TTDN1 Blocking Peptide | MPLKIP blocking peptide
TTDN1 Antibody (C-term) Blocking Peptide
NCBI and Uniprot Product Information
NCBI Description
The protein encoded by this gene localizes to the centrosome during mitosis and to the midbody during cytokinesis. The protein is phosphorylated by cyclin-dependent kinase 1 during mitosis and subsequently interacts with polo-like kinase 1. The protein is thought to function in regulating mitosis and cytokinesis. Mutations in this gene result in nonphotosensitive trichothiodystrophy. [provided by RefSeq, Nov 2009]
Uniprot Description
TTDN1: May play a role in maintenance of cell cycle integrity by regulating mitosis or cytokinesis. Defects in MPLKIP are a cause of trichothiodystrophy non- photosensitive type 1 (TTDN1); also known as Amish brittle hair brain syndrome (ABHS), hair-brain syndrome and BIDS syndrome. TTDN1 is an autosomal recessive disorder characterized by short stature, intellectual impairment, sulfur-deficient brittle hair and decreased male fertility but not cutaneous photosensitivity.
Protein type: Cell cycle regulation
Chromosomal Location of Human Ortholog: 7p14.1
Cellular Component: centrosome; cytoplasm; Golgi apparatus; midbody; nucleoplasm; nucleus
Molecular Function: protein binding
Disease: Trichothiodystrophy, Nonphotosensitive 1
Research Articles on MPLKIP
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Product Notes
The MPLKIP mplkip (Catalog #AAA9222695) is a Blocking Peptide and is intended for research purposes only. The product is available for immediate purchase. It is sometimes possible for the material contained within the vial of "TTDN1, Blocking Peptide" 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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