Cat. #151120
Anti-Plasma Cell [LIV3G11]
Cat. #: 151120
Sub-type: Primary antibody
Unit size: 100 ug
Availability: 3-4 weeks
Target: Plasma cells (human, cytoplasmic).
Class: Monoclonal
Application: IHC
Reactivity: Human
Host: Mouse
£300.00
This fee is applicable only for non-profit organisations. If you are a for-profit organisation or a researcher working on commercially-sponsored academic research, you will need to contact our licensing team for a commercial use license.
Contributor
Inventor: J. Rhodes
Institute: University of Liverpool
Tool Details
*FOR RESEARCH USE ONLY (for other uses, please contact the licensing team)
- Name: Anti-Plasma Cell [LIV3G11]
- Research fields: Cell biology;Immunology
- Clone: LIV3G11
- Tool sub type: Primary antibody
- Class: Monoclonal
- Conjugation: Unconjugated
- Reactivity: Human
- Host: Mouse
- Application: IHC
- 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.
- Immunogen: Pancreatic cancer related serum mucin
- Isotype: IgG2a
- Recommended controls: Tonsil or lymph node
Target Details
- Target: Plasma cells (human, cytoplasmic).
- Tissue cell line specificity: Tonsil or lymph node
- Target background: Plasma cells are antibody secreting cells found in the lymphoid tissue and derived from B cells.
Applications
- Application: IHC
Handling
- Format: Liquid
- Concentration: 0.9-1.1 mg/ml
- Unit size: 100 ug
- Storage buffer: PBS with 0.02% azide
- Storage conditions: -15° C to -25° C
- Shipping conditions: Shipping at 4° C
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.
