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C3orf58 Polyclonal Antibody

Purified Rabbit Polyclonal Antibody (Pab)

     
  • WB - C3orf58 Polyclonal Antibody AP55854
    Sample: TT(human) Cell Lysate at 40 ug
    Primary: Anti-C3orf58 (bs-15179R) at 1/300 dilution
    Secondary: IRDye800CW Goat Anti-Rabbit IgG at 1/20000 dilution
    Predicted band size: 49 kD
    Observed band size: 48 kD
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Product Information
Application
  • 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
  • E=ELISA
  • IP=Immunoprecipitation
  • DB=Dot Blot
  • CHIP=Chromatin Immunoprecipitation
  • FA=Fluorescence Assay
  • IEM=Immuno electron microscopy
  • EIA=Enzyme Immunoassay
WB, IHC-P, IHC-F, IF, ICC
Primary Accession Q8NDZ4
Reactivity Rat, Bovine
Host Rabbit
Clonality Polyclonal
Calculated MW 49 KDa
Physical State Liquid
Immunogen KLH conjugated synthetic peptide derived from human C3orf58
Epitope Specificity 351-430/430
Isotype IgG
Purity affinity purified by Protein A
Buffer 0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
Background Descriptions C3orf58 (chromosome 3 open reading frame 58), also known as DIA1, is a 430 amino acid secreted protein that belongs to the UPF0672 family. C3orf58 is encoded by a gene that maps to human chromosome 3q24. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.
Additional Information
Gene ID 205428
Other Names Divergent protein kinase domain 2A, Deleted in autism protein 1, Golgi Protein of 49 kDa, GoPro49, Hypoxia and AKT-induced stem cell factor, HASF, DIPK2A (HGNC:28490)
Dilution WB=1:500-2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC=1:100-500,IF=1:100-500
StorageStore at -20 ℃ for one year. Avoid repeated freeze/thaw cycles. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 ℃.
Protein Information
Name DIPK2A (HGNC:28490)
Function May play a role in cardiomyocyte proliferation through paracrine signaling and activation of the PPI3K-AKT-CDK7 signaling cascade.
Cellular Location Cytoplasmic vesicle, COPI-coated vesicle. Golgi apparatus. Secreted
Research Areas
Citations (0)
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$ 385.00
Cat# AP55854
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