TROP2/TACSTD2 Monoclonal Antibody (AN200176P)

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For research use only.
Verified Samples |
Verified Samples in WB:?MCF7, NCI-N87 Verified Samples in IHC: Human rectal cancer, Human placenta, Human mammary gland, monkey Palm skin, Human skin, Human hysterocarcinoma, Human skin cancer, Human thyroid cancer Verified Samples in IF: NCI-N87 Verified Samples in FCM: MCF-7, NCI-N87 |
Dilution | WB 1:500-1:2000, IHC-P 1:100-1:500, ICC/IF 1:20-1:100, FCM 1:25-1:100 |
Isotype | IgG1 |
Host | Mouse |
Reactivity | Human |
Applications | WB, IHC-P, FCM, ICC/IF |
Clonality | Monoclonal |
Immunogen | Recombinant Human TROP2 protein |
Abbre | TACSTD2 |
Synonyms | M1S, TROP, Cell surface glycoprotein Trop, Tumor-associated calcium signal transducer, Membrane component chromosome 1 surface marker, GA733, TACSTD, EGP, TACSTD2, EGP-1, EGP1, GA733-1, GA7331, GP50, M1S1, TROP2, Cell surface glycoprotein Trop-2, Membrane component chromosome 1 surface marker 1, Tumor-associated calcium signal transducer 2, TACD2, TROP-2 |
Swissprot | |
Calculated MW | 36 kDa |
Observed MW |
36-40 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. |
Tissue Specificity | Placenta, pancreatic carcinoma cell lines. |
Concentration | 1 mg/mL |
Buffer | 0.2 μm filtered solution in PBS |
Purification Method | Protein A |
Research Areas | Cancer |
Clone No. | 2C4 |
Conjugation | Unconjugated |
Storage | This antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles. |
Shipping | Ice bag |
background | This intronless gene encodes a carcinoma-associated antigen. This antigen is a cell surface receptor that transduces calcium signals. Mutations of this gene have been associated with gelatinous drop-like corneal dystrophy. |
Other Clones
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Other Formats
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Unconjugated
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