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P62/SQSTM1 Polyclonal Antibody - E-AB-70325 BioWorld Mutations in this gene are

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Description

Mutations in this gene are a cause of platelet-type bleeding disorder-11 (BDPLT11)

BS67516-100

The encoded protein differs from other NimA family members in that it is not cell cycle regulated and is found primarily in the cytoplasm

Some of these peptides are secreted and can bind to the acetyltransferase complex APBB1/TIP60 to promote transcriptional activation

Immunogen: A synthesized peptide derived from human NAA25

P62/SQSTM1 Polyclonal Antibody - E-AB-70325 BioWorld Mutations in this gene areP62 SQSTM1 Polyclonal Antibody Sizes: 60L, 120L, 200L Catalogue Numbers: E AB 70325 60, E AB 70325 120, E AB 70325 200 Citations, Manuals and MSDS Available upon request. Abbreviation: P62 SQSTM1 Target Synonym: A170; DMRV; EBI 3 associated protein of 60 kDa; EBI 3 associated protein p60; EBI3 associated protein of 60 kDa; EBI3 associated protein p60; EBI3 associated protein of 60 kDa; EBIAP; FTDALS3; MGC127197; ORCA; OSF 6; Osi; OSIL; Oxidative

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