Promotional price valid on web orders only. Your contract pricing may differ. Interested in signing up for a dedicated account number?
Learn More

PCMT1 Mouse anti-Human, Clone: OTI2A9, Invitrogen™

Mouse Monoclonal Antibody

Manufacturer:  Invitrogen MA527236

Catalog No. PIMA527236


Add to cart

Description

Description

Three classes of protein carboxyl methyltransferases, distinguished by their methyl-acceptor substrate specificity, have been found in prokaryotic and eukaryotic cells. The type II enzyme catalyzes the transfer of a methyl group from S-adenosyl-L-methionine to the free carboxyl groups of D-aspartyl and L-isoaspartyl residues. These methyl-accepting residues result from the spontaneous deamidation, isomerization, and racemization of normal L-aspartyl and L-asparaginyl residues and represent sites of covalent damage to aging proteins PCMT1 (EC 2.1.1.77) is a protein repair enzyme that initiates the conversion of abnormal D-aspartyl and L-isoaspartyl residues to the normal L-aspartyl form.
Specifications

Specifications

PCMT1
Monoclonal
1 mg/mL
PBS with 1% BSA, 50% glycerol and 0.02% sodium azide; pH 7.3
P22061
PIMT, L-isoaspartyl protein carboxyl methyltransferase, protein L-isoaspartyl/D-aspartyl methyltransferase, protein-L-isoaspartate(D-aspartate) O-methyltransferase, protein-beta-aspartate methyltransferase
Mouse
IgG2b
100 μL
-20° C, Avoid Freeze/Thaw Cycles
Primary
5110
Immunohistochemistry (Paraffin), Western Blot
OTI2A9
Unconjugated
PCMT1
Liquid
PCMT1
Human recombit protein fragment corresponding to amino acids 60-285 of PCMT1 produced in E.coli
Affinity Chromatography
RUO
Antibody
Monoclonal
Human
Documents
Provide Content Correction

We continue to work to improve your shopping experience and your feedback regarding this content is very important to us. Please use the form below to provide feedback related to the content on this product.

Product Title

By clicking Submit, you acknowledge that you may be contacted by Fisher Scientific in regards to the feedback you have provided in this form. We will not share your information for any other purposes. All contact information provided shall also be maintained in accordance with our Privacy Policy.

Cancel Submit