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>   home   >   Products   >   Primary Antibodies   >   Signal Transduction   >   DNAJC30 Antibody (C-term)   

DNAJC30 Antibody (C-term)

Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

  • WB - DNAJC30 Antibody (C-term) AP18088b
    DNAJC30 Antibody (C-term) (Cat. #AP18088b) western blot analysis in HL-60 cell line lysates (35ug/lane).This demonstrates the DNAJC30 antibody detected the DNAJC30 protein (arrow).
Product Information
  • Applications Legend:
  • WB=Western Blot
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin-embedded Sections)
  • IHC-F=Immunohistochemistry (Frozen Sections)
  • IF=Immunofluorescence
  • FC=Flow Cytopmetry
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immunoelectronmicroscopy
  • EIA=Enzyme Immunoassay
Primary Accession Q96LL9
Other Accession NP_115693.2
Reactivity Human
Host Rabbit
Clonality Polyclonal
Isotype Rabbit Ig
Calculated MW 25961 Da
Antigen Region 176-202 aa
Additional Information
Gene ID 84277
Other Names DnaJ homolog subfamily C member 30, Williams-Beuren syndrome chromosomal region 18 protein, DNAJC30, WBSCR18
Target/Specificity This DNAJC30 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 176-202 amino acids from the C-terminal region of human DNAJC30.
Dilution WB~~1:1000
Format Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
StorageMaintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
PrecautionsDNAJC30 Antibody (C-term) is for research use only and not for use in diagnostic or therapeutic procedures.
Protein Information
Name DNAJC30
Synonyms WBSCR18
Tissue Location Expressed in brain, heart, kidney, liver, lung, spleen, stomach and testis.
Research Areas
Citations (0)

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This intronless gene encodes a member of the DNAJ molecular chaperone homology domain-containing protein family. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23.


Lamesch, P., et al. Genomics 89(3):307-315(2007)
Lehner, B., et al. Genome Res. 14(7):1315-1323(2004)
Merla, G., et al. Hum. Genet. 110(5):429-438(2002)

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$ 295.00
$ 99.00
Cat# AP18088b
(40 western blots)
Availability: In Stock
Bulk Size
Seasonal Special on Bulk Order
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