Anti-Mouse CD90 (Thy-1) (Clone HK2.1) – Purified in vivo PLATINUM™ Functional Grade
Anti-Mouse CD90 (Thy-1) (Clone HK2.1) – Purified in vivo PLATINUM™ Functional Grade
Product No.: C635
Clone HK2.1 Target CD90 Formats AvailableView All Product Type Monoclonal Antibody Alternate Names T25, CD90, Thy-1, Thy1.1, Thy1.2, Thy-1.2 Isotype Rat IgG2c Applications FA , in vivo , WB |
Antibody DetailsProduct DetailsReactive Species Mouse Host Species Rat Recommended Isotype Controls Rat IgG2c Recommended Dilution Buffer Product Concentration ≥ 5.0 mg/ml Endotoxin Level <0.5 EU/mg as determined by the LAL method Purity ≥98% 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. Pathogen Testing To protect mouse colonies from infection by pathogens and to assure that experimental preclinical data is not affected by such pathogens, all of Leinco’s Purified Functional PLATINUM™ antibodies are tested and guaranteed to be negative for all pathogens in the IDEXX IMPACT I Mouse Profile. 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_2829791 Applications and Recommended Usage? Quality Tested by Leinco FC FC The suggested concentration for this HK2.1 antibody for staining cells in flow cytometry is ≤ .25 μg per 106 cells in a volume of 100 μl or 100μl of whole blood. Titration of the reagent is recommended for optimal performance for each application. 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 HK2.1 recognizes a non-polymorphic determinant on mouse CD90 (Thy1.1 and Thy1.2 alloantigens). Background CD90 is a 28-30 kD GPI-linked membrane glycoprotein and is part of the Ig superfamily. It interacts with CD45 in signal transduction. CD90 mediates adhesion of thymocytes to thymic stroma. It has been reported that CD90 binds with β2 and β3 integrins and is involved in the inhibition of hematopoietic stem cells proliferation and differentiation, as well as the regulation of cell adhesion and neurite outgrowth. It can be used as a marker for various stem cells, such as hematopoietic stem cells, and for the axonal processes of mature neurons. For use in FACS, CD90 is a popular surface marker for stem cells in combination with other markers such as CD34. There are two alleles for CD90 in mice that differ by one amino acid. The difference being that CD90.1 (Thy1.1) has an arginine and CD90.2 (Thy1.2) has a glutamine at position 108. CD90.2 is more prevalent and is expressed in most mice strains. CD90.1 is only expressed by a select few mice strains including AKR/J and PL strains. CD90.2 is a 25-35 kD GPI-anchored membrane glycoprotein. Like CD90, it is also in the Ig superfamily, interacts with CD45, and has involvement in signal transduction. The function of CD90.2 is thought to play roles in cognition, axon growth, T lymphocyte function, and apoptosis. CD90 acts as tumor suppressor for some tumors due to its action in upregulating thrombospondin, SPARC (osteonectin), and fibronectin. On the other hand, it has been suspected to aid in the spread of circulating melanoma cells. Regarding prostate cancer, CD90 has therapeutic potential for specific drug targeting due to its expression in cancer associated stroma, but not in normal stroma. Antigen Distribution CD90 is expressed by thymocytes, peripheral T cells, myoblasts, epidermal cells, and keratinocytes. PubMed NCBI Gene Bank ID UniProt.org Research Area Immunology . Stem Cell 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 clone HK2.1 is a monoclonal antibody used in in vivo mouse studies to target and recognize CD90 (Thy-1) alloantigens, specifically both Thy-1.1 and Thy-1.2, which are present on most mouse strains. Key uses and features in in vivo mouse studies:
Modes of application:
Summary Table: Clone HK2.1 in In Vivo Mouse Studies
No direct information was found in the results about specific disease models or exact dosing protocols; these are usually defined by the experimental design and available from manufacturers or in primary literature for each indicated use. The antibodys broad specificity and low endotoxin content make it suitable for a variety of applications in mouse immunology and stem cell research. For sterile packaged clone HK2.1 (a cell linelikely derived from the proximal tubule HK2common in cell biology research), the correct storage temperature is below -130°C, preferably in the vapor phase of liquid nitrogen, until ready for use. This is the standard for long-term cryopreservation of most cultured mammalian cells and is recommended to maintain maximum cell viability. Key points:
Do not store cells at temperatures above -80°C for extended periods, as this will significantly reduce viability and may result in loss of the clone. For immediate use, follow the established thawing and culturing protocols. Summary Table
Conclusion: Commonly used antibodies or proteins with HK2.1 in the literature include a variety of metabolic enzymes, stem cell markers, and housekeeping proteins for controls. The following are among the most frequently co-used antibodies and proteins in studies with HK2:
These proteins are chosen because they represent controls, markers of cell state (such as stemness or metabolic activity), or are mechanistically linked to HK2s role in cellular metabolism and cancer biology. Researchers commonly use these antibodies in western blot and immunofluorescence to study HK2 interactions, localization, and expression profile. Additionally, HK1 is often studied alongside HK2 to distinguish isoform-specific effects in metabolic studies or genetic models. When tags or genetic manipulations are employed, HA, Flag, or GST tag antibodies are used for detection of exogenously expressed or purified proteins. Experimental controls in these setups regularly include antibodies against tubulin and GAPDH to verify equal protein loading on gels or in immunostaining experiments. This reflects a broad approach in literature, where the study of HK2.1 typically intersects with cell metabolism, stemness, and cellular stress proteins. The key findings from citations mentioning clone HK2.1 in scientific literature are not directly available in the provided search results. There are no references to a "clone HK2.1" as a scientific reagent, cell line, or antibody in the cited articles. Instead, the results address topics related to the enzyme hexokinase II (HK2) and the protein human Kallikrein 2 (hK2), but without explicit mention of a "clone HK2.1." Essential context:
Additional information:
If your query pertains to a specific scientific reagent (antibody, cell line, etc.), more precise detailssuch as its catalog number, application, or targeted moleculeare needed to locate relevant scientific citations. If further clarification or context is provided, more targeted findings can be synthesized. References & Citations1. Ledbetter, J. A. et al. (1979) Immunol. Rev. 47:63
2. Ledbetter, J. A. et al. (1980) J. Exp. Med. 152:280
3. Lancki, D. W. et al. (1984) Immunol. Rev. 81:65 Technical ProtocolsCertificate of Analysis |
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