Measured by its ability to cleave a colorimetric peptide substrate, Hippuryl-Arg. The specific activity is >5,000 pmol/min/µg, as measured under the described conditions.
Source
Mouse myeloma cell line, NS0-derived mouse Carboxypeptidase B1/CPB1 protein Ser16-Tyr415, with a C-terminal 10-His tag Accession # NP_083982
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Note
<1.0 EU per 1 μg of the protein by the LAL method.
Applications/Dilutions
Dilutions
Enzyme Activity
Theoretical MW
47 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.
Substrate: Hippuryl-Arg (Sigma, Catalog # H-2508), 25 mM in diH2O
96-well Clear UV Plate (Corning, Catalog # 3635)
Plate Reader (Model: SpectraMax Plus by Molecular Devices) or equivalent
Activate rmCPB1 at 100 µg/mL with 1 µg/mL Trypsin in Activation Buffer.
Incubate at room temperature for 30 minutes.
Add AEBSF at a final concentration of 1 mM to stop reaction.
Dilute activated rmCPB1 to 2 µg/mL in Assay Buffer.
Dilute Substrate to 2 mM in Assay Buffer.
In a plate, load 50 µL of 2 µg/mL rmCPB1, and include a Substrate Blank containing 50 µL Assay Buffer.
Start the reaction by adding 50 µL of 2 mM Substrate into wells.
Read in kinetic mode for 5 minutes at an absorbance of 254 nm.
Calculate specific activity using the following formula:
Specific Activity (pmol/min/µg) =
Adjusted Vmax* (OD/min) x Conversion Factor** (pmol/OD)
amount of enzyme (µg)
*Adjusted for Substrate Blank **Derived using calibration standard Hippuric acid (Sigma Catalog # 112003).
Per Well:
rmCPB1: 0.1 µg
Substrate: 1 mM
Notes
This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.
Alternate Names for Recombinant Mouse Carboxypeptidase B1/CPB1 Protein, CF
carboxypeptidase B
carboxypeptidase B1 (tissue)
Carboxypeptidase B1
CPB
CPB1
DKFZp779K1333
EC 3.4.17
EC 3.4.17.2
Pancreas-specific protein
PASP
PCPB
procarboxypeptidase B
Background
Carboxypeptidase B1, encoded by the CPB1 gene, specifically cleaves the C-terminal Arg and Lys residues with a preference for Arg (1). The deduced amino acid sequence of mouse CPB1 consists of a signal peptide (residues 1 to 15), a pro region (residue 16 to 108), and a mature chain (residues 109 to 415). The purified rmCPB1 corresponds to the pro form, which can be activated by trypsin, the only pancreatic protease capable of generating active enzyme from the zymogen in vitro (1).
Aviles, F.X. and J. Vendrell (2004) in Handbook of Proteolytic Enzymes (ed. Barrett, et al.) pp. 831, Academic Press, San Diego.
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FAQs for Carboxypeptidase B1/CPB1 (2898-ZN). (Showing 1 - 2 of 2 FAQ).
I use porcine carboxypeptidase B (CPB) in my fermentation process. I want to detect the residual CPB in my finished product preferably by ELISA/western blot. How will antibody pairs from Novus Biologics help me do that? Is a colorimetric assay possible with the antibody pair?
Any detection system can be employed when using the antibody pairs. The detection system will depend on the secondary used against the detection primary antibody from the pair, and the conjugate on the secondary antibody. The pair will work effectively in capturing the protein of interest, and subsequently detecting it with the second antibody in the pair for ELISA. This pair is not evaluated in Western Blot directly, but there Novus carries similar primary antibodies that we have that are validated in that application.
I am trying to establish ELISA detection for carboxy peptidase. I am using a rat recombinant carboxypeptodase b from Roche diagnostics (cat no.03358682103). Can you please suggest the suitable kit .
Here is a link to our CPB1 products. H00001360-AP21 and H00001360-AP11 may suit your needs.
The concentration calculator allows you to quickly calculate the volume, mass or concentration of your vial. Simply enter your mass, volume, or concentration values for your reagent and the calculator will determine the rest.
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