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frontometaphyseal dysplasia (FMD)
Read-through transcription from the neighboring upstream gene (NME1) generates naturally-occurring transcripts (NME1-NME2) that encode a fusion protein comprised of sequence sharing identity with each individual gene product
which is required for ubiquitin-mediated degradation of cell cycle G1 regulators
Swissprot No Q8WUM4 Gene Accession NP_001155901 WB Predicted band size 96 kDa WB Positive control WB Recommended dilution 500-2000 IHC predicted cell location Predicted cell location: Cytoplasm IHC positive control Positive control: Human liver cancer IHC Recommed dilution Recommended dilution: 50-200 Storage
Cancer and Immunology Studies
MAP1LC3B rabbit monoclonal antibody package:50 μl frontometaphyseal dysplasia (FMD)Specification Full name MAP1LC3B rabbit monoclonal antibody Alternative names 50 l 100 l Reactivity rabbit monoclonal Applications WB Host Rabbit Clone type rabbit monoclonal Target Background The product of this gene is a subunit of neuronal microtubule associated MAP1A and MAP1B proteins, which are involved in microtubule assembly and important for neurogenesis. Studies on the rat homolog implicate a role for this gene in autophagy, a process that
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