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100μL $ 260.00
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For research use only.

Verified Samples Verified Samples in WB: Human Hep G2, Human Hela, Mouse NIH/3T3
Verified Samples in IHC: Human breast
Verified Samples in IF: Human MCF7
Dilution WB 1:500-1:1000,  IHC 1:100-1:200,  IF 1:100-1:400
Isotype IgG
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC,  IF
Clonality Polyclonal
Immunogen Recombinant Rat Ampk2 protein expressed by E.coli
Abbre AMPK
Synonyms 5'-AMP-activated protein kinase catalytic subunit alpha-2,  AAPK2,  ACACA kinase,  AMPK alpha 2 chain,  AMPK subunit alpha-2,  AMPK2,  AMPKa2,  AMPKalpha2,  Acetyl-CoA carboxylase kinase,  HMGCR kinase,  Hydroxymethylglutaryl-CoA reductase kinase,  PRKAA,  PRKAA2,  Protein kinase
Swissprot
Calculated MW 62 kDa
Observed MW 62 kDa

Western blotting is a method for detecting a certain protein in a complex sample based on the specific binding of antigen and antibody. Different proteins can be divided into bands based on different mobility rates. The mobility is affected by many factors, which may cause the observed band size to be inconsistent with the expected size. The common factors include:

1. Post-translational modifications: For example, modifications such as glycosylation, phosphorylation, methylation, and acetylation will increase the molecular weight of the protein.

2. Splicing variants: Different expression patterns of various mRNA splicing bodies may produce proteins of different sizes.

3. Post-translational cleavage: Many proteins are first synthesized into precursor proteins and then cleaved to form active forms, such as COL1A1.

4. Relative charge: the composition of amino acids (the proportion of charged amino acids and uncharged amino acids).

5. Formation of multimers: For example, in protein dimer, strong interactions between proteins can cause the bands to be larger. However, the use of reducing conditions can usually avoid the formation of multimers.

If a protein in a sample has different modified forms at the same time, multiple bands may be detected on the membrane.

Concentration 1 mg/mL
Buffer PBS with 0.05% proclin 300, 1% protective protein and 50% glycerol,pH7.4
Purification Method Antigen Affinity Purification
Research Areas Cancer,  Cardiovascular,  Metabolism,  Signal Transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
background The protein encoded by this gene is a catalytic subunit of the AMP-activated protein kinase (AMPK). AMPK is a heterotrimer consisting of an alpha catalytic subunit, and non-catalytic beta and gamma subunits. AMPK is an important energy-sensing enzyme that monitors cellular energy status. In response to cellular metabolic stresses, AMPK is activated, and thus phosphorylates and inactivates acetyl-CoA carboxylase (ACC) and beta-hydroxy beta-methylglutaryl-CoA reductase (HMGCR), key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. Studies of the mouse counterpart suggest that this catalytic subunit may control whole-body insulin sensitivity and is necessary for maintaining myocardial energy homeostasis during ischemia.
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Unconjugated

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