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Antibody used in WB on Human HepG2 at 0.2-1 ug/ml.
Antibody used in WB on Human at 1:1000.
Antibody used in WB on Human HepG2 at 0.2-1 ug/ml.

WRNIP1 Antibody

CATALOG NUMBER: 28-498

Clonality:
Polyclonal
Tested Applications:
ELISA, WB
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Conjugate:
Unconjugated
Specifications
Host Species:
Rabbit
Species Reactivity:
Human, Mouse, Rat
Immunogen:
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human WRNIP1.
Conjugate:
Unconjugated
Tested Applications:
ELISA, WB
Application Note:
WRNIP1 antibody can be used for detection of WRNIP1 by ELISA at 1:62500. WRNIP1 antibody can be used for detection of WRNIP1 by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Positive Control 1:
Cat. No. 1205 - Jurkat Cell Lysate
Predicted Molecular Weight:
72 kDa
Purification:
Antibody is purified by peptide affinity chromatography method.
Clonality:
Polyclonal
Physical State:
Liquid
Buffer:
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Concentration:
batch dependent
Storage Conditions:
For short periods of storage (days) store at 4°C. For longer periods of storage, store WRNIP1 antibody at -20°C. As with any antibody avoid repeat freeze-thaw cycles.
Ncbi Official Symbol:
WRNIP1
Additional Names:
WRNIP1, FLJ22526, RP11-420G6.2, WHIP, bA420G6.2
Protein Accession Number:
NP_064520
Protein Gi Number:
18426902
Ncbi Gene Id Number:
56897
User Note:
Optimal dilutions for each application to be determined by the researcher.
Background:
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.
Background Reference 1:
Bish, R.A. (2007) J. Biol. Chem. 282 (32), 23184-23193.

FOR RESEARCH USE ONLY

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Disclaimer:
This product is for research use only.

CATALOG NUMBER:

28-498

List Size:
100 ul

List Price:

$519.00

Datasheet
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