Rabbit Recombinant Monoclonal UGPase antibody. Suitable for IHC-P, WB, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 4 publications.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 50% Tissue culture supernatant, 40% Glycerol (glycerin, glycerine), 9% PBS, 0.05% BSA
IHC-P | IP | WB | ICC/IF | Flow Cyt (Intra) | |
---|---|---|---|---|---|
Human | Tested | Not recommended | Tested | Not recommended | Expected |
Mouse | Expected | Not recommended | Expected | Not recommended | Tested |
Rat | Predicted | Not recommended | Expected | Not recommended | Predicted |
Pig | Predicted | Not recommended | Predicted | Not recommended | Predicted |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/50 - 1/100 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat, Pig | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Human, Rat, Pig | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/1000 - 1/10000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Pig | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Human, Rat, Pig | Dilution info - | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/10 - 1/100 | Notes ab172730 - Rabbit monoclonal IgG, is suitable for use as an isotype control with this antibody. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat, Pig | Dilution info - | Notes - |
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UTP--glucose-1-phosphate uridylyltransferase catalyzing the conversion of glucose-1-phosphate into UDP-glucose, a crucial precursor for the production of glycogen.
UGP1, UGP2, UTP--glucose-1-phosphate uridylyltransferase, UDP-glucose pyrophosphorylase, UDPGP, UGPase
Rabbit Recombinant Monoclonal UGPase antibody. Suitable for IHC-P, WB, Flow Cyt (Intra) and reacts with Human, Mouse, Rat samples. Cited in 4 publications.
pH: 7.2 - 7.4
Preservative: 0.01% Sodium azide
Constituents: 50% Tissue culture supernatant, 40% Glycerol (glycerin, glycerine), 9% PBS, 0.05% BSA
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
UGPase also known as UDP-glucose pyrophosphorylase plays an important role in carbohydrate metabolism by catalyzing the reversible formation of UDP-glucose and pyrophosphate from glucose-1-phosphate and UTP. The enzyme has a mass of about 52 kDa. UGPase is expressed in many tissues but especially in liver muscle and brain where carbohydrate metabolism is highly active. Its presence ensures the availability of UDP-glucose which serves as a glycosyl donor in the synthesis of glycogen.
UGPase provides UDP-glucose a central metabolite in carbohydrate biosynthesis. It does not function as part of a complex but independently supports various biosynthetic pathways. UDP-glucose acts as a precursor not only for glycogen but also for glycoproteins glycolipids and proteoglycans. UGPase activity is critical for maintaining glucose homeostasis and its regulation directly affects carbohydrate allocation and storage.
UGPase operates in the glycogen synthesis pathway and the pentose phosphate pathway. In the glycogen synthesis pathway UGPase works closely with glycogen synthase which converts UDP-glucose into glycogen helping in energy storage. In the pentose phosphate pathway UDP-glucose serves as a substrate for enzymes modifying carbohydrate structures. These pathway interactions place UGPase as an essential node linking carbohydrate metabolism routes.
The dysregulation of UGPase affects disorders like glycogen storage diseases and diabetes. An abnormal UGPase activity can lead to inefficient glycogen storage impacting energy balance and contributing to these conditions. The enzyme also connects with proteins like glycogen synthase in glycogen storage diseases illustrating how alterations in its function can disturb glycogen synthesis and storage. Understanding UGPase activity therefore offers insights into metabolic imbalances seen in these diseases.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
We do not recommend this combination. It is not covered by our product promise.
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In the unlikely event of one of our products not working as expected, you are covered by our product promise.
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All lanes: Western blot - Anti-UGPase antibody [EPR10627(B)] (ab154817) at 1/1000 dilution
Lane 1: HepG2 cell lysate at 10 µg
Lane 2: HeLa cell lysate at 10 µg
Lane 3: NIH 3T3 cell lysate at 10 µg
Lane 4: Human fetal liver tissue lysate at 10 µg
Predicted band size: 57 kDa
Immunohistochemical analysis of paraffin-embedded Human colon adenocarcinoma labeling UGPase using ab154817 at 1/50 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Immunohistochemical analysis of paraffin-embedded Human kidney labeling UGPase using ab154817 at 1/50 dilution.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Intracellular flow cytometric analysis of permeabilized NIH 3T3 cells labeling UGPase using ab154817 (red) at 1/10 dilution or a rabbit IgG (negative) (green).
Immunohistochemical analysis of paraffin embedded Human skeletal muscle tissue using ab154817 showing +ve staining.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Immunohistochemical analysis of paraffin embedded Human normal liver tissue using ab154817 showing +ve staining.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Immunohistochemical analysis of paraffin embedded Human normal heart tissue using ab154817 showing +ve staining.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Immunohistochemical analysis of paraffin embedded Human normal colon tissue using ab154817 showing +ve staining.
Perform heat mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol.
Lanes 1 - 2: Western blot - Anti-UGPase antibody [EPR10627(B)] (ab154817) at 1/10000 dilution
Lanes 3 - 4: Western blot - Anti-UGPase antibody [EPR10627(B)] (ab154817) at 1/20000 dilution
Lanes 5 - 6: Western blot - Anti-UGPase antibody [EPR10627(B)] (ab154817)
All lanes: Pig muscle sarcoplasm tissue lysate at 40 µg
All lanes: HRP-conjugated goat anti-rabbit IgG (H+L) polyclonal at 1/10000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 57 kDa
Observed band size: 45-47 kDa
Exposure time: 5min
Image collected and cropped by CiteAb under a CC-BY license from the publication
UGPase western blot using anti-UGPase antibody [EPR10627(B)] ab154817. Publication image and figure legend from Sherman, E. J., Mirabelli, C., et al., 2022, PLoS Pathog, PubMed 35231079.
ab154817 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab154817 please see the product overview.
Interrogation of ACE2 modifiers in Calu-3 cells.(A) FACS plots of ACE2 surface staining in Calu-3 cells treated with control nontargeting (NT) or SMAD4-targeting gRNA for each of 3 technical replicates. (B) Volcano plots of MAGeCK Robust Rank Aggregation scores and gene-level gRNA log2 fold-change in ACE2negative relative to ACE2positive populations for each gene tested in the focused CRISPR library in Calu-3 cells. Genes with FDR <0.05 and absolute log2 fold-change >1 are highlighted, with positive regulators in blue and negative regulators in red. (C) Comparison of log2 fold-change in ACE2negative relative to ACE2positive populations in focused CRISPR screens of HuH7 (x-axis) and Calu-3 (y-axis). Only ACE2, highlighted in blue, was identified in both screens with FDR<0.05 and absolute log2 fold-change >1. Genes identified as significant in only the HuH7 or Calu-3 screens are highlighted in magenta and red, respectively. (D) Immunoblot of lysates collected from Calu-3 cells targeted by CRISPR with a gRNA against the indicated gene or a nontargeting (NT) control sequence. (E) Percentage of cells with detectable surface ACE2 staining after CRISPR-mediated single gene disruption of the indicated target gene or a nontargeting control in Calu-3 cells. Candidate genes associated with positive or negative regulation of ACE2 in the CRISPR screen are highlighted in blue and red, respectively. ACE2-positive gates were defined on control unstained cells and the proportion of ACE2-positive cells for each population is displayed for each of 3–6 technical replicates. Error bars depict standard deviation. Asterisks indicate p<0.05 by Student’s t-test. Source data and statistical analysis are provided in S9 Table.
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