Anti-PIP5K1B Antibody Picoband® fluoro647 Vervoeging

Predicted to enable 1-phosphatidylinositol-4-phosphate 5-kinase activity. Predicted to be involved in phosphatidylinositol phosphate biosynthetic process. Predicted to act upstream of or within phosphatidylinositol biosynthetic process. Located in uropod.

PIP5K1B; STM7; Phosphatidylinositol 4-phosphate 5-kinase type-1 beta; PIP5K1-beta; PtdIns (4P-5-kinase 1 beta; EC 2.7.1.68; Phosphatidylinositol 4-phosphate 5-kinase type I beta; PIP5KIbeta; Protein STM-7; Type I phosphatidylinositol 4-phosphate 5-kinase beta

PIP5K1B

8395

O14986

Human, Mouse, Rat

No cross-reactivity with other proteins

E.coli-derived human PIP5K1B recombinant protein (Position: R394-L540) . Human PIP5K1B shares 96.6% and 95.2% amino acid (aa) sequence identity with mouse and rat PIP5K1B, respectively.

Flow Cytometry

Immunogen affinity purified.

Liquid

1. Campuzano, V., Montermini, L., Molto, M. D., Pianese, L., Cossee, M., Cavalcanti, F., Monros, E., Rodius, F., Duclos, F., Monticelli, A., Zara, F., Canizares, J., and 15 others. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion. Science 271: 1423-1427, 1996. 2. Carvajal, J. J., Pook, M. A., dos Santos, M., Doudney, K., Hillermann, R., Minogue, S., Williamson, R., Hsuan, J. J., Chamberlain, S. The Friedreich's ataxia gene encodes a novel phosphatidylinositol-4-phosphate 5-kinase. Nature Genet. 14: 157-162, 1996. 3. Carvajal, J. J., Pook, M. A., Doudney, K., Hillermann, R., Wilkes, D., Al-Mahdawi, S., Williamson, R., Chamberlain, S. Friedreich's ataxia: a defect in signal transduction? Hum. Molec. Genet. 4: 1411-1419, 1995.

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

61 kDa

6

Phosphatidylinositol-4-phosphate 5-kinase type 1 beta

Phosphatidylinositol 4-phosphate 5-kinase type-1 beta

Rabbit IgG

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