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Recombinant Phospho-TBK1 (Ser172) Monoclonal Antibody (AN301141L)

Recombinant Phospho-TBK1 (Ser172) Monoclonal Antibody - 1
  • Recombinant Phospho-TBK1 (Ser172) Monoclonal Antibody - 1
  • Recombinant Phospho-TBK1 (Ser172) Monoclonal Antibody - 2
All Size Price Qty
100μL $ 320.00
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50μL $ 211.00
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For research use only.

Verified Samples Verified Samples in WB: Hela
Dilution WB 1:2000-1:10000,  
Isotype IgG,κ
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB
Clonality Monoclonal;Recombinant
Immunogen A synthetic peptide corresponding to residues around (Ser172) of Human Phospho-TBK1
Abbre TBK1
Synonyms TBK,  FTDALS,  TBK1,  FTDALS4,  NAK,  T2K
Swissprot
Calculated MW 84 kDa
Observed MW 84 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 Cytoplasm, Upon mitogen stimulation or triggering of the immune system, TBK1 is recruited to the exocyst by EXOC2.
Concentration 0.2 mg/mL
Buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification Method Protein A
Research Areas Signal Transduction,  Epigenetics and Nuclear Signaling
Clone No. 6H2
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background The NF-kappa-B (NFKB) complex of proteins is inhibited by I-kappa-B (IKB) proteins, which inactivate NFKB by trapping it in the cytoplasm. Phosphorylation of serine residues on the IKB proteins by IKB kinases marks them for destruction via the ubiquitination pathway, thereby allowing activation and nuclear translocation of the NFKB complex. The protein encoded by this gene is similar to IKB kinases and can mediate NFKB activation in response to certain growth factors.
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Unconjugated

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