Welcome to GenPrice! Check out our latest updates.

Shopping Cart (0)

Your cart is empty

Add some products to get started!

Anti-POMGNT1 Antibody Picoband® Fluoro488 Conjugated

Product Specifications

Background

Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 is an enzyme that in humans is encoded by the POMGNT1 gene. This gene encodes a type II transmembrane protein that resides in the Golgi apparatus. It participates in O-mannosyl glycosylation and is specific for alpha linked terminal mannose. Mutations in this gene may be associated with muscle-eye-brain disease and several congenital muscular dystrophies. Alternatively spliced transcript variants that encode different protein isoforms have been described.

Gene Name

POMGNT1

Gene ID

55624

UniProt

Q8WZA1

Host

Rabbit

Reactivity

Human, Mouse, Rat

Immunogen

E.coli-derived human POMGNT1 recombinant protein (Position: R96-E394) . Human POMGNT1 shares 99.7% amino acid (aa) sequence identity with both mouse and rat POMGNT1.

Clonality

Polyclonal

Applications

Flow Cytometry

Purification

Immunogen affinity purified.

Form

Liquid

References & Citations

1. Biancheri, R., Bertini, E., Falace, A., Pedemonte, M., Rossi, A., D'Amico, A., Scapolan, S., Bergamino, L., Petrini, S., Cassandrini, D., Broda, P., Manfredi, M., Zara, F., Santorelli, F. M., Minetti, C., Bruno, C. POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum. Arch. Neurol. 63: 1491-1495, 2006. 2. Bouchet, C., Gonzales, M., Vuillaumier-Barrot, S., Devisme, L., Lebizec, C., Alanio, E., Bazin, A., Bessieres-Grattagliano, B., Bigi, N., Blanchet, P., Bonneau, D., Bonnieres, M., and 22 others. Molecular heterogeneity in fetal forms of type II lissencephaly. Hum. Mutat. 28: 1020-1027, 2007. 3. Clement, E. M., Godfrey, C., Tan, J., Brockington, M., Torelli, S., Feng, L., Brown, S. C., Jimenez-Mallebrera, C., Sewry, C. A., Longman, C., Mein, R., Abbs, S., Vajsar, J., Schachter, H., Muntoni, F. Mild POMGnT1 mutations underlie a novel limb-girdle muscular dystrophy variant. Arch. Neurol. 65: 137-141, 2008.

Storage Conditions

At -20 ̊C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Applications Notes

6

Isotype

IgG

Contents

Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.

Curated Selection

Explore Other Products

Discover premium biology products from our extensive collection of 20M+ items

Di-tert-Butyl octane-1,8-diyldicarbamate
OR1038813-01 5 g

Di-tert-Butyl octane-1,8-diyldicarbamate

Ask
View Details
Di-tert-Butyl octane-1,8-diyldicarbamate
OR1038813-02 10 g

Di-tert-Butyl octane-1,8-diyldicarbamate

Ask
View Details
D-Aspartate Oxidase (DDO) Antibody (Biotin)
abx315668-01 20 µg

D-Aspartate Oxidase (DDO) Antibody (Biotin)

Ask
View Details
D-Aspartate Oxidase (DDO) Antibody (Biotin)
abx315668-02 50 µg

D-Aspartate Oxidase (DDO) Antibody (Biotin)

Ask
View Details
D-Aspartate Oxidase (DDO) Antibody (Biotin)
abx315668-03 100 µg

D-Aspartate Oxidase (DDO) Antibody (Biotin)

Ask
View Details
D-Aspartate Oxidase (DDO) Antibody (Biotin)
abx315668-04 200 µg

D-Aspartate Oxidase (DDO) Antibody (Biotin)

Ask
View Details