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HPA041091
WD repeat domain 34

Anti-WDR34 Antibody

Polyclonal Antibody against HUMAN WDR34

0.2 mg/ml
In Stock (10+)
Delivery time: Ready to Ship
4 570,0 kr
Lowest price during the previous 30 days before discount: 4 352,0 kr
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Immunohistochemical staining of human stomach shows strong cytoplasmic positivity in glandular cells.

Immunohistochemical staining of human stomach shows strong cytoplasmic positivity in glandular cells.

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Product details

  • Target protein: WD repeat domain 34
  • Target gene: WDR34
  • Verified species reactivity: Human
  • Interspecies information: Highest antigen sequence indentity to the following orthologs: MOUSE - ENSMUSG00000039715 (84%)RAT - ENSRNOG00000015636 (83%)
  • Clonality: Polyclonal
  • Isotype: IgG
  • Host: Rabbit
  • Buffer: 40% glycerol and PBS (pH 7.2). 0.02% sodium azide is added as preservative.
    Material Safety Data Sheet
  • Purification method: Affinity purified using the PrEST antigen as affinity ligand
  • Antigen sequence: Recombinant Protein Epitope Signature Tag (PrEST) antigen sequence
  • LRRVEAMVIRELNKNWQSHAFDGFEVNWTEQQQMVSCLYTLGYPPAQAQGLHVTSISWNSTGSVVACAYGRLDHGDWSTLKSFVCAWNLDRRDLR
  • Notes: Gently mix before use. Optimal concentrations and conditions for each application should be determined by the user.

Current lot

  • Unit size: 100µl
  • Current lot: R37396
  • Concentration: 0.2 mg/ml

Applications

  • Immunofluorescence in Cell Lines (ICC-IF) recommended conditions
    • Working concentration: 0.25-2 µg/ml
    • Fixation/Permeabilization: PFA/Triton X-100
  • Immunohistochemistry (IHC) recommended conditions
    • Dilution: 1:50 - 1:200
    • Retrieval method: HIER pH6

Target information

  • Protein name: WD repeat domain 34
  • Gene name: WDR34
  • Alternative gene names: bA216B9.3DIC5FAP133MGC20486
  • Ensembl: ENSG00000119333
  • Entrez: 89891
  • UniProt: Q96EX3

Shipping and storage

  • Shipping: Normally shipped at ambient temperatureStorage: Store at +4°C for short term storage. Long time storage is recommended at -20°C.

References (3)

  • Mutations in GRK2 cause Jeune syndrome by impairing Hedgehog and canonical Wnt signalingBosakova M, Abraham SP, Nita A, Hruba E, Buchtova M, Taylor SP, Duran I, Martin J, Svozilova K, Barta T, Varecha M, Balek L, Kohoutek J, Radaszkiewicz T, Pusapati GV, Bryja V, Rush ET, Thiffault I, Nickerson DA, Bamshad MJ, University of Washington Center for Mendelian Genomics, Rohatgi R, Cohn DH, Krakow D, Krejci PEMBO Mol Med , 2020 Oct 14; 12(11):e11739. Epub 2020 Oct 142020 Oct 14
  • Mutations in DYNC2LI1 disrupt cilia function and cause short rib polydactyly syndromeTaylor SP, Dantas TJ, Duran I, Wu S, Lachman RS, University of Washington Center for Mendelian Genomics, Nelson SF, Cohn DH, Vallee RB, Krakow DNat Commun , 2015 Jun 16; 6:7092. Epub 2015 Jun 162015 Jun 16
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