Molecular Biology

E3 ubiquitin-protein ligase RNF31 (UniProt: Q96EP0 also known as EC: 2.3.

Specificity Recognizes Endonuclease G (EndoG), a mitochondrion-specific nuclease that translocates to the nucleus and cleaves chromatin DNA during apoptosis. EndoG is specifically activated by apoptotic stimuli and is able to induce nucleosomal

Fatty acid-binding protein 5 (FABP5) is also called Fatty acid-binding protein, epidermal, Epidermal-type fatty acid-binding protein (E-FABP), and Psoriasis-associated fatty acid-binding protein homolog (PA-FABP). FABP5 has a high specificity for

Free fatty acid receptor 2 (FFAR2), also known as G-protein coupled receptor 43 (GPR43), functions as the cell membrane receptor for short chain fatty acids that ultimately stimulates G protein coupled, inhibitory (Gi) signals via the adenylate

Forkhead box protein K2 (UniProt: Q01167 also known as Cellular transcription factor ILF-1, FOXK1, Interleukin enhancer-binding factor 1) is encoded by the FOXK2 (also known as ILF, ILF1) gene (Gene ID: 3607) in human. Forkhead box protein K2 is a

FOXK2 belongs to the mammalian forkhead transcription factor family and contains forkhead DNA-binding domain and an FHA domain at the N-terminal region. Immunogen Synthetic peptide directed towards the C terminal region of human FOXK2 Application

Immunogen Recombinant protein corresponding to GIPC PDZ domain containing family, member 1. Sequence MPLGLGRRKKAPPLVENEEAEPGRG Application All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas

Glial fibrillary acidic protein is a class-III intermediate filament. GFAP is the main constituent of intermediate filaments in astrocytes and serves as a cell specific marker that distinguishes differentiated astrocytes from other glial cells

Purified rat monoclonal antibody. Recognizes the ~55 kDa glial fibrillary acidic protein (GFAP).

Glucocerebrosidase is an enzyme having glucosylceramidase activity. Defect in lysosomal hydrolase glucocerebrosidase results in Gaucher disease.

Glucocerebrosidase is an enzyme having glucosylceramidase activity. Defect in lysosomal hydrolase glucocerebrosidase results in Gaucher disease.

Specificity Recognizes Glutamate Receptor 1 [GluR1], phosphoSer831. The antibody recognizes a protein of ~100 kDa corresponding to GluR1 phosphorylated at Ser831 in rat hippocampal homogenate.