| Product Type: | Rabbit polyclonal IgG, primary antibodies |
|---|---|
| Species reactivity: | Human, Mouse |
| Applications: | WB, FC |
| Clonality: | Polyclonal |
| Form: | Liquid |
| Storage condition: | Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term. |
| Storage buffer: | 1*PBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
| Concentration: | 1ug/ul |
| Purification: | Immunogen affinity purified. |
| Molecular weight: | Predicted band size 28 kDa |
| Isotype: | IgG |
| Immunogen: | Synthetic peptide within human Claudin18 aa 28-80. |
| Positive control: | Human stomach tissue lysate, AGS cell lysate, AGS, F9. |
| Subcellular location: | Cell membrane. |
| Recommended Dilutions:
WB FC |
1:500-1:1,000 1:500-1:1,000 |
| Uniprot #: | SwissProt: P56856 Human | P56857 Mouse |
| Alternative names: | Claudin 18 Claudin-18 CLD18_HUMAN CLDN18 SFTA5 SFTPJ |
|
Fig1:
Western blot analysis of Claudin 18.1 on different lysates. Proteins were transferred to a PVDF membrane and blocked with 5% BSA in PBS for 1 hour at room temperature. The primary antibody (ER1902-11, 1/500) was used in 5% BSA at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:5,000 dilution was used for 1 hour at room temperature. Positive control: Lane 1: human stomach tissue lysate Lane 2: AGS cell lysate |
|
Fig2:
Flow cytometric analysis of AGS cells labeling Claudin 18.1. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (ER1902-11, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |
|
Fig3:
Flow cytometric analysis of F9 cells labeling Claudin 18.1. Cells were washed twice with cold PBS and resuspend. Then stained with the primary antibody (ER1902-11, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black). |