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LAG3 Recombinant Rabbit mAb,PBS Only (SDT-R159)

Lymphocyte activation gene 3 protein

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货号 S0B2170P
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产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    LAG3
  • 分子别名

    Lymphocyte activation gene 3 protein
  • 细胞定位

    Cell membrane
  • Accession

    P18627
  • 克隆号

    SDT-R159
  • 抗体类型

    Recombinant mAb
  • 反应种属 ?

    Hu
  • 纯化方式

    Protein A
  • 浓度

    1 mg/ml
  • 性状

    Liquid
  • 缓冲体系

    PBS

  • 储存条件

    12 months from date of receipt, 4°C as supplied

  • 应用

    IHC-P ?

    IF ?

  • 稀释度

    应用 稀释度
    IHC-P 1:1000
    IF 1:500
背景介绍
  • LAG3 (CD223) is the third IR to be targeted in the clinic. It is a potential cancer immunotherapeutic target due to its negative regulatory role on T cells and its capacity, in combination with PD1, to mediate a state of exhaustion [PMID: 26018646]. LAG3 up-regulation is required to control overt activation and prevent the onset of autoimmunity. However, persistent antigen exposure in the tumor microenvironment results in sustained LAG3 expression, contributing to a state of exhaustion manifest in impaired proliferation and cytokine production. The exact signaling mechanisms downstream of LAG3 and interplay with other IRs remains largely unknown. However, the striking synergy between LAG3 and PD1 observed in multiple settings, coupled with the contrasting intracellular cytoplasmic domain of LAG3 as compared with other IRs, highlights the potential uniqueness of LAG3. There are now four LAG3-targeted therapies in the clinic with many more in preclinical development [PMID: 28258692].

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded human tonsil. Anti-LAG3 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
    • IHC shows positive staining in paraffin-embedded human Hodgkin's lymphoma. Anti-LAG3 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
    • IHC shows positive staining in paraffin-embedded human tonsil. Anti-LAG3 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
    • IHC shows positive staining in paraffin-embedded human bladder cancer. Anti-LAG3 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
    • IHC shows positive staining in paraffin-embedded human thyroid cancer. Anti-LAG3 antibody was used at 1/1000 dilution, followed by a HRP Polymer for Mouse & Rabbit IgG (ready to use). Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.
  • 免疫荧光

    • Flow cytometric analysis of Human CD326 expression on 4% PFA fixed 90% methanol permeabilized HeLa cells. Cells from the Hela (Human cervix adenocarcinoma epithelial cells) were stained with either Cy5 Rabbit IgG Isotype Control (Black line histogram) or SDT β-actin Recombinant Rabbit mAb (Cy5 Conjugate) (Red line histogram) at 0.1 μg/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

    • Flow cytometric analysis of Human CD326 expression on 4% PFA fixed 90% methanol permeabilized NIH/3T3 cells. Cells from the NIH/3T3 (Mouse embryonic fibroblast) were stained with either Cy5 Rabbit IgG Isotype Control (Black line histogram) or SDT β-actin Recombinant Rabbit mAb (Cy5 Conjugate) (Red line histogram) at 0.1 μg/test, cells without incubation with primary antibody and secondary antibody (Blue line histogram) was used as unlabelled control. Flow cytometry and data analysis were performed using BD FACSymphony™ A1 and FlowJo™ software.

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