Actin Polyclonal Antibody (E-AB-30419)
For research use only.
| Verified Samples |
Verified Samples in WB: K562, Hela |
| Dilution | WB 1:500-1:2000, IHC 1:100-1:300 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Applications | WB, IHC-p |
| Clonality | Polyclonal |
| Immunogen | Synthesized peptide derived from the C-terminal region of human Actin |
| Abbre | Actin |
| Synonyms | ACTB, ACTBL3, ACTG, ACTG1, Actin, Beta-actin, FKSG30, Gamma-actin, Kappa-actin, POTE ankyrin domain family member K, POTEKP, Putative beta-actin-like protein 3, cytoplasmic 1, cytoplasmic 2 |
| Swissprot | |
| Calculated MW | 42 kDa |
| Observed MW |
45 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, actin cytoskeleton, cortical cytoskeleton, cytoskeleton, Cytosol, Extracellular region or secreted, blood microparticle, extracellular exosome, extracellular space, Nucleus, NuA4 histone acetyltransferase complex, nuclear chromatin, nucleoplasm, nucleus, Plasma Membrane, Other locations: cytoplasm, cytoplasmic ribonucleoprotein granule, dense body, focal adhesion, intracellular ribonucleoprotein complex, membrane, myelin sheath, protein complex, vesicle. |
| Concentration | 1 mg/mL |
| Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer, 0.5% protein protectant and 50% glycerol. |
| Purification Method | Affinity purification |
| Research Areas | Cancer, Signal Transduction, Tags and Cell Markers |
| Conjugation | Unconjugated |
| Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
| Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
| background | Actins are highly conserved proteins that are involved in various types of cell motility and are ubiquitously expressed in all eukaryotic cells. |
Other Clones
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Unconjugated
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