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Phospho-LATS1 (Thr1079) (D57D3

) Rabbit mAb
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  • 询价
  • Cell Signaling Technology已认证
  • USA
  • 2025年11月16日
  • W
  • H,M,R,Mk
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    • 详细信息
    • 文献和实验
    • 技术资料
    • 抗体英文名

      Phospho-LATS1 (Thr1079) (D57D3) Rabbit mAb

    • 抗原

      synthetic phosphopeptide corresponding to residues surrounding Thr1079 of human LATS1 protein

    • 应用范围

      W

    • 库存

      大量

    • 供应商

      CST

    • 适应物种

      H,M,R,Mk

    • 保质期

      详见说明书

    • 级别

      详见MSDS文件

    • 是否单克隆

      1

    • 保存条件

      -20°c

    • 规格

      100 ul (10 western blots)/carrier free & custom formulation / quantity

    规格:产品价格:¥请询价
    规格:100 ul (10 western blots)产品价格:¥请询价
    规格:carrier free & custom formulation / quantity产品价格:¥请询价

    pathway more info application references datasheet PDF MSDS PDF protocols

    Applications Key:  W=Western Blotting
    Reactivity Key:  H=Human  M=Mouse  R=Rat  Mk=Monkey
    Species cross-reactivity is determined by western blot. Species enclosed in parentheses are predicted to react based on 100% sequence homology.

    Applications Reactivity Sensitivity MW (kDa) Isotype
    W H (M) (R) (Mk) Endogenous 140 Rabbit IgG
    Protocols
    Specificity / Sensitivity

    Phospho-LATS1 (Thr1079) (D57D3) Rabbit mAb detects endogenous levels of LATS1 protein only when phosphorylated at Thr1079. This antibody is predicted to cross react with LATS2 only when LATS2 is phosphorylated at Thr1041.

    Source / Purification

    Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Thr1079 of human LATS1 protein.

    Western Blotting

    Western Blotting

    Western blot analysis of extracts from HeLa cells, untreated (-) or okadaic acid-treated (+), using Phospho-LATS1 (Thr1079) (D57D3) Rabbit mAb (upper) or LATS1 (C66B5) Rabbit mAb #3477 (lower).

    Background

    LATS1 (Large tumor suppressor 1) is a putative serine/threonine kinase that belongs to the NDR family (1). It is a tumor suppressor that plays a critical role in the maintenance of ploidy. LATS1 localizes to the centrosome and the mitotic spindle and controls G2/M transition by negatively regulating cdc2 kinase activity (2,3). LATS1 also plays a role in the G1 tetraploidy checkpoint via control of p53 expression (4).LATS1 affects cytokinesis by regulating actin polymerization through negative modulation of LIMK1 (5). LATS1 also binds the phosphorylated form of zyxin, a regulator of actin filament assembly. This interaction promotes localization of zyxin to the mitotic spindle, suggesting a role for actin regulatory proteins during mitosis (6). Decreased expression is associated with breast tumor aggressiveness (7), promoter methylation, and loss of heterozygosity. Mutations perturbing LATS1 have been associated with human sarcomas and ovarian sarcomas (8,9). LATS1 knock out mice develop soft-tissue sarcomas, ovarian stromal cell tumor, and display a high sensitivity to carcinogenic treatments (10).Human LATS1 exists in a complex similar to the Drosophila Hippo/Salvador/Lats tumor suppressor network, a complex that regulates proliferation and apoptosis to control growth and shape of the fly. The corresponding human complex contains Hippo and Salvador homologs RASSF1A, WW45, and MST2 and may control mitotic exit (11).Many molecules have been discovered that are involved in the Hippo pathway, but mechanisms governing activation of these proteins and activation of the pathway in general are currently not clear. Phosphorylation of LATS1 and LATS2 is stimulated by association with Mob1, which is itself phosphorylated by Mst1/2 (12,13). Phosphorylation of LATS1/2 is required for activation of YAP, a key mediator of the Hippo signaling pathway (14).

    1. Tao, W. et al. (1999) Nat Genet 21, 177-81.
    2. Yang, X. et al. (2001) Oncogene 20, 6516-23.
    3. Xia, H. et al. (2002) Oncogene 21, 1233-41.
    4. Iida, S. et al. (2004) Oncogene 23, 5266-74.
    5. Yang, X. et al. (2004) Nat Cell Biol 6, 609-17.
    6. Hirota, T. et al. (2000) J Cell Biol 149, 1073-86.
    7. Morinaga, N. et al. (2000) Int J Oncol 17, 1125-9.
    8. Hansen, L.L. et al. (2002) Cancer Genet Cytogenet 139, 1-8.
    9. Hisaoka, M. et al. (2002) Lab Invest 82, 1427-35.
    10. St John, M.A. et al. (1999) Nat Genet 21, 182-6.
    11. Guo, C. et al. (2007) Curr Biol 17, 700-5.
    12. Hergovich, A. et al. (2006) Biochem Biophys Res Commun 345, 50-8.
    13. Hirabayashi, S. et al. (2008) Oncogene 27, 4281-92.
    14. Zhao, B. et al. (2010) J Cell Sci 123, 4001-6.
    Application References

    Have you published research involving the use of our products? If so we'd love to hear about it. Please let us know !

    Companion Products

    For Research Use Only. Not For Use In Diagnostic Procedures.

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    • 三生三世,一场组化,一次豪赌

      h)即可。2. 修复大法——不仅仅是「煮一煮」微波炉修复:简单易行效果好,CST 推荐使用微波炉完成修复。合适的修复液:根据抗体说明书使用合适的修复液。用柠檬酸修复后,切片需浸泡在修复液中,自然冷却;而用 EDTA 修复后,切片可直接从修复缸中取出,直接进行下一步。注:使用不同的修复方式和不同生产商的抗体检测人肺癌组织中 EGFR 的表达。第一排为 CST 的 EGF Receptor (D38B1) XP® Rabbit mAb(#4267),EDTA 的修复方式明显优于柠檬酸盐及胃蛋白

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