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HDAC4 Polyclonal Antibody

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    HDAC4 Polyclonal Antibody
  • HDAC4 Polyclonal Antibody
Cat No: 13494
Polyclonal&monoclonal Antibody - Miscellaneous Antibodies
Cayman
€348.00
Price is excluding VAT and does not include packaging neither shipping

Antigen: synthetic peptide corresponding to amino acids 194-209 of human HDAC4 • Host: rabbit • Cross Reactivity:(+) human and mouse HDAC4 • Application(s): WB, IP, and ChIP • HDAC4 is a class II HDAC that can shuttle between the nucleus and cytoplas...

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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 Technologies only in Europe
Product Overview:
Antigen: synthetic peptide corresponding to amino acids 194-209 of human HDAC4 • Host: rabbit • Cross Reactivity:(+) human and mouse HDAC4 • Application(s): WB, IP, and ChIP • HDAC4 is a class II HDAC that can shuttle between the nucleus and cytoplasm, suggesting potential extranuclear functions by regulating the acetylation status of non-histone substrates.
Histone deacetylase (HDAC) and histone acetyltransferase (HAT) are enzymes that regulate transcription by selectively deacetylating or acetylating the ε-amino groups of lysines located near the amino termini of core histone proteins. Eleven members of HDAC family have been identified in the past several years. These HDAC family members are divided into two classes, I and II. HDAC4 is a member of the class II family which also includes HDACs 5, 6, and 7, the molecular weights of which are all about two-fold larger than those of the class I members.
Size: 1 ea
Shipping: wet ice
Stability: Store at -20 degrees; shelf life 365 days maximum after production
Host: rabbit
Antigen: synthetic peptide corresponding to amino acids 194-209 of human HDAC4
Application(s):

ChIP, IP, and WB

Formulation: 100 μg of Protein G purified IgG in 200 μl PBS containing 0.05% BSA and 0.05% 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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