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FIGURE: 1 / 3
Recommended positive controls: 293T, HeLa.
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
This gene encodes a member of the cytoskeletal BTB/kelch repeat family. The encoded protein plays a role in neurofilament architecture and is involved in mediating the ubiquitination and degradation of some proteins. Defects in this gene are a cause of giant axonal neuropathy.
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For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: asterless; CC-CKR-8; CCR-8; CDw198; centrosomal protein 152kDa; Centrosomal protein of 152 kDa; Cep152; CKRL1; CMKBR8; CMKBRL2; CY6; GPRCY6; microcephaly, primary autosomal recessive 4; TER1
Gene Aliases: AI851464; CEP152; KIAA0912; MCPH4; MCPH9; mKIAA0912; SCKL5
UniProt ID: (Human) O94986, (Mouse) A2AUM9
Entrez Gene ID: (Human) 22995, (Mouse) 99100
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