PNPLA6 blocking peptide

PNPLA6 Blocking Peptide

Cat. Num. AAA8236817

• Gene Names: PNPLA6; NTE; sws; BNHS; LNMS; OMCS; SPG39; NTEMND; iPLA2delta
• Reactivity: Human, Mouse
• Applications: Blocking (BL)
• Purity: >85%
• Synonyms: PNPLA6; PNPLA6 Blocking Peptide; NTE; Neuropathy target esterase; Patatin-like phospholipase domain-containing protein 6; PNPLA6 blocking peptide

• Host: Synthetic
• Reactivity: Human, Mouse
• Purity/Purification: >85%
• Form/Format: Lyophilized powder
• Sequence Length: 1,300

• Applicable Applications for PNPLA6 blocking peptide: Blocking (BL)
• Quality Control: The quality of the peptide was evaluated by reversed-phase HPLC and by mass spectrometry.
• Directions for Use: Blocking Peptide to the diluted primary antibody in a molar ratio of 10:1 (peptide to antibody) and incubate the mixture at 4 degree C for overnight or at room temperature for 2 hours.
• Preparation and Storage: Shipped at 4 degree C. Store at -20 degree C for one year.

Related Product Information for PNPLA6 blocking peptide

The peptide is used to block Anti-PNPLA6 Antibody reactivity.

NCBI and Uniprot Product Information

• NCBI GI #: 260656037
• NCBI GeneID: 10908
• NCBI Accession #: NP_001159583.1
• NCBI GenBank Nucleotide #: NM_001166111.1
• UniProt Accession #: Q8IY17; O60859; Q86W58; Q9UG58; A6NGQ0; B4DFB9; B7Z7T2; F5H5K9; J3KQS3
• Molecular Weight: 143,351 Da
• NCBI Official Full Name: neuropathy target esterase isoform a
• NCBI Official Synonym Full Names: patatin-like phospholipase domain containing 6
• NCBI Official Symbol: PNPLA6
• NCBI Official Synonym Symbols: NTE; sws; BNHS; LNMS; OMCS; SPG39; NTEMND; iPLA2delta
• NCBI Protein Information: neuropathy target esterase
• UniProt Protein Name: Neuropathy target esterase
• Protein Family: Neuropathy target esterase
• UniProt Gene Name: PNPLA6
• UniProt Synonym Gene Names: NTE
• UniProt Entry Name: PLPL6_HUMAN

NCBI Description

This gene encodes a phospholipase that deacetylates intracellular phosphatidylcholine to produce glycerophosphocholine. It is thought to function in neurite outgrowth and process elongation during neuronal differentiation. The protein is anchored to the cytoplasmic face of the endoplasmic reticulum in both neurons and non-neuronal cells. Mutations in this gene result in autosomal recessive spastic paraplegia, and the protein is the target for neurodegeneration induced by organophosphorus compounds and chemical warfare agents. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2009]

Uniprot Description

NTE: Phospholipase B that deacylates intracellular phosphatidylcholine (PtdCho), generating glycerophosphocholine (GroPtdCho). This deacylation occurs at both sn-2 and sn-1 positions of PtdCho. Its specific chemical modification by certain organophosphorus (OP) compounds leads to distal axonopathy. Defects in PNPLA6 are the cause of spastic paraplegia autosomal recessive type 39 (SPG39); also known as NTE-related motor neuron disorder (NTEMND). Spastic paraplegia is a neurodegenerative disorder characterized by a slow, gradual, progressive weakness and spasticity of the lower limbs. Rate of progression and the severity of symptoms are quite variable. Initial symptoms may include difficulty with balance, weakness and stiffness in the legs, muscle spasms, and dragging the toes when walking. In some forms of the disorder, bladder symptoms (such as incontinence) may appear, or the weakness and stiffness may spread to other parts of the body. SPG39 is associated with a motor axonopathy affecting upper and lower limbs and resulting in progressive wasting of distal upper and lower extremity muscles. Belongs to the NTE family. 3 isoforms of the human protein are produced by alternative splicing.

Protein type: Hydrolase; Membrane protein, integral; EC 3.1.1.5

Chromosomal Location of Human Ortholog: 19p13.2

Cellular Component: endoplasmic reticulum membrane; membrane; endoplasmic reticulum; integral to membrane

Molecular Function: lysophospholipase activity

Biological Process: organ morphogenesis; angiogenesis; developmental process; lipid catabolic process; phosphatidylcholine metabolic process

Disease: Laurence-moon Syndrome; Spastic Paraplegia 39, Autosomal Recessive; Oliver-mcfarlane Syndrome; Boucher-neuhauser Syndrome