
Anti-RPGRIP1L Antibody Picoband® fluoro647 Vervoeging
Kwaliteit
ISO Gecertificeerd
Levering
24-48 uur
Technische Specificaties
The protein encoded by this gene can localize to the basal body-centrosome complex or to primary cilia and centrosomes in ciliated cells. The encoded protein has been found to interact with nephrocystin-4. Defects in this gene are a cause of Joubert syndrome type 7 (JBTS7) and Meckel syndrome type 5 (MKS5) .
Endothelial cell-specific molecule 1; ESM-1; ESM1
RPGRIP1L
23322
Q68CZ1
• Rabbit
Human, Mouse, Rat
No cross-reactivity with other proteins.
E.coli-derived human RPGRIP1L recombinant protein (Position: E608-D1264) .
• Polyclonal
Expressed in lung, on the vascular capillary network within alveolar walls, and also at lower level in kidney.
Flow Cytometry
Cell Type Markers, Tags & Cell Markers
Immunogen affinity purified.
Liquid
Involved in angiogenesis; promotes angiogenic sprouting. May have potent implications in lung endothelial cell-leukocyte interactions.
1. Arts, H. H., Doherty, D., van Beersum, S. E. C., Parisi, M. A., Letteboer, S. J. F., Gorden, N. T., Peters, T. A., Marker, T., Voesenek, K., Kartono, A., Ozyurek, H., Farin, F. M., Kroes, H. Y., Wolfrum, U., Brunner, H. G., Cremers, F. P. M., Glass, I. A., Knoers, N. V. A. M., Roepman, R. Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome. Nature Genet. 39: 882-888, 2007. 2. Brancati, F., Travaglini, L., Zablocka, D., Boltshauser, E., Accorsi, P., Montagna, G., Silhavy, J. L., Barrano, G., Bertini, E., Emma, F., Rigoli, L., the International JSRD Study Group, Dallapiccola, B., Gleeson, J. G., Valente, E. M. RPGRIP1L mutations are mainly associated with the cerebello-renal phenotype of Joubert syndrome-related disorders. Clin. Genet. 74: 164-170, 2008. 3. Delous, M., Baala, L., Salomon, R., Laclef, C., Vierkotten, J., Tory, K., Golzio, C., Lacoste, T., Besse, L., Ozilou, C., Moutkine, I., Hellman, N. E., and 25 others. The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome. Nature Genet. 39: 875-881, 2007.
At -20 ̊C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.
6
Endothelial cell specific molecule 1
Secreted.
Rabbit IgG
Each vial contains 50% glycerol, 0.9% NaCl, 0.2% Na2HPO4, 0.02% NaN3.
Beschrijving
Anti-RPGRIP1L Antibody Picoband® fluoro647 Vervoeging Beschikbaar in 100 µg/Vial. Bestel eenvoudig online met snelle levering.
Specificaties
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