SKU: WP6110 Categories: ,

ZRANB3 rabbit pAb

Price range: $268.00 through $328.00

SKU: WP6110-100
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Product details

Background:

Specifications

Size50μL/100μL
TargetZRANB3
ReactivityHuman, Mouse
ApplicationsWB
MW(Calculated)119kD
MW(Observed)
Host SpeciesRabbit
IsotypeIgG
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-2000
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration1 mg/ml
ClonalityPolyclonal
Clone Number
ImmunogenSynthesized peptide derived from human ZRANB3
SpecificityThis antibody detects endogenous levels of ZRANB3 at Human, Mouse
Gene NameZRANB3
Protein NameDNA annealing helicase and endonuclease ZRANB3 (Annealing helicase 2) (AH2) (Zinc finger Ran-binding domain-containing protein 3) [Includes: DNA annealing helicase ZRANB3 (EC 3.6.4.-); Endonuclease ZRANB3 (EC 3.1.-.-)]
Other Name
SpeciesHuman
Gene ID84083
UniprotQ5FWF4,
Species.1Mouse
Gene ID.1226409
Uniprot.1Q6NZP1
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationNucleus . Chromosome . Following DNA damage, recruited to sites of DNA damage and stalled replication forks by polyubiquitinated PCNA (PubMed:22704558, PubMed:22705370, PubMed:22759634). .
Tissue Expression
Signaling_pathway
Research Areas
FunctionDNA annealing helicase and endonuclease required to maintain genome stability at stalled or collapsed replication forks by facilitating fork restart and limiting inappropriate recombination that could occur during template switching events . Recruited to the sites of stalled DNA replication by polyubiquitinated PCNA and acts as a structure-specific endonuclease that cleaves the replication fork D-loop intermediate, generating an accessible 3'-OH group in the template of the leading strand, which is amenable to extension by DNA polymerase . In addition to endonuclease activity, also catalyzes the fork regression via annealing helicase activity in order to prevent disintegration of the replication fork and the formation of double-strand breaks .
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