Mouse transmembrane and coiled-coil domains 1 ELISA Kit | TMCO1 elisa kit
Mouse Transmembrane and coiled-coil domain-containing protein 1, TMCO1 ELISA Kit
NCBI and Uniprot Product Information
Uniprot Description
TMCO1: Defects in TMCO1 are the cause of craniofacial dysmorphism skeletal anomalies and mental retardation syndrome (CFSMR). A disorder characterized by craniofacial and skeletal anomalies, associated with mental retardation. Typical craniofacial dysmorphism include brachycephaly, highly arched bushy eyebrows, synophrys, long eyelashes, low-set ears, microdontism of primary teeth, and generalized gingival hyperplasia, whereas Sprengel deformity of scapula, fusion of spine, rib abnormities, pectus excavatum, and pes planus represent skeletal anomalies. Belongs to the TMCO1 family. 2 isoforms of the human protein are produced by alternative splicing.
Protein type: Membrane protein, integral; Membrane protein, multi-pass
Cellular Component: Golgi apparatus; membrane; endoplasmic reticulum; integral to membrane
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Product Notes
The Mouse TMCO1 tmco1 (Catalog #AAA9331366) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA9331366 ELISA Kit recognizes Mouse TMCO1. It is sometimes possible for the material contained within the vial of "transmembrane and coiled-coil domains 1, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
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