您现在的位置: 首页   -  产品中心   -  免疫学   -   抗体
Alexa Fluor® 647 Rat Anti-Mouse/Human CD324 Antibody (S-R650)

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

货号: S0B5191
价格: 560
规格: 20T
介绍: -
其他: -
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

    Endosome, Cell membrane, Cytoplasm
  • Accession

    P12830
  • 克隆号

    S-R650
  • 抗体类型

    Rat mAb
  • 抗体同种型

    IgG1,k
  • 应用

    FCM
  • 反应种属 ?

    Ms
  • 阳性样本

    HT-29
  • 纯化方式

    Protein G
  • 浓度

    50 μg/ml
  • 标记

    Alexa Fluor® 647
  • 性状

    Liquid
  • 缓冲体系

    PBS, 25% Glycerol, 1% BSA, 0.3% Proclin 300

  • 储存条件

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