UMPS-Polyclonal Antibodies

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UMPS

Qty


Total
$220
Catalog #
A5492
Antibody Type
Polyclonal Antibody
Gene ID
7372
Swiss Prot
P11172
Size
Species
Rabbit
Isotype
IgG
Purity
Affinity purification
Additional Information
ReactivityHuman Mouse Rat
Tested applicationsWB IHC IF
Recommended DilutionWB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:50 - 1:100
Calculated MW52kDa
Observed MWRefer to figures
ImmunogenRecombinant protein of human UMPS
Storage BufferStore at -20℃. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3.
SynonymOPRT;
Images
  • A5492: image 1

    Western blot analysis of extracts of Jurkat cells, using UMPS antibody.

  • A5492: image 2

    Immunohistochemistry of paraffin-embedded rat liver using UMPS antibody at dilution of 1:200 (400x lens).

  • A5492: image 3

    Immunohistochemistry of paraffin-embedded rat brain using UMPS antibody at dilution of 1:200 (400x lens).

  • A5492: image 4

    Immunohistochemistry of paraffin-embedded mouse kidney using UMPS antibody at dilution of 1:200 (400x lens).

  • A5492: image 5

    Immunohistochemistry of paraffin-embedded mouse brain using UMPS antibody at dilution of 1:200 (400x lens).

  • A5492: image 6

    Immunohistochemistry of paraffin-embedded human colon damage using UMPS antibody at dilution of 1:200 (400x lens).

  • A5492: image 7

    Immunohistochemistry of paraffin-embedded human normal stomach using UMPS antibody at dilution of 1:200 (400x lens).

  • A5492: image 8

    Immunofluorescence analysis of HeLa cell using UMPS antibody.

Background

This gene encodes a uridine 5'-monophosphate synthase. The encoded protein is a bifunctional enzyme that catalyzes the final two steps of the de novo pyrimidine biosynthetic pathway. The first reaction is carried out by the N-terminal enzyme orotate phosphoribosyltransferase which converts orotic acid to orotidine-5'-monophosphate. The terminal reaction is carried out by the C-terminal enzyme OMP decarboxylase which converts orotidine-5'-monophosphate to uridine monophosphate. Defects in this gene are the cause of hereditary orotic aciduria. Alternate splicing results in multiple transcript variants.

Protocol

N/A

MSDS
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