PNKD blocking peptide

PNKD Peptide - N-terminal region

Cat. Num. AAA3232584

• Gene Names: PNKD; MR1; PDC; DYT8; FPD1; MR-1; BRP17; MR-1S; PKND1; PNKD1; FKSG19; TAHCCP2; KIPP1184
• Reactivity: Human
• Applications: Western Blot
• Synonyms: PNKD; PNKD Peptide - N-terminal region; PNKD blocking peptide

• Reactivity: Human
• Form/Format: Lyophilized powder
• Sequence: Synthetic peptide located within the following region: KGRGARNARVLRGILAGATANKASHNRTRALQSHSSPEGKEEPEPLSPEL
• Sequence Length: 142

• Applicable Applications for PNKD blocking peptide: Western Blot (WB)
• Preparation and Storage: Add 100ul of sterile PBS. Final peptide concentration is 1 mg/ml in PBS. For longer periods of storage, store at -20 degree C. Avoid repeat freeze-thaw cycles.

Related Product Information for PNKD blocking peptide

This is a synthetic peptide designed for use in combination with anti-PNKD Antibody, made

Target Description: This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants.

Product Categories/Family for PNKD blocking peptide

Peptide

NCBI and Uniprot Product Information

• NCBI GI #: 116642885
• NCBI GeneID: 25953
• NCBI Accession #: NP_001070867.1
• NCBI GenBank Nucleotide #: NM_001077399.2
• UniProt Accession #: Q8N490
• Molecular Weight: 15kDa
• NCBI Official Full Name: probable hydrolase PNKD isoform 3
• NCBI Official Synonym Full Names: PNKD metallo-beta-lactamase domain containing
• NCBI Official Symbol: PNKD
• NCBI Official Synonym Symbols: MR1; PDC; DYT8; FPD1; MR-1; BRP17; MR-1S; PKND1; PNKD1; FKSG19; TAHCCP2; KIPP1184
• NCBI Protein Information: probable hydrolase PNKD
• UniProt Protein Name: Probable hydrolase PNKD
• Protein Family: Probable hydrolase
• UniProt Gene Name: PNKD
• UniProt Synonym Gene Names: KIAA1184; MR1; TAHCCP2; MR-1

NCBI Description

This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]

Uniprot Description

Probable hydrolase that plays an aggravative role in the development of cardiac hypertrophy via activation of the NF-kappa-B signaling pathway.