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WRNIP1 Rabbit anti-Human, Polyclonal Antibody, Abnova™
Rabbit polyclonal antibody raised against recombinant WRNIP1.
Supplier: Abnova Corporation PAB22586
Description
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. [provided by RefSeq]
Sequence: YQGCHFIGMPECEVLLAQCVVYFARAPKSIEVYSAYNNVKARLRNHQGPLPPVPLHLRNAPTRLMKDLGYGSpecifications
WRNIP1 | |
Polyclonal | |
Rabbit polyclonal antibody raised against recombinant WRNIP1. | |
In PBS, pH 7.5 (40% glycerol, 0.02% sodium azide) | |
FLJ22526/RP11-420G6.2/WHIP/bA420G6.2 | |
Rabbit | |
Antigen affinity purification | |
RUO | |
56897 | |
Store at 4°C. For long term storage store at -20°C. Aliquot to avoid repeated freezing and thawing. |
|
IgG |
Immunofluorescence, Immunohistochemistry (PFA fixed), Western Blot | |
Unconjugated | |
Immunohistochemistry (1:10-1:20) Western Blot (1:250-1:500) Immunofluorescence (1-4 ug/mL) The optimal working dilution should be determined by the end user. | |
WRNIP1 | |
WRNIP1 | |
Recombinant protein corresponding to amino acids of human WRNIP1. | |
100 μL | |
Primary | |
Human | |
Liquid |
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For Research Use Only