WRNIP1 antibody (N-Term)
Quick Overview for WRNIP1 antibody (N-Term) (ABIN2775244)
Target
See all WRNIP1 AntibodiesReactivity
Host
Clonality
Conjugate
Application
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Binding Specificity
- N-Term
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Sequence
- PGAKRRRLSE SSALKQPATP TAAESSEGEG EEGDDGGETE SRESYDAPPT
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Predicted Reactivity
- Cow: 79%, Dog: 100%, Human: 100%, Mouse: 100%, Pig: 79%, Rat: 100%, Yeast: 77%, Zebrafish: 85%
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Characteristics
- This is a rabbit polyclonal antibody against WRNIP1. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogen
- The immunogen is a synthetic peptide directed towards the N terminal region of human WRNIP1
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Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
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Comment
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Antigen size: 640 AA
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- Lot specific
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Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Handling Advice
- Avoid repeated freeze-thaw cycles.
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Storage
- -20 °C
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Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
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: "Human Werner helicase interacting protein 1 (WRNIP1) functions as a novel modulator for DNA polymerase delta." in: Genes to cells : devoted to molecular & cellular mechanisms, Vol. 10, Issue 1, pp. 13-22, (2005) (PubMed).
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: "Human Werner helicase interacting protein 1 (WRNIP1) functions as a novel modulator for DNA polymerase delta." in: Genes to cells : devoted to molecular & cellular mechanisms, Vol. 10, Issue 1, pp. 13-22, (2005) (PubMed).
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- WRNIP1 (Werner Helicase Interacting Protein 1 (WRNIP1))
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Alternative Name
- WRNIP1
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Background
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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.
Alias Symbols: FLJ22526, RP11-420G6.2, WHIP, bA420G6.2
Protein Interaction Partner: UBC, RNF31, PIN1, ELP2, ELP3, TRIM28, HDAC11, EPAS1, VCP, SRSF4, SMAD2, RAD18, NUP107, WRNIP1, FGFR1OP, POLD1, ABL1, SUMO2, TOLLIP, DDX58, USP11, OSBPL10, USP25, POLD4, POLD2, WRN,
Protein Size: 640 -
Molecular Weight
- 72 kDa
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Gene ID
- 56897
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NCBI Accession
- NM_130395, NP_569079
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UniProt
- Q96S55
Target
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