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Recombinant eEF1G Monoclonal Antibody - 1
  • Recombinant eEF1G Monoclonal Antibody - 1
  • Recombinant eEF1G Monoclonal Antibody - 2
  • Recombinant eEF1G Monoclonal Antibody - 3
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100μL $ 380.00
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50μL $ 249.00
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For research use only.

Verified Samples Verified Samples in WB: HT-29, F9, Panc-1, C6
Verified Samples in IHC: Human placenta, Mouse brain, Rat brain
Dilution WB 1:1000-1:5000,  IHC 1:50-1:100
Isotype IgG, κ
Host Rabbit
Reactivity Human,  Rat,  Mouse
Applications WB,  IHC
Clonality Monoclonal;Recombinant
Immunogen Recombinant human eEF1G fragment
Abbre eEF1G
Synonyms GIG,  PRO,  EEF1G,  EF1G,  GIG35,  PRO1608,  2610301D06Rik,  AA407312,  eEF 1B gamma,  EEF 1G,  eEF-1B gamma,  EF 1 gamma,  EF 1G,  EF1 gamma,  EF-1-gamma,  Elongation factor 1 gamma,  Elongation factor 1-gamma,  Eukaryotic translation elongation factor 1 gamma,  GIG 35,  MGC103354,  MGC114210,  MGC144723,  MGC144724,  MGC94929,  Pancreatic tumor related protein,  Translation elongation factor eEF 1 gamma chain
Swissprot
Calculated MW 50 kDa
Observed MW 50 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 Extracellular region, Nucleus, cytoplasm, membrane
Concentration 1 mg/mL
Buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification Method Protein A purified
Research Areas Epigenetics and Nuclear Signaling
Clone No. A209
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background Probably plays a role in anchoring the complex to other cellular components.
Other Clones

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Other Formats

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Unconjugated

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