Human NOP10 ribonucleoprotein homolog (yeast) ELISA Kit | NOP10 elisa kit
Human H/ACA ribonucleoprotein complex subunit 3, NOP10 ELISA Kit
NCBI and Uniprot Product Information
NCBI Description
This gene is a member of the H/ACA snoRNPs (small nucleolar ribonucleoproteins) gene family. snoRNPs are involved in various aspects of rRNA processing and modification and have been classified into two families: C/D and H/ACA. The H/ACA snoRNPs also include the DKC1, NOLA1 and NOLA2 proteins. These four H/ACA snoRNP proteins localize to the dense fibrillar components of nucleoli and to coiled (Cajal) bodies in the nucleus. Both 18S rRNA production and rRNA pseudouridylation are impaired if any one of the four proteins is depleted. The four H/ACA snoRNP proteins are also components of the telomerase complex. This gene encodes a protein related to Saccharomyces cerevisiae Nop10p. [provided by RefSeq, Jul 2008]
Uniprot Description
NOP10: Required for ribosome biogenesis and telomere maintenance. Part of the H/ACA small nucleolar ribonucleoprotein (H/ACA snoRNP) complex, which catalyzes pseudouridylation of rRNA. This involves the isomerization of uridine such that the ribose is subsequently attached to C5, instead of the normal N1. Each rRNA can contain up to 100 pseudouridine (psi) residues, which may serve to stabilize the conformation of rRNAs. May also be required for correct processing or intranuclear trafficking of TERC, the RNA component of the telomerase reverse transcriptase (TERT) holoenzyme. Defects in NOP10 are a cause of dyskeratosis congenita autosomal recessive type 1 (DKCB1). A rare multisystem disorder caused by defective telomere maintenance. It is characterized by progressive bone marrow failure, and the clinical triad of reticulated skin hyperpigmentation, nail dystrophy, and mucosal leukoplakia. Common but variable features include premature graying, aplastic anemia, low platelets, osteoporosis, pulmonary fibrosis, and liver fibrosis among others. Early mortality is often associated with bone marrow failure, infections, fatal pulmonary complications, or malignancy. Belongs to the NOP10 family.
Protein type: Nucleolus
Chromosomal Location of Human Ortholog: 15q14-q15
Cellular Component: Cajal body; small nucleolar ribonucleoprotein complex; nucleolus
Molecular Function: snoRNA binding; protein binding
Biological Process: pseudouridine synthesis; rRNA processing
Disease: Dyskeratosis Congenita, Autosomal Recessive, 1
Research Articles on NOP10
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Product Notes
The Human NOP10 nop10 (Catalog #AAA9337821) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA9337821 ELISA Kit recognizes Human NOP10. It is sometimes possible for the material contained within the vial of "NOP10 ribonucleoprotein homolog (yeast), 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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