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Read our guarantee »Anti-AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) antibody
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Rabbit polyclonal to AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491)
ab39400 detects endogenous levels of AMPK alpha 1 + AMPK alpha 2 only when phosphorylated at Serine 485 or Serine 491.
IHC-Fr, ICC/IF, WB, ELISA, IHC-Pmore details
Reacts with
Mouse, Rat, Human
Synthetic synthesized phosphopeptide derived from human AMPK1/AMPK2 around the phosphorylation site of Serine 485/491.
IHC: human colon carcinoma WB: lysate of HeLa cells treated with heat shock
Liquid
Shipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
Preservative: 0.02% Sodium Azide
Constituents: 50% Glycerol, PBS, 150mM Sodium chloride, pH 7.4
Concentration information loading...
Immunogen affinity purified
The antibody against non phosphopeptide was removed by chromatography using non phosphopeptide corresponding to the phosphorylation site.
Polyclonal
IgG
Metabolism >> Types of disease >> Cancer
Metabolism >> Pathways and Processes >> Metabolism processes >> Hypoxia
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Energy transfer pathways >> Integration of energy
Metabolism >> Pathways and Processes >> Metabolic signaling pathways >> Lipid and lipoprotein metabolism >> Fatty acids
Cancer >> Cancer Metabolism >> Response to hypoxia
Cancer >> Cancer Metabolism >> Metabolic signaling pathway >> Integration of energy metabolism
Cardiovascular >> Lipids / Lipoproteins >> Fatty Acids >> Metabolism
Neuroscience >> Neurology process >> Metabolism
Signal Transduction >> Protein Phosphorylation >> Ser / Thr Kinases >> Other Kinases
Immunohistochemistry (Paraffin-embedded sections) - AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) antibody (ab39400)
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Immunohistochemistry (Frozen sections) - AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) antibody (ab39400)
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Immunocytochemistry/ Immunofluorescence - AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) antibody (ab39400)
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Our Abpromise guarantee covers the use of ab39400 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-Fr: Use at an assay dependent concentration.
ICC/IF: Use at an assay dependent concentration.
WB: 1/5000 - 1/1000. Predicted molecular weight: 62 kDa.
ELISA: 1/20000.
IHC-P: 1/50 - 1/100.
AMP-activated protein kinase (AMPK) is a metabolic and stress-sensing kinase that regulates homeostatis, and a key target for treating Type 2 diabetes and obesity. AMPK exists as a heterotrimeric complex comprised of catalytic alpha subunits (62 kDa) and non-catalytic beta and gamma subunits. Alpha subunit has at least two isoforms (alpha 1 and alpha 2) which differ in their subcellular localization and AMP-dependence. AMPK is phosphorylated by upstream kinases, AMPK Kinase (AMPKK) and LKB1 which results in its activation. Active AMPK regulates metabolism by phosphorylating rate-limiting enzymes in metabolic pathways and controlling gene expression. Phosphorylation of threonine 172 in the activation loop of the alpha subunit is a key determinant of AMPK activity.
Cytoplasmic
Immunohistochemistry (Paraffin-embedded sections) - AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) antibody (ab39400)
Immunohistochemical analysis of paraffin embedded human colon carcinoma, using ab39400 at a 1/100 dilution. Left: Untreated; Right: Treated with synthesized phosphopeptide.
Immunohistochemistry (Frozen sections) - AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) antibody (ab39400)

ab39400 staining AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) in mouse liver tissue sections by IHC-Fr (formaldehyde-fixed frozen sections). Tissue samples were fixed with formaldehyde and blocked with 2% BSA for 30 minutes at 20°C. The sample was incubated with primary antibody (1/200 in PBS) at 4°C for 9 hours. An Alexa Fluor®488-conjugated Goat polyclonal to rabbit IgG (1/200) was used as secondary antibody. Nuclei were stained with DAPI.
This image is courtesy of an anonymous Abreview
Immunocytochemistry/ Immunofluorescence - AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) antibody (ab39400)

ab39400 staining AMPK alpha 1 + AMPK alpha 2 in human 293ft cells by Immunocytochemistry/ Immunofluorescence. The cells were paraformaldehyde fixed, permeabilised in 0.1% Triton X-100 and then blocked using 5% serum for 1 hour at 25°C. Samples were then incubated with primary antibody at 1/100 for 2 hours at 25°C. The secondary antibody used was a goat anti-rabbit IgG conjugated to Alexa Fluor® 488 (green) used at a 1/250 dilution. DAPI was used to stain the cell nuclei (blue).
This image is courtesy of an anonymous abreview.
Western blot - AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) antibody (ab39400)

Anti-AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) antibody (ab39400) at 1/2000 dilution (in PBS-T for 12 hours at 4°C) + Whole cell lysate of mouse liver at 50 µg
Secondary
An HRP-conjugated Goat anti-rabbit IgG polyclonal at 1/5000 dilution
developed using the ECL technique
Performed under reducing conditions.
Predicted band size : 62 kDa
Exposure time : 30 seconds
Blocking Step: 5% Milk for 2 hours at 25°C
This image is courtesy of an anonymous Abreview
ab39400 has not yet been referenced specifically in any publications.
Publishing research using ab39400? Please let us know so that we can cite the reference in this datasheet
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Immunohistochemical analysis of paraffin embedded human colon carcinoma, using ab39400 at a 1/100 dilution. Left: Untreated; Right: Treated with synthesized phosphopeptide.

ab39400 staining AMPK alpha 1 + AMPK alpha 2 (phospho S485 + S491) in mouse liver tissue sections by IHC-Fr (formaldehyde-fixed frozen sections). Tissue samples were fixed with formaldehyde and blocked with 2% BSA for 30 minutes at 20°C. The sample was incubated with primary antibody (1/200 in PBS) at 4°C for 9 hours. An Alexa Fluor®488-conjugated Goat polyclonal to rabbit IgG (1/200) was used as secondary antibody. Nuclei were stained with DAPI.
This image is courtesy of an anonymous Abreview

ab39400 staining AMPK alpha 1 + AMPK alpha 2 in human 293ft cells by Immunocytochemistry/ Immunofluorescence. The cells were paraformaldehyde fixed, permeabilised in 0.1% Triton X-100 and then blocked using 5% serum for 1 hour at 25°C. Samples were then incubated with primary antibody at 1/100 for 2 hours at 25°C. The secondary antibody used was a goat anti-rabbit IgG conjugated to Alexa Fluor® 488 (green) used at a 1/250 dilution. DAPI was used to stain the cell nuclei (blue).
This image is courtesy of an anonymous abreview.

Blocking Step: 5% Milk for 2 hours at 25°C
This image is courtesy of an anonymous Abreview

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