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CD37 Monoclonal Antibody (Clone IPO-24)

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Cat No: 10004718
Polyclonal&monoclonal Antibody - Miscellaneous Antibodies
Cayman
€256.00
Price is excluding VAT and does not include packaging neither shipping

Host: mouse, clone IPO-24 · Cross Reactivity: (+) human CD37 · Application(s): (+) FC, ICC, and IHC (formalin-fixed paraffin-embedded tissue and frozen sections); (−) WB
CD37 is a type III transmembrane glycoprotein (Mr = 40-52 kDa). The leukocyte-sp...

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: 1 ea

This product can only be bought through Cayman Chemical. Please contact us.

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Territorial Availability: Available through Bertin Pharma only in Europe
Product Overview:
Host: mouse, clone IPO-24 · Cross Reactivity: (+) human CD37 · Application(s): (+) FC, ICC, and IHC (formalin-fixed paraffin-embedded tissue and frozen sections); (−) WB
CD37 is a type III transmembrane glycoprotein (Mr = 40-52 kDa). The leukocyte-specific protein CD37 is a member of the tetraspanin superfamily, originally described as a cell surface glycoprotein expressed on mature human B cells, but not on pro-B cells or plasma cells. T cells and monocytes express CD37 at low levels. In humans, CD37 expression is restricted to B and T lymphocytes, monocytes, macrophages, neutrophils, dendritic cells, and certain leukocyte-derived malignant cells. CD37 is not expressed by NK cells, platelets, or erythrocytes. CD37 monoclonal antibody is recommended for immunophenotyping of B cell neoplasia (B cell chronic lymphocytic leukemia, hairy cell leukemia, and B cell non-Hodgkin’s lymphomas). Human, rat, and murine CD37 sequences have been identified.
Size: 1 ea
Shipping: wet ice
Stability: Store at 4 degrees; shelf life 365 days maximum after production
Host: mouse
Clone: IPO-24
Application(s):

(+) FC, ICC, and IHC (formalin-fixed paraffin-embedded tissue and frozen sections); (−) WB

Specificity:
Formulation: 100 µg of affinity-purified IgG2b in 500 µl PBS, pH 7.2, containing 0.02% sodium azide
Custom Code: 3822000002
UNSPSC code: 12352203

Cayman Chemical's mission is to help make research possible by supplying scientists worldwide with the basic research tools necessary for advancing human and animal health. Our utmost commitment to healthcare researchers is to offer the highest quality products with an affordable pricing policy.

Our scientists are experts in the synthesis, purification, and characterization of biochemicals ranging from small drug-like heterocycles to complex biolipids, fatty acids, and many others. We are also highly skilled in all aspects of assay and antibody development, protein expression, crystallization, and structure determination.

Over the past thirty years, Cayman developed a deep knowledge base in lipid biochemistry, including research involving the arachidonic acid cascade, inositol phosphates, and cannabinoids. This knowledge enabled the production of reagents of exceptional quality for cancer, oxidative injury, epigenetics, neuroscience, inflammation, metabolism, and many additional lines of research.

Our organic and analytical chemists specialize in the rapid development of manufacturing processes and analytical methods to carry out clinical and commercial GMP-API production. Pre-clinical drug discovery efforts are currently underway in the areas of bone restoration and repair, muscular dystrophy, oncology, and inflammation. A separate group of Ph.D.-level scientists are dedicated to offering Hit-to-Lead Discovery and Profiling Services for epigenetic targets. Our knowledgeable chemists can be contracted to perform complete sample analysis for analytes measured by the majority of our assays. We also offer a wide range of analytical services using LC-MS/MS, HPLC, GC, and many other techniques.

Accreditations
ISO/IEC 17025:2005
ISO Guide 34:2009

Cayman is a leader in the field of emerging drugs of abuse, providing high-purity Schedule I-V Controlled Substances to federally-licensed laboratories and qualified academic research institutions for forensic analyses. We are certified by ACLASS Accreditation Services with dual accreditation to ISO/IEC 17025:2005 and ISO Guide 34:2009.

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