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Reactivity | HuSpecies Glossary |
Applications | WB, ELISA, Func, PA, AP |
Description | A recombinant protein with a N-terminal GST tag corresponding to the amino acid sequence 1-62 of Human PCP4 Source: Wheat Germ (in vitro) Amino Acid Sequence: MSERQGAGATNGKDKTSGENDGQKKVQEEFDIDMDAPETERAAVAIQSQFRKFQKKKAGSQS |
Preparation Method |
in vitro wheat germ expression system |
Details of Functionality | This protein was produced in an in vitro wheat germ expression system that should preserve correct conformational folding that is necessary for biological function. While it is possible that this protein could display some level of activity, the functionality of this protein has not been explicitly measured or validated. |
Source | Wheat germ |
Protein/Peptide Type | Partial Recombinant Protein |
Gene | PCP4 |
Purity | >80% by SDS-PAGE and Coomassie blue staining |
Dilutions |
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Theoretical MW | 32.56 kDa. Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors. |
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Publications |
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Storage | Store at -80C. Avoid freeze-thaw cycles. |
Buffer | 50 mM Tris-HCI, 10 mM reduced Glutathione, pH 8.0 in the elution buffer. |
Preservative | No Preservative |
Purity | >80% by SDS-PAGE and Coomassie blue staining |
Publication using H00005121-Q01 | Applications | Species |
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Ichikawa H, Terayama R, Yamaai T et al. Peptide 19 in the rat superior cervical ganglion. Neuroscience. 2009 Mar 19. [PMID: 19303431] |
Diseases for PCP4 Partial Recombinant Protein (H00005121-Q01)Discover more about diseases related to PCP4 Partial Recombinant Protein (H00005121-Q01).
| Pathways for PCP4 Partial Recombinant Protein (H00005121-Q01)View related products by pathway.
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PTMs for PCP4 Partial Recombinant Protein (H00005121-Q01)Learn more about PTMs related to PCP4 Partial Recombinant Protein (H00005121-Q01).
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RNA-binding protein Staufen1 conspires with Atxn2 in stress granules to cause neurodegeneration by dysregulating RNA metabolism By Jamshed Arslan Pharm.D. Spinocerebellar ataxia type 2 (SCA2) is a movement disorder characterized by neurodegeneration. The cause of this autosomal dominant disease is a mutation in the RNA processing gene Atxn2,... Read full blog post. |
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Gene Symbol | PCP4 |