Recombinant Ki67 Monoclonal Antibody (AN301074L)

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For research use only.
Verified Samples |
Verified Samples in WB: Hela Verified Samples in IHC: Human appendix tissue, Mouse colon tissue, Rat spleen |
Dilution | IHC 1:200-1000, WB 1:1000-5000 |
Isotype | IgG,κ |
Host | Rabbit |
Reactivity | Human, Mouse, Rat |
Applications | WB, IHC |
Clonality | Monoclonal;Recombinant |
Immunogen | Recombinant Human Ki67 protein |
Abbre | Ki67 |
Synonyms | MIB, MKI, marker of proliferation Ki, Proliferation marker protein Ki, Antigen identified by monoclonal antibody Ki, PPP1R, MKI67, KIA, MIB-, MIB-1, PPP1R105, marker of proliferation Ki-67, Ki67, Antigen identified by monoclonal antibody Ki-67, Antigen Ki67, Antigen KI-67, Proliferation marker protein Ki-67, Antigen identified by monoclonal Ki 67, Antigen identified by monoclonal Ki-67, MIB 1, Proliferation related Ki 67 antigen, Protein phosphatase 1 regulatory subunit 105, RP11-380J17.2, Ki-67 |
Swissprot | |
Calculated MW | 359 kDa |
Observed MW |
359 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 | Nucleus |
Concentration | 0.2 mg/mL |
Buffer | PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant. |
Purification Method | Protein A |
Research Areas | Cell Biology, Neuroscience, Tags & Cell Markers, Cancer |
Clone No. | 1F14 |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | Ice bag |
background | This gene encodes a nuclear protein that is associated with and may be necessary for cellular proliferation. Alternatively spliced transcript variants have been described. A related pseudogene exists on chromosome X. |
Other Clones
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Unconjugated
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