TUFM Peptide - middle region (AAP58546)

Data Sheet
 
Sku AAP58546
Old sku AAPP34728
Price $99.00
Name TUFM Peptide - middle region (AAP58546)
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Size 100 ug
Gene TUFM
Alias symbols COXPD4, EF-TuMT, EFTU, P43
Gene id 7284
Description of target TUFM is a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Swissprot id P49411
Protein accession num NP_003312
Nucleotide accession num NM_003321
Protein size 455 amino acids
Molecular weight 50kDa
Application WB
Partner proteins ATP6V1A,MYH9,SGK1
Quality control The peptide is characterized by mass spectroscopy
Key reference Valente,L., (2007) Am. J. Hum. Genet. 80 (1), 44-58
Description This is a synthetic peptide designed for use in combination with anti-TUFM antibody (Catalog #: ARP58546_P050) made by Aviva Systems Biology. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications. Please inquire for more details.
Product format Lyophilized powder
Reconstitution and storage Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20C. Avoid repeat freeze-thaw cycles.
Lead time Domestic: within 24 hours delivery  International: 3-5 business days
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