您现在的位置: 首页   -  产品中心   -  免疫学   -   抗体
Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb (S-1874-69)

Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb (S-1874-69)

货号: S0B1465
价格: 600
规格: 25μl
介绍: -
其他: -
产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    Phospho-LATS1/2(Ser909/872)
  • 分子别名

    Serine/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
  • 免疫原

    Synthetic Peptide
  • 细胞定位

    Endoplasmic reticulum
  • Accession

    O95835, Q9NRM7
  • 克隆号

    S-1874-69
  • 抗体类型

    Recombinant mAb
  • 抗体同种型

    IgG
  • 应用

    ICC, WB
  • 反应种属 ?

    Hu, Ms
  • 阳性样本

    HeLa treated with 100 ng/ml Calyculin A for 30 minutes, serum-starved NIH/3T3 treated with 100 nM Calyculin A for 30 minutes
  • 纯化方式

    Protein A
  • 浓度

    0.5 mg/ml
  • 标记

    Unconjugated
  • 性状

    Liquid
  • 缓冲体系

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

  • 储存条件

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

稀释度
应用 稀释度 推荐种属
Dot Blot 1:1000
WB 1:1000 Hu, Ms
ICC 1:500 Hu
背景介绍
  • 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.

  • 免疫印迹

    • WB result of Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb
      Primary antibody: Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: untreated HeLa whole cell lysate 20 µg
      Lane 2: HeLa treated with 100 ng/ml Calyculin A for 30 minutes whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 127, 120 kDa
      Observed MW: 140, 120 kDa

    • WB result of Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb
      Primary antibody: Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb at 1/1000 dilution
      Lane 1: untreated NIH/3T3 whole cell lysate 20 µg
      Lane 2: serum-starved NIH/3T3 treated with 100 nM Calyculin A for 30 minutes whole cell lysate 20 µg
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 127, 120 kDa
      Observed MW: 130, 115 kDa

  • 斑点杂交

    • Dot blot result of Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb
      Lane 1: LATS1/2(Ser909/872) phospho peptide
      Lane 2: LATS1/2(Ser909/872) unmodified peptide
      Primary antibody: Phospho-LATS1/2(Ser909/872) Recombinant Rabbit mAb at 1/1000 dilution
      Secondary antibody: Goat Anti-rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution

  • 免疫细胞化学

    • ICC analysis of HeLa cells treated with 100 ng/ml Calyculin A for 30 minutes (top panel) and untreated HeLa cells (below panel). Anti- Phospho-LATS1/2(Ser909/872) antibody was used at 1/500 dilution (Green) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 488) was used as secondary antibody at 1/1000 dilution. The cells were fixed with 4% PFA and permeabilized with 0.1% PBS-Triton X-100. Nuclei were counterstained with DAPI (Blue). Counterstain with tubulin (Red).