PANK2 polyclonal antibody
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More Files
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of PANK2.
Immunogen
A synthetic peptide (conjugated with KLH) corresponding to amino acids 65-95 at N-terminus of human PANK2.
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Protein G purification
Recommend Usage
ELISA
Western Blot (1:1000)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.09% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Tissue lysate)
Western blot analysis of PANK2 polyclonal antibody (Cat # PAB2719) in mouse liver tissue lysate (35 ug/lane). PANK2 (arrow) was detected using the purified polyclonal abtibody. -
Gene Info — PANK2
Entrez GeneID
80025Protein Accession#
AAN32907;Q9BZ23Gene Name
PANK2
Gene Alias
C20orf48, FLJ17232, HARP, HSS, MGC15053, NBIA1, PKAN
Gene Description
pantothenate kinase 2
Gene Ontology
HyperlinkGene Summary
This gene encodes a protein belonging to the pantothenate kinase family and is the only member of that family to be expressed in mitochondria. Pantothenate kinase is a key regulatory enzyme in the biosynthesis of coenzyme A (CoA) in bacteria and mammalian cells. It catalyzes the first committed step in the universal biosynthetic pathway leading to CoA and is itself subject to regulation through feedback inhibition by acyl CoA species. Mutations in this gene are associated with HARP syndrome and pantothenate kinase-associated neurodegeneration (PKAN), formerly Hallervorden-Spatz syndrome. Alternative splicing, involving the use of alternate first exons, results in multiple transcripts encoding different isoforms. [provided by RefSeq
Other Designations
Hallervorden-Spatz syndrome|OTTHUMP00000030143|OTTHUMP00000030148|pantothenic acid kinase
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Interactome
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Pathway
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Disease
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Publication Reference
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Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic.
Houlden H, Lincoln S, Farrer M, Cleland PG, Hardy J, Orrell RW.
Neurology 2003 Nov; 61(10):1423.
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An isoform of hPANK2, deficient in pantothenate kinase-associated neurodegeneration, localizes to mitochondria.
Hortnagel K, Prokisch H, Meitinger T.
Human Molecular Genetics 2003 Feb; 12(3):321.
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Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic.
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