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Recombinant CTEN Monoclonal Antibody - 1
  • Recombinant CTEN Monoclonal Antibody - 1
  • Recombinant CTEN Monoclonal Antibody - 2
  • Recombinant CTEN Monoclonal Antibody - 3
  • +1
All Size Price Qty
100μL $ 380.00
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50μL $ 249.00
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For research use only.

Verified Samples Verified Samples in WB: HeLa
Verified Samples in IHC: Human liver, Rat liver
Verified Samples in IF: HepG2
Dilution WB 1:500-1:2000,  IHC 1:200-1:1000,  IF 1:50
Isotype IgG, κ
Host Rabbit
Reactivity Human,  Rat,  Mouse
Applications WB,  IHC,  IF
Clonality Monoclonal;Recombinant
Immunogen Recombinant human CTEN fragment
Abbre CTEN
Synonyms TNS,  tensin,  TNS4,  CTEN,  PP14434,  tensin-4,  C-terminal tensin-like protein
Swissprot
Calculated MW 76 kDa
Observed MW 90 kDa
The actual band is not consistent with the expectation.

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 Cytoskeleton
Concentration 1 mg/mL
Buffer PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
Purification Method Protein A purified
Research Areas Signal Transduction
Clone No. A201
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background May be involved in cell migration, cartilage development and in linking signal transduction pathways to the cytoskeleton. May promote apoptosis, via its cleavage by caspase-3.
Other Clones

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Unconjugated

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