Werner's syndrome is a rare autosomal recessive disorder characterized by premature aging.
The protein encoded by this gene interacts with the N-terminal portion of Werner protein containing the exonuclease domain.
This protein shows homology to replication factor C family proteins, and is conserved from E.
coli to human.
Studies in yeast suggest that this gene may influence the aging process.
Two transcript variants encoding different isoforms have been isolated for this gene.Werner's syndrome is a rare autosomal recessive disorder characterized by premature aging.
The protein encoded by this gene interacts with the N-terminal portion of Werner protein containing the exonuclease domain.
This protein shows homology to replication factor C family proteins, and is conserved from E.
coli to human.
Studies in yeast suggest that this gene may influence the aging process.
Two transcript variants encoding different isoforms have been isolated for this gene.
Applications:Suitable for use in Western Blot.
Other applications not tested.
Recommended Dilution:Optimal dilutions to be determined by the researcher.
Storage and Stability:May be stored at 4°C for short-term only.
Aliquot to avoid repeated freezing and thawing.
Store at -20°C.
Aliquots are stable for 12 months after receipt.
For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.
仕様
Size：100ul
Host：rabbit
Source Antibody：human
Grade：Affinity Purified
Purity：Purified by affinity chromatography.
Form：Supplied as a liquid in PBS, 2% sucrose, 0.09% sodium azide.
Specificity：Recognizes human WRNIP1.
Isotype：IgG
Calc Applications Abbrev：WB
Calc Crossreactivity：Hu
Immunogen：Synthetic peptide corresponding to the N-terminal region of human WRNIP1
