NSUN5 polyclonal antibody
Product Specifications
Background
This gene encodes a member of an evolutionarily conserved family of proteins that may function as methyltransferases. This gene is located in a larger region of chromosome 7 that is deleted in Williams-Beuren syndrome, a multisystem developmental disorder. There are two pseudogenes for this gene located in the same region of chromosome 7. Alternative splicing results in multiple transcript variants encoding different isoforms.
CAS Number
9007-83-4
Structure Composition
1mg/ml in PBS with 0.02% sodium azide, 50% glycerol, pH7.2
Product Name Alternative
NSUN5; NOL1; NOL1R; NSUN5A; WBSCR20; WBSCR20A; p120; p120 (NOL1)
Swiss Prot
Q96P11
Reactivity
Human, Mouse, Rat
Immunogen
Recombinant fusion protein of human NSUN5 (NP_060514.1) .
Conjugation
Unconjugated
Applications
WB, IHC
Dilution
WB,1:200 - 1:2000|IHC,1:50 - 1:200
Purity
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen and the purity is > 95% (by SDS-PAGE) .
Modification
Unmodification
Molecular Weight
47kDa
Storage Conditions
Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.
Notes
For research use only, not for use in diagnostic procedure.
Specificity
Unmodification
Host or Source
Rabbit
Available Sizes
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