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DF13997-200
a rare autosomal dominant disorder which predominantly affects noncornified stratified squamous epithelia and is characterized by the presence of soft
cytoplasmic is an enzyme that in humans is encoded by the GOT1 gene
BS2774-100
UNIProt ID: Q15149
KCTD16 Polyclonal Antibody - E-AB-52282 HeLa Transfection DF13997-200KCTD16 Polyclonal Antibody Sizes: 60L, 120L, 200L Catalogue Numbers: E AB 52282 60, E AB 52282 120, E AB 52282 200 Citations, Manuals and MSDS Available upon request. Abbreviation: KCTD16 Target Synonym: BTB POZ domain containing protein KCTD16; BTB POZ domain containing protein KCTD16; DKFZp781A1155; KCD16; KCTD16; KIAA1317; MGC138167; Potassium channel tetramerisation domain containing 16; Potassium channel tetramerization domain containing protein
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