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100μL $ 130.00
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For research use only.

Verified Samples Verified Samples in WB: HeLa, MCF-7, HT-29, Hep G2, Mouse brain, Mouse kidney, Rat brain
Verified Samples in IF: U-2 OS
Dilution WB 1:2000-1:4000,  IF 1:200-1:400
Isotype IgG
Host Mouse
Reactivity Human,  Mouse,  Rat
Applications WB,  IF
Clonality Monoclonal
Immunogen Recombinant human TUBA1B protein by E.coli
Abbre alpha Tubulin
Synonyms Alpha tubulin 3,  Alpha-tubulin 3,  B alpha 1,  FLJ25113,  LIS3,  TBA1A,  TUBA1A,  TUBA3,  Tubulin alpha 1a,  Tubulin alpha 1A chain,  Tubulin alpha 3,  Tubulin alpha 3 chain,  Tubulin alpha brain specific,  Tubulin alpha-1A chain,  Tubulin alpha-3 chain,  Tubulin B alpha 1,  Tubulin B-alpha-1
Swissprot
Calculated MW 55 kDa
Observed MW 55 kDa

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 Cytoplasm, cytoskeleton 
Concentration 1 mg/mL
Buffer PBS with 0.05% proclin 300, 1% protective protein and 50% glycerol,pH7.4
Purification Method Protein A/G Purification
Research Areas Signal Transduction,  Neuroscience,  Tags and Cell Markers,  Isotype/Loading Controls,  Biochemicals,  Cancer,  Cardiovascular,  Cell Biology,  Developmental Biology,  Epigenetics and Nuclear Signaling,  Immunology,  Metabolism,  Microbiology,  Stem Cells
Clone No. 2H2
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 Tubulin is the major constituent of microtubules, a cylinder consisting of laterally associated linear protofilaments composed of alpha- and beta-tubulin heterodimers .Microtubules grow by the addition of GTP-tubulin dimers to the microtubule end, where a stabilizing cap forms.Below the cap, tubulin dimers are in GDP-bound state, owing to GTPase activity of alpha-tubulin.
Other Clones

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Unconjugated

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