase to inhibit Hippo pathway in Glioma development

Authors - Yifang Hu
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