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100μL $ 260.00
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For research use only.

Verified Samples Verified Samples in WB: Mouse liver
Verified Samples in IHC: Mouse liver
Verified Samples in IF: HepG2
Dilution WB 1:1000-1:2000,  IHC 1:100-1:200,  IF 1:100-1:400
Isotype IgG
Host Rabbit
Reactivity Human,  Mouse
Applications WB,  IHC,  IF
Clonality Polyclonal
Immunogen Recombinant Mouse Glucokinase protein
Abbre GCK
Synonyms ATP:D-hexose 6-phosphotransferase,  FGQTL3,  GCK,  GK,  GLK,  Glucokinase,  HHF3,  HK IV,  HK4,  HKIV,  HXK4,  HXKP,  Hexokinase D pancreatic isozyme,  Hexokinase type IV,  Hexokinase-4,  Hexokinase-D,  LGLK,  MODY2
Swissprot
Calculated MW 52 kDa
Observed MW 52 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.

Cellular Localization Nucleus. Cytoplasm.
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,  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 Hexokinases phosphorylate glucose to produce glucose-6-phosphate, the first step in most glucose metabolism pathways. Alternative splicing of this gene results in three tissue-specific forms of glucokinase, one found in pancreatic islet beta cells and two found in liver. The protein localizes to the outer membrane of mitochondria. In contrast to other forms of hexokinase, this enzyme is not inhibited by its product glucose-6-phosphate but remains active while glucose is abundant. Mutations in this gene have been associated with non-insulin dependent diabetes mellitus (NIDDM), maturity onset diabetes of the young, type 2 (MODY2) and persistent hyperinsulinemic hypoglycemia of infancy (PHHI).
Other Clones

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Unconjugated

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