NSUN5 rabbit pAb
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. [provided by RefSeq, Jul 2013],
Product Specifications
Background
UniProt
Q96P11
Swiss Prot
Q96P11
Reactivity
Human; Mouse
Immunogen
Synthesized peptide derived from human protein . at AA range: 320-400
Target
NSUN5
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
WB 1:500-2000 ELISA 1:5000-20000
Buffer
-20°C/1 year
Molecular Weight
47kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
47kD
Fragment
IgG
Subcellular Location
Nucleus, nucleolus .
Gene ID (Human)
55695
Available Sizes
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