NPAP1 Polyclonal Antibody
Product Specifications
Background
This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome. May be involved in spermatogenesis.
Synonyms
NPAP1; NPAP 1; NPAP-1; Nuclear pore associated protein 1; NPAP1_HUMAN; C15orf2.
Gene ID
23742
Swiss Prot
Q9NZP6
Cellular Locus
Nucleus
Host
Rabbit
Cross Reactivity
Human
Immunogen
801-900/1156
Target
NPAP1
Clonality
Polyclonal
Conjugation
Unconjugated
Source
KLH conjugated synthetic peptide derived from human NPAP1
Applications
WB, IHC-P, IF (IHC-P)
Purification
Purified by Protein A.
Concentration
1ug/ul
Dilution
WB (1:300-5000), IHC-P (1:200-400), IF (IHC-P) (1:50-200)
Buffer
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Modification
Unmodified
Storage Conditions
Shipped at 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.
Gene ID URL
23742
Isotype
IgG
Curated Selection
Explore Other Products
Discover premium biology products from our extensive collection of 20M+ items
GTR15137382 1 Vial
Lentiviral human ATXN7L3 shRNA (UAS) - Lentiviral human ATXN7L3 shRNA (UAS) (100)
Ask
View Details 