您现在的位置: 首页   -  产品中心   -  免疫学   -   抗体
CEA(CD66e) Recombinant Rabbit mAb (SDT-098-54)

CEA(CD66e) Recombinant Rabbit mAb (SDT-098-54)

货号: S0B2091
价格: 600
规格: 25μl
介绍: -
其他: -
产品规格
  • 宿主来源

    Rabbit
  • 抗原名称

    CEA
  • 分子别名

    Carcinoembryonic antigen-related cell adhesion molecule 5, Carcinoembryonic antigen, CD66e
  • 免疫原

    Recombinant Protein
  • 细胞定位

    Cell membrane
  • Accession

    P06731
  • 克隆号

    SDT-098-54
  • 抗体类型

    Rabbit mAb
  • 应用

    IHC-P, ICC, WB, IP, IF
  • 反应种属 ?

    Hu
  • 纯化方式

    Protein A
  • 浓度

    0.25 mg/ml
  • 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
ICC 1:50
IHC-P 1:1000
WB 1:500-10000
IP 1:25
IF 1:500
背景介绍
  • Carcinoembryonic antigen (CEA) describes a set of highly related glycoproteins involved in cell adhesion. CEA is normally produced in gastrointestinal tissue during fetal development, but the production stops before birth. CEA are glycosyl phosphatidyl inositol (GPI) cell-surface-anchored glycoproteins whose specialized sialofucosylated glycoforms serve as functional colon carcinoma L-selectin and E-selectin ligands, which may be critical to the metastatic dissemination of colon carcinoma cells. Immunologically they are characterized as members of the CD66 cluster of differentiation. The proteins include CD66a, CD66b, CD66c, CD66d, CD66e, CD66f.Consequently, CEA is usually present at very low levels in the blood of healthy adults (about 2–4 ng/mL). However, the serum levels are raised in some types of cancer. CEA is an important tumor marker for colorectal and some other carcinomas. The CEA subgroup members are cell membrane associated and show a complex expression pattern in normal and cancerous tissues with notably CEA showing a selective epithelial expression.

  • 免疫印迹

    • WB result of CEA Rabbit mAb                             

      Primary antibody: CEA Rabbit mAb at 1/500 dilution
      Lane 1: PANC-1 whole cell lysate 20 µg
      Lane 2: MCF7 whole cell lysate 20 µg
      Lane 3: HT-29 whole cell lysate 20 µg
      Negative control: PANC-1 whole cell lysate   

      Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 200~250 kDa
      Observed MW: 200~250 kDa
      Exposure time: 180s

    • WB result of CEA Rabbit mAb                             

      Primary antibody: CEA Rabbit mAb at 1/10000 dilution
      Lane 1: BxPC-3 whole cell lysate 20 µg

      Secondary antibody: Goat Anti-Rabbit IgG, (H+L), HRP conjugated at 1/10000 dilution
      Predicted MW: 200~250 kDa
      Observed MW: 250 kDa
      Exposure time: 30s

  • 免疫沉淀

    • CEA Rabbit mAb at 1/25 dilution (1µg) immunoprecipitating CEA in 0.4mg MCF7 whole cell lysate.
      Western blot was performed on the immunoprecipitate using CEA Rabbit mAb at 1/1000 dilution.
      Secondary antibody (HRP) for IP was used at 1/400 dilution.
      Lane 1 : MCF7 whole cell lysate 30µg(input)
      Lane 2 : CEA Rabbit mAb IP in MCF7 whole cell lysate
      Lane 3 : Rabbit monoclonal IgG IP in MCF7 whole cell lysate
      Predicted MW: 200~250 kDa
      Observed MW: 230 kDa
      Exposure time: 60s

  • 免疫组化

    • IHC shows positive staining in paraffin-embedded human colon. Anti-CEA(CD66e) antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) 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 colon cancer. Anti-CEA(CD66e) antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) 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 lung adenocarcinoma. Anti-CEA(CD66e) antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) 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 medullary thyroid carcinoma. Anti-CEA(CD66e) antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) 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 negative staining in paraffin-embedded human papillary thyroid carcinoma. Anti-CEA(CD66e) antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) 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 breast cancer. Anti-CEA(CD66e) antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) 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 colon cancer. Anti-CEA(CD66e) antibody was used at 1/1000 dilution, followed by a Goat Anti-Rabbit IgG H&L (HRP) ready to use. Counterstained with hematoxylin. Heat mediated antigen retrieval with Tris/EDTA buffer pH9.0 was performed before commencing with IHC staining protocol.

  • 免疫细胞化学

    • ICC shows positive cell membrane staining in MCF7 cells. Anti-CEA(CD66e) antibody was used at 1/50 dilution 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.

    • Negative control: ICC shows negative staining in PANC-1 cells. Anti-CEA(CD66e) antibody was used at 1/50 dilution 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.

  • 免疫荧光

    • IF shows positive staining in paraffin-embedded human gastric carcinoma. Anti-CEA(CD66e) antibody was used at 1/500 dilution (magenta) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 647) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • IF shows positive staining in paraffin-embedded human cervical squamous cell carcinoma. Anti-CEA(CD66e) antibody was used at 1/500 dilution (magenta) and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 647) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.

    • Negative control: IF shows negative staining in paraffin-embedded human papillary thyroid carcinoma. Anti-CEA(CD66e) antibody was used at 1/500 dilution and incubated overnight at 4°C. Goat polyclonal Antibody to Rabbit IgG - H&L (Alexa Fluor® 647) was used as secondary antibody at 1/1000 dilution. Counterstained with DAPI (Blue). Heat mediated antigen retrieval with EDTA buffer pH9.0 was performed before commencing with IF staining protocol.