ZG16 Polyclonal Antibody (E-AB-53054)
For research use only.
| Verified Samples |
Verified Samples in WB: Mouse pancreas, Mouse small intestines, Mouse large intestine, Human sigmoid Verified Samples in IHC: Human liver cancer, Human colorectal cancer |
| Dilution | WB 1:1000-1:5000, IHC 1:100-1:300 |
| Isotype | IgG |
| Host | Rabbit |
| Reactivity | Human, Mouse |
| Applications | WB, IHC |
| Clonality | Polyclonal |
| Immunogen | Fusion protein of human ZG16 |
| Abbre | ZG16 |
| Synonyms | JCLN, JCLN1, Jacalin like lectin domain containing, Secretory lectin ZG16, ZG16, ZG16A, Zg16, Zymogen granule membrane protein 16, Zymogen granule protein 16, Zymogen granule protein 16 homolog, hZG16 |
| Swissprot | |
| Calculated MW | 18 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 | Secreted>extracellular space>extracellular matrix. Cytoplasmic vesicle lumen. Golgi apparatus lumen. Stored in zymogen granules. |
| Concentration | 1.68 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 | May play a role in protein trafficking. May act as a linker molecule between the submembranous matrix on the luminal side of zymogen granule membrane (ZGM) and aggregated secretory proteins during granule formation in the TGN. |
Other Clones
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Unconjugated
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