Anti-Human CD71 (Clone T56/14) – Purified in vivo GOLD™ Functional Grade
Anti-Human CD71 (Clone T56/14) – Purified in vivo GOLD™ Functional Grade
Product No.: C371
Clone T56/14 Target CD71 Formats AvailableView All Product Type Monoclonal Antibody Alternate Names Transferrin Receptor Isotype Mouse IgG1 Applications FC , IHC , IP |
Antibody DetailsProduct DetailsReactive Species Human Host Species Mouse Recommended Isotype Controls Recommended Isotype Controls Recommended Dilution Buffer Product Concentration ≥ 5.0 mg/ml Endotoxin Level < 1.0 EU/mg as determined by the LAL method Purity ≥95% monomer by analytical SEC ⋅ >95% by SDS Page Formulation This monoclonal antibody is aseptically packaged and formulated in 0.01 M phosphate buffered saline (150 mM NaCl) PBS pH 7.2 - 7.4 with no carrier protein, potassium, calcium or preservatives added. Due to inherent biochemical properties of antibodies, certain products may be prone to precipitation over time. Precipitation may be removed by aseptic centrifugation and/or filtration. Product Preparation Functional grade preclinical antibodies are manufactured in an animal free facility using in vitro cell culture techniques and are purified by a multi-step process including the use of protein A or G to assure extremely low levels of endotoxins, leachable protein A or aggregates. Storage and Handling Functional grade preclinical antibodies may be stored sterile as received at 2-8°C for up to one month. For longer term storage, aseptically aliquot in working volumes without diluting and store at ≤ -70°C. Avoid Repeated Freeze Thaw Cycles. Country of Origin USA Shipping Next Day 2-8°C RRIDAB_2829683 Each investigator should determine their own optimal working dilution for specific applications. See directions on lot specific datasheets, as information may periodically change. DescriptionDescriptionSpecificity Clone T56/14 recognizes human CD71. Background CD71 is a 95 kD type II homodimeric transmembrane glycoprotein. The function of CD71 is believed to be primarily nutritional. It plays a role in the control of cellular proliferation through facilitation of iron uptake by way of ferrotransferrin binding and the recycling of apotransferrin to the cell surface. Additionally, transferrin receptor is required for erythropoiesis and proper neurological development, and it has also been suggested that a growth signal might be generated by the transferrin/transferrin receptor interaction. Current genetic analysis indicates that the structural genes for transferrin receptor and for a melanoma-associated antigen (p97), and perhaps transferrin itself, each map to a common chromosome in humans. These proteins exhibit primary sequence homology with transferrin and have the ability to bind ferric iron. Therefore, it is thought that genetic rearrangements in this iron transport region may be associated with malignant transformation. Hence, anti-CD71 mAbs are thought to have therapeutic potential in cases of human leukemia & lymphoma. Antigen Distribution CD71 is expressed on most proliferating cells, activated lymphocytes, monocytes, macrophages, erythroid progenitors, and brain endothelium. Ligand/Receptor Transferrin PubMed NCBI Gene Bank ID UniProt.org Research Area Immunology Leinco Antibody AdvisorPowered by AI: AI is experimental and still learning how to provide the best assistance. It may occasionally generate incorrect or incomplete responses. Please do not rely solely on its recommendations when making purchasing decisions or designing experiments. The T56/14 clone is a monoclonal antibody that reacts with human CD71 (also known as transferrin receptor or TfR1) and is specifically designed for in vivo research applications in mouse studies. Primary Applications in Mouse StudiesThe T56/14 antibody is commonly used in xenograft tumor models where human cancer cells are implanted into immunocompromised mice. Since this antibody specifically targets human CD71, it allows researchers to study human tumor cells within a mouse host without cross-reacting with mouse tissues. Mechanism and TargetCD71 is a type II homodimeric transmembrane glycoprotein expressed on proliferating cells, reticulocytes, and erythroid precursors. It plays a crucial role in cellular proliferation and iron import from transferrin into cells. The protein is particularly relevant for cancer research because it's expressed at high levels on malignant cells, and its expression correlates with cancer progression. Antibody Characteristics for In Vivo UseThe T56/14 antibody has several important characteristics that make it suitable for in vivo mouse studies:
Research ApplicationsBeyond basic xenograft studies, the T56/14 clone is used in various in vivo research contexts including flow cytometry and immunoprecipitation studies of tumor samples extracted from treated mice. This allows researchers to analyze CD71 expression levels and distribution in tumor tissues after various experimental treatments. The antibody is particularly valuable for studying cancer progression, cellular proliferation mechanisms, and iron metabolism in human tumor models established in mice, providing insights into how these processes might be targeted therapeutically. The T56/14 antibody is most commonly used to detect human CD71 (transferrin receptor, also known as TFRC) in various immunological assays such as flow cytometry, immunoprecipitation, and western blotting. In the scientific literature, researchers frequently use T56/14 in combination with several other antibodies or markers, depending on the experimental goal:
These combinations are guided by the biology of CD71, which is highly expressed on proliferating and activated cells, as well as on erythroid precursors. Other proteins or antibodies that are less directly related but sometimes assessed in tandem with CD71 (T56/14) in broader panels include:
Summary of common combinations with T56/14:
The exact combination depends on the experimental design, focus, and cell types under investigation. Specific literature examples will list unique panels, but these markers are consistent with the biology of CD71 and its applications. There are no directly relevant or widely cited key findings in scientific literature specifically associated with "clone T56/14." None of the major search results indicate recognition or discussion of a "clone T56/14" antibody, cell line, or genetic construct in well-known journals or databases. The search results reference the following, which do not relate directly to "clone T56/14":
If your query refers to an antibody (often called "clone X"), a transgenic line, or a plasmid referenced as T56/14, there is no evidence from authoritative literature that it is widely cited or recognized in the current scientific record. Alternative explanations for your query could include a typographical error in the clone name, or a reference to a reagent of very limited or niche use. If clarification or a corrected clone reference can be provided, a more targeted literature search can be performed. Dosing regimens for clone T56/14 are not explicitly detailed in the available search results, and there is no direct reference to this clone in the context of mouse models or antibody dosing guidelines provided. As such, I cannot provide authoritative dosing schedules or variations specific to clone T56/14 across differing mouse models based solely on the retrieved documents. If clone T56/14 refers to an antibody (common with the T numbering), standard practice for monoclonal antibodies in vivo involves the following considerations (based on general antibody dosing guides for mice):
Without more direct data on clone T56/14:
Key Limitations:
If you have more information on what clone T56/14 targets or its application area, I can offer more tailored protocol guidance using general principles from antibody dosing in mouse models. For now, dosing strategies would follow standard monoclonal antibody protocols as outlined above. References & Citations1. Pessin, JE. et al. (2003) J Biol Chem. 278(12):10683-90. Article Link 2. Trowbridge, SI. et al. (1981) Proc. Nat'l. Acad. Sci. 78:3039 3. Iacopetta, BJ. et al. (1983) J. Histochem. Cytochem. 31:336 Technical ProtocolsCertificate of Analysis |
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