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| Catalog Number | orb1906394 |
|---|---|
| Category | Antibodies |
| Description | Anti-EGFRvIII [806] |
| Target | EGFRvIII |
| Clonality | Monoclonal |
| Species/Host | Mouse |
| Isotype | IgG2b |
| Conjugation | Unconjugated |
| Reactivity | Human |
| Concentration | 1 mg/ml |
| Buffer/Preservatives | PBS with 0.02% Proclin 300. |
| Immunogen | The original antibody was generated by immunization of mice with NR6 mouse fibroblasts expressing the truncated de2–7 EGFR. |
| UniProt ID | P00533 |
| Tested applications | FC, IHC, IP |
| Clone Number | 806 |
| Storage | Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles. |
| Alternative names | de2–7 EGFR; EGF receptor; delta2–7 epidermal growt Read more... |
| Research Area | Cancer Biology |
| Note | For research use only |
| Expiration Date | 12 months from date of receipt. |
![Anti-EGFRvIII [806]](/images/pub/media/catalog/product/NewWebsite/35/orb1906394_1.png)
Immunofluorescence staining of A431 cells with anti-EGFRvIII antibody 806. Immunofluorescence analysis of paraformaldehyde fixed A431 cells on Shi-fix™ coverslips stained with the chimeric rabbit IgG version of 806 (orb1906395) (1:100 dilution) for 1h followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing cell junction staining. The nuclear stain is DAPI (blue). Panels show, from left-right, top-bottom, orb1906395, DAPI, merged channels, and an isotype control. The isotype control was an unknown specificity antibody (orb256458) followed by staining with Alexa Fluor® 488 secondary antibody.
![Anti-EGFRvIII [806]](/images/pub/media/catalog/product/NewWebsite/35/orb1906394_2.png)
Western blot using anti-EGFRvIII antibody 806. A431 (A) (0.003 µg/ml), HeLa (B) (0.3 µg/ml), and MDA-MB-231 (C) (0.1 µg/ml) cells lysates (35 µg protein in RIPA buffer) were resolved via SDS-PAGE, and the subsequent blots were probed with the chimeric rabbit version of 806 (orb1906395) at the mentioned respective concentrations before detection using an anti-rabbit secondary antibody. A primary incubation of 1 hour was used, and proteins were detected by chemiluminescence.
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