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For research use only.

Verified Samples Verified Samples in WB: Human bladder
Verified Samples in IHC: Human cervical cancer, Human lung cancer
Dilution WB 1:500-1:2000,  IHC 1:30-1:150
Isotype IgG
Host Rabbit
Reactivity Human,  Mouse,  Rat
Applications WB,  IHC
Clonality Polyclonal
Immunogen Synthetic peptide of human MYL12B
Abbre MYL12B
Synonyms ML12B,  MLC 2A,  MLC-2,  MLC-2a,  MLC-B,  MLC20,  MRLC2,  MYL12B,  MYLC2B,  Myosin ,  Myosin light chain 12B regulatory,  Myosin regulatory light chain 12B,  Myosin regulatory light chain 2-B,  myosin regulatory light chain 2,  myosin regulatory light chain 2-B,  smooth muscle isoform
Swissprot
Calculated MW 20 kDa
Observed MW Refer to figures
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, myosin II complex, stress fiber, Cytosol, Extracellular region or secreted, extracellular exosome, Other locations: apical part of cell, brush border, cell cortex region, Z disc.
Concentration 0.5 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Antigen affinity purification
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 The activity of nonmuscle myosin II (see MYH9; MIM 160775) is regulated by phosphorylation of a regulatory light chain, such as MRLC2.This phosphorylation results in higher MgATPase activity and the assembly of myosin II filaments
Other Clones

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Other Formats

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Unconjugated

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