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Home >Products> Reagents >Antibody> Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb (S-1874-69)
Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb (S-1874-69)
Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb (S-1874-69)
Origin of place Singapore
Model S0B1465-25μl
Supplier ANT BIO PTE.LTD.
Price 100
Hits 10
Updated 9/1/2025
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Product Specification


HostRabbit
AntigenPhospho-LATS1/2(Ser909/872)
SynonymsSerine/threonine-protein kinase LATS1; Large tumor suppressor homolog 1; WARTS protein kinase (h-warts); WARTS; Serine/threonine-protein kinase LATS2; Kinase phosphorylated during mitosis protein; Large tumor suppressor homolog 2; Serine/threonine-protein kinase kpm; Warts-like kinase; KPM
ImmunogenSynthetic Peptide
LocationEndoplasmic reticulum
AccessionO95835銆?Q9NRM7
Clone NumberS-1874-69
Antibody TypeRecombinant mAb
IsotypeIgG
ApplicationWB, ICC
ReactivityHu, Ms
Positive SampleHeLa treated with 100 ng/ml Calyculin A for 30 minutes, serum-starved NIH/3T3 treated with 100 nM Calyculin A for 30 minutes
PurificationProtein A
Concentration0.5 mg/ml
ConjugationUnconjugated
Physical AppearanceLiquid
Storage Buffer

PBS, 40% Glycerol, 0.05% BSA, 0.03% Proclin 300

Stability & Storage

12 months from date of receipt / reconstitution, -20 掳C as supplied

Dilution


applicationdilutionspecies
Dot Blot1:1000
WB1:1000Hu, Ms
ICC1:500Hu

Background

Phospho-LATS1/2(Ser909/872) refers to the phosphorylated forms of the mammalian Hippo signaling pathway kinases LATS1 (Large Tumor Suppressor 1) and LATS2 at specific serine residues (Ser909 in LATS1 and Ser872 in LATS2). As core components of this pathway, LATS1/2 are activated through phosphorylation by upstream kinases MST1/2, which subsequently phosphorylate downstream effector proteins YAP/TAZ to regulate their nucleocytoplasmic shuttling, degradation, and biological functions, thereby suppressing cell proliferation and promoting apoptosis. Phosphorylation at Ser909/872 is likely a critical step in LATS1/2 activation, potentially modulating their kinase activity, stability, or interactions with regulatory proteins. This phosphorylation event is commonly used as a biomarker of Hippo pathway activity, detectable via specific antibodies (e.g., in Western blotting), and is studied in contexts such as cancer and organ development due to the pathway's strong association with tumorigenesis and metastasis. Notably, species-specific variations or splice isoforms may alter residue numbering, and functional validation often involves mutagenesis experiments (e.g., phosphomimetic glutamic acid substitutions or non-phosphorylatable alanine mutations) to assess impacts on pathway regulation.

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