Enables separation from T and B cells.
| Inventor | Institute |
|---|---|
| John Horton | University of Durham |
| Cat. #: | 157743 |
|---|---|
| Tool sub type: | Primary antibody |
| Unit size: | 100 ug |
| Research Fields: | Cancer;Cell biology;Immunology |
| Application: | FACS ; IHC |
| Target: | Xenopus Natural Killer (NK) cells |
| Reactivity: | Xenopus laevis |
| Host: | Mouse |
| Class: | Monoclonal |
| Product description: | Enables identification of specific lymphoid populations in Xenopus (tested in liver, spleen and gut), namely NK cells. Enables separation from T and B cells. |
|---|---|
| Conjugation: | Unconjugated |
| Molecular weight: | 72 kDa |
| Immunogen: | Mice were immunised with splenocytes from early-thymectomized (Tx) Xenopus following B cell and thrombocyte depletion, therefore an enriched Natural Killer (NK) cell population. |
| Immunogen Uniprot ID: | Not applicable |
| Myeloma used: | P3X63Ag8.653 |
| Target background: | Enables identification of specific lymphoid populations in Xenopus (tested in liver, spleen and gut), namely NK cells. Enables separation from T and B cells. |
|---|
| Format: | Liquid |
|---|---|
| Concentration: | 0.9-1.1 mg/ml |
| Storage buffer: | PBS with 0.02% azide |
| Storage conditions: | -15° C to -25° C |
| Shipping conditions: | Dry ice |
| References: |
Horton et al. 2000. Eur J Immunol. 30(2):604-13. PMID: 10671217. |
|---|
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