NIPA1 polyclonal antibody
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More Files
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human urinary bladder with NIPA1 polyclonal antibody (Cat # PAB21503) shows strong membranous positivity in urothelial cells at 1:10-1:20 dilution.
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Specification
Product Description
Rabbit polyclonal antibody raised against recombinant NIPA1.
Immunogen
Recombinant protein corresponding to amino acids of human NIPA1.
Sequence
HGPTNIMVYISICSLLGSFTVPSTKGIGLAAQDILHNNPSSQRA
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Antigen affinity purification
Isotype
IgG
Recommend Usage
Immunohistochemistry (1:10-1:20)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS, pH 7.2 (40% glycerol, 0.02% 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
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Immunohistochemical staining of human urinary bladder with NIPA1 polyclonal antibody (Cat # PAB21503) shows strong membranous positivity in urothelial cells at 1:10-1:20 dilution. -
Gene Info — NIPA1
Entrez GeneID
123606Protein Accession#
Q7RTP0Gene Name
NIPA1
Gene Alias
FSP3, MGC102724, MGC35570, SPG6
Gene Description
non imprinted in Prader-Willi/Angelman syndrome 1
Gene Ontology
HyperlinkGene Summary
This gene encodes a magnesium transporter that associates with early endosomes and the cell surface in a variety of neuronal and epithelial cells. This protein may play a role in nervous system development and maintenance. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene have been associated with autosomal dominant spastic paraplegia 6. [provided by RefSeq
Other Designations
non-imprinted in Prader-Willi/Angelman syndrome 1|spastic paraplegia 6 (autosomal dominant)
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Interactome
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Disease
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