flow cytometry: 2-5 μg/test using using Jurkat cells. immunoblotting: 5-10 μg/mL using using HepG2 total cell extracts. immunofluorescence: 5-10 μg/mL using using HepG2 cells.
Monoclonal Anti-FTL (mouse IgG1 isotype) is derived from the hybridoma FTL1.1 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a synthetic peptide corresponding to an internal sequence of human FTL. Ferritin, a highly conserved iron-binding protein, is composed of two subunits, namely a 21 kDa heavy (H) chain and a 19 kDa light (L) chain. Ferritin light chain (FTL) is encoded by the gene mapped to human chromosome 19q13.33. FTL is highly found in liver and spleen.
Specificity
Monoclonal Anti-FTL recognizes human FTL.
Immunogen
synthetic peptide corresponding to an internal sequence of human FTL.
Application
Monoclonal Anti-FTL antibody from mouse may be used in:
immunoblotting
flow cytometry
immunocytochemistry
Biochem/physiol Actions
Ferritin plays a vital role in maintaining iron homeostasis. The light chain ferritin, specifically mediates storage of iron in cells. Increased levels of FTL might lead to development of coronary artery disease (CAD) by regulating lipid oxidation within the vessel wall through reactive oxygen species generation. Furthermore, Mutation in the FTL gene causes an autosomal dominant, adult onset degenerative disease such as hereditary ferritinopathy (HF) or neuroferritinopathy. Interestingly, FTL has also been suggested as a tumor-associated macrophages related biomarker which is being utilized in prognosis prediction of breast cancer.
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
Storage and Stability
For extended storage, freeze at -20 °C in working aliquots. Repeated freezing and thawing,or storage in “frost-free” freezers,is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.
Disclaimer
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
Breast cancer development largely depends upon the essential contributions from the tumor microenvironment, where several inflammatory cell populations (e.g. macrophages) orchestrate breast cancer development. The majority of tumor-associated macrophages (TAMs) exhibit alternatively activated M2 properties, produce abundant anti-inflammatory factors and
Proteomic approach to coronary atherosclerosis shows ferritin light chain as a significant marker: evidence consistent with iron hypothesis in atherosclerosis
You SA, et al.
Physiological Genomics, 13(1), 25-30 (2003)
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