LIV 3G11 reacts with normal and malignant plasma cells but not with normal B cells. The antigen shows a very high degree of specificity for plasma cells and LIV3G11 may be used to identifiy plasma cells in formalin- fixed tissue sections.
| Inventor | Institute |
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| J. Rhodes | University of Liverpool |
| SKU: | 151120 |
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| Product description: | LIV 3G11 reacts with normal and malignant plasma cells but not with normal B cells. The antigen shows a very high degree of specificity for plasma cells and LIV3G11 may be used to identifiy plasma cells in formalin- fixed tissue sections. |
| Conjugation: | Unconjugated |
| Isotype: | IgG2a |
| Immunogen: | Pancreatic cancer related serum mucin |
| Cat. #: | 151120 |
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| Provenance and Ownership: | The Anti-Plasma Cell [LIV3G11] is owned by Cancer Research UK. CancerTools supplies the Anti-Plasma Cell [LIV3G11] under licence from Cancer Research UK and is the authorised source for its distribution. Sourcing Anti-Plasma Cell [LIV3G11] directly from the IP owner ensures authenticity, provenance and compliance with all applicable licensing and research use requirements. |
| Tool sub type: | Primary antibody |
| Unit size: | 100 ug |
| Research Fields: | Cell biology; Immunology |
| Application: | IHC |
| Target: | Plasma cells (human, cytoplasmic). |
| Reactivity: | Human |
| Clone: | LIV3G11 |
| Host: | Mouse |
| Class: | Monoclonal |
| Target background: | Plasma cells are antibody secreting cells found in the lymphoid tissue and derived from B cells. |
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| Format: | Liquid |
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| 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: |
Ching et al. 1990. Int J Cancer. 45(6):1022-7. PMID: 2351483. Purification and characterization of a peanut-agglutinin-binding pancreatic-cancer-related serum mucus glycoprotein. Ching et al. 1988. Gastroenterology. 95(1):137-42. PMID: 3163659. Identification and partial characterization of a new pancreatic cancer-related serum glycoprotein by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and lectin blotting. |
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