Anti-MAGI2 Antibody Picoband®

SKU: A04546-2

Size: 100 μg

Storage: At -20℃ for one year from date of receipt. After reconstitution, at 4℃ for one month. It can also be aliquotted and stored frozen at -20℃ for six months. Avoid repeated freezing and thawing.

Form: Lyophilized

Reactivity: Human,Mouse,Rat

Applications: WB,Flow Cytometry,ELISA

Application Details: Western blot, 0.25-0.5 μg/ml, Mouse, Rat
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
ELISA, 0.1-0.5 μg/ml, -

Gene Name: MAGI2

Specificity:

Background: Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2 also known as membrane-associated guanylate kinase inverted 2 (MAGI-2) and atrophin-1-interacting protein 1 (AIP-1) is an enzyme that in humans is encoded by the MAGI2 gene. The protein encoded by this gene interacts with atrophin-1. Atrophin-1 contains a polyglutamine repeat, expansion of which is responsible for dentatorubral and pallidoluysian atrophy. This encoded protein is characterized by two WW domains, a guanylate kinase-like domain, and multiple PDZ domains. It has structural similarity to the membrane-associated guanylate kinase homologue (MAGUK) family.

Immunogen: E.coli-derived human MAGI2 recombinant protein (Position: Q40-P1140). Human MAGI2 shares 97.5% and 96.8% amino acid (aa) sequence identity with mouse and rat MAGI2, respectively.

Clonality: Polyclonal

Contents: Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.

Purification: Immunogen affinity purified.

Reconstitution: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.

Reference: 1. Balbas, M. D., Burgess, M. R., Murali, R., Wongvipat, J., Skaggs, B. J., Mundel, P., Weins, A., Sawyers, C. L. MAFI-2 scaffold protein is critical for kidney barrier function. Proc. Nat. Acad. Sci. 111: 14876-14881, 2014. 2. Bauss, K., Knapp, B., Jores, P., Roepman, R., Kremer, H., v. Wijk, E., Marker, T., Wolfrum, U. Phosphorylation of the Usher syndrome 1G protein SANS controls Magi2-mediated endocytosis. Hum. Molec. Genet. 23: 3923-3942, 2014. 3. Bierzynska, A., Soderquest, K., Dean, P., Colby, E., Rollason, R., Jones, C., Inward, C. D., McCarthy, H. J., Simpson, M. A., Lord, G. M., Williams, M., Welsh, G. I., Koziell, A. B., Saleem, M. A., NephrosS, the UK study of Nephrotic Syndrome. MAGI2 mutations cause congenital nephrotic syndrome. J. Am. Soc. Nephrol. 28: 1614-1621, 2017.

Uniprot ID: Q86UL8

Host: Rabbit

Concentration: Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.

Conjugate:

Cross Reactivity:

Isotype: IgG

Phospho_site:

Clone Number:

Observed Molecular Weight: 159 kDa

Calculated Molecular Weight: 140 kDa

Gene ID: 9863

Protein Name: Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2

Gene Full Name: membrane associated guanylate kinase, WW and PDZ domain containing 2

Synonyms: MAGI2; ACVRINP1; AIP1; KIAA0705; Membrane-associated guanylate kinase, WW and PDZ domain-containing protein 2; Atrophin-1-interacting protein 1; AIP-1; Atrophin-1-interacting protein A; Membrane-associated guanylate kinase inverted 2; MAGI-2