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Recombinant Phospho-S6 Ribosomal Protein (Ser240, 244) Monoclonal Antibody (AN302078L)

Recombinant Phospho-S6 Ribosomal Protein (Ser240, 244) Monoclonal Antibody - 1
  • Recombinant Phospho-S6 Ribosomal Protein (Ser240, 244) Monoclonal Antibody - 1
  • Recombinant Phospho-S6 Ribosomal Protein (Ser240, 244) Monoclonal Antibody - 2
  • Recombinant Phospho-S6 Ribosomal Protein (Ser240, 244) Monoclonal Antibody - 3
  • +5
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: MCF-7
Verified Samples in IHC: Human breast cancer, Human colon, Mouse spleen, Rat kidney, Rat spleen
Verified Samples in IF: Hela
Verified Samples in IP: MCF-7+Serum starvation overnight, then grown in 20% FBS media for 30 minutes cells extracts
Dilution WB 1:500-1:1000,  IHC 1:500-1:1000,  IF 1:50,  IP 1:25-1:50
Isotype IgG, κ
Host Rabbit
Reactivity Human,  Rat,  Mouse
Applications WB,  IHC,  IF,  IP
Clonality Monoclonal;Recombinant
Immunogen phosphorylated human S6 Ribosomal Protein (Ser240/244) peptide
Abbre Phospho-S6 Ribosomal Protein (Ser240, 244)
Synonyms RPS,  OK/SW-cl,  RPS6,  S6,  OK/SW-cl.2
Swissprot
Calculated MW 29 kDa
Observed MW 32 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 Cytosol, Endoplasmic reticulum, Nucleus
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. A802
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background Component of the 40S small ribosomal subunit. Plays an important role in controlling cell growth and proliferation through the selective translation of particular classes of mRNA.
Other Clones

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Unconjugated

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