Facebook
Toll-free:1-888-852-8623

All categories

  • All categories
  • Flow Cytometry Antibodies
  • ELISA Kits
  • Magnetic Cell Sorting
  • Antibodies and Reagents
  • Apoptosis and Cell Health Detection
  • Metabolism Assays
  • Immunoassays
  • Cell Identification Kits
  • Proteins and Peptides
  • Cell Culture
Please enter the item number/product keyword!
Keyword cannot be empty !
INSERT SYMBOLS:
  • α
  • β
  • γ
  • δ
  • ε
  • ζ
  • η
  • θ
  • κ
  • μ
  • ω
  • σ
  • τ
  • λ
  • ⅩⅢ
  • ⅩⅢ
  • ⅩⅣ
  • ⅩⅤ
  • ⅩⅦ
  • ⅩⅧ
  • UP ↑

Recombinant Smooth Muscle Myosin heavy chain 11 Monoclonal Antibody (AN301659L)

Recombinant Smooth Muscle Myosin heavy chain 11 Monoclonal Antibody - 1
  • Recombinant Smooth Muscle Myosin heavy chain 11 Monoclonal Antibody - 1
  • Recombinant Smooth Muscle Myosin heavy chain 11 Monoclonal Antibody - 2
  • Recombinant Smooth Muscle Myosin heavy chain 11 Monoclonal Antibody - 3
All Size Price Qty
100μL $ 380.00
- +
50μL $ 249.00
- +
Add to cart

For research use only.

Verified Samples Verified Samples in WB: A375, A431
Verified Samples in IHC: Human colon, Human prostate hyperplasia
Dilution WB 1:500-1000,  IHC 1:200-1:1000
Isotype IgG, κ
Host Rabbit
Reactivity Human,  
Applications WB,  IHC
Clonality Monoclonal;Recombinant
Immunogen Recombinant human smooth muscle Myosin heavy chain 11 fragment
Abbre Smooth Muscle Myosin heavy chain 11
Synonyms FAA,  AAT,  MYH,  KIAA,  myosin,  MYH11,  AAT4,  FAA4,  SMHC,  SMMHC,  myosin-11,  KIAA0866
Swissprot
Calculated MW 227 kDa
Observed MW 280 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 Melanosome
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,  Cardiovascular
Clone No. A362
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping Ice bag
background The protein encoded by this gene is a smooth muscle myosin belonging to the myosin heavy chain family. The gene product is a subunit of a hexameric protein that consists of two heavy chain subunits and two pairs of non-identical light chain subunits. It functions as a major contractile protein, converting chemical energy into mechanical energy through the hydrolysis of ATP.
Other Clones

{{antibodyDetailsPage.numTotal}} Results

Other Formats

{{formatDetailsPage.numTotal}} Results

Unconjugated

  • IF:{{item.impact}}

    Journal:{{item.journal}} ({{item.year}})

    DOI:{{item.doi}}

    Reactivity:{{item.species}}

    Sample Type:{{item.organization}}

  • Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}}

Product Information