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Alexa Fluor® 647 Rat Anti-Mouse/Human CD324 Antibody (S-R650)

Cadherin-1,CAM 120/80,Epithelial cadherin (E-cadherin),Uvomorulin,CDHE,UVO,CDH1

价格 1,280.00 供应商现货 : 3-5个工作日
货号 S0B5191
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产品规格
  • 宿主来源

    Rat
  • 抗原名称

    CD324
  • 分子别名

    Cadherin-1; CAM 120/80; Epithelial cadherin (E-cadherin); Uvomorulin; CDHE; UVO; CDH1
  • 细胞定位

    Cell membrane, Cytoplasm, Endosome
  • Accession

    P12830
  • 克隆号

    S-R650
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG1,k
  • 反应种属 ?

    Ms
  • 阳性样本

    HT-29
  • 纯化方式

    Protein G
  • 浓度

    0.05mg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 1% BSA, 0.3% Proclin 300
  • 储存条件

    12 months from date of receipt / reconstitution, 2 to 8 °C as supplied.
  • 应用

    FCM

  • 稀释度

    应用 稀释度 推荐种属
    FCM 5μl per million cells in 100μl volume Hu, Ms
背景介绍
  • CD324, also known as E-cadherin or cadherin-1, is a calcium-dependent cell adhesion protein that plays a crucial role in maintaining epithelial tissue integrity and regulating cell proliferation, differentiation, and survival. It is a member of the cadherin superfamily and is widely expressed on the cell surface of most epithelial tissues. The extracellular domain of CD324 facilitates homophilic binding between adjacent cells, while its cytoplasmic domain interacts with the actin cytoskeleton through catenins. This protein is essential for epithelial cell cohesion and acts as an invasion suppressor, with its loss often indicating high tumor aggressiveness in cancer.

  • 流式分析

    • Flow cytometric analysis of CD324 expression on HT-29 cells. Cells from the HT-29 (Human colorectal adenocarcinoma epithelial cell, Right) or MDA-MB-231 (Human breast adenocarcinoma epithelial cell, Left) was stained with either Alexa Fluor® 647 Rat IgG1, κ Isotype Control (Black line histogram) or SDT Alexa Fluor® 647 Rat Anti-Mouse/Human CD324 Antibody (Red line histogram) at 5μl/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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