Anti-FYCO1 Antibody Picoband® PE Vervoeging

The gene encodes a Rab7 adapter protein that is implicated in the microtubule transport of autophagosomes. The encoded protein contains a RUN domain, a FYVE-type zinc finger domain, and Golgi dynamics (GOLD) domain. The encoded protein plays a role in microtubule plus end-directed transport of autophagic vesicles through interactions with the small GTPase Rab7, phosphatidylinositol-3-phosphate (PI3P), the autophagosome marker LC3, and the kinesin KIF5. Mutations in this gene are associated with inclusion body myositis (IBM) and autosomal recessive congenital cataracts (CATC2) .

FYCO1; ZFYVE7; FYVE and coiled-coil domain-containing protein 1; Zinc finger FYVE domain-containing protein 7

FYCO1

79443

Q9BQS8

Human, Mouse, Rat

No cross-reactivity with other proteins

E.coli-derived human FYCO1 recombinant protein (Position: M1-K1019) . Human FYCO1 shares 72.2% amino acid (aa) sequence identity with mouse FYCO1.

Flow Cytometry

Immunogen affinity purified.

Liquid

1. Chen, J., Ma, Z., Jiao, X., Fariss, R., Kantorow, W. L., Kantorow, M., Pras, E., Frydman, M., Pras, E., Riazuddin, S., Riazuddin, S. A., Hejtmancik, J. F. Mutations in FYCO1 cause autosomal-recessive congenital cataracts. Am. J. Hum. Genet. 88: 827-838, 2011. 2. Kiss, H., Yang, Y., Kiss, C., Andersson, K., Klein, G., Imreh, S., Dumanski, J. P. The transcriptional map of the common eliminated region 1 (C3CER1) in 3p21.3. Europ. J. Hum. Genet. 10: 52-61, 2002. 3. Pras, E., Pras, E., Bakhan, T., Levy-Nissenbaum, E., Lahat, H., Assia, E. I., Garzozi, H. J., Kastner, D. L., Goldman, B., Frydman, M. A gene causing autosomal recessive cataract maps to the short arm of chromosome 3. Isr. Med. Assoc. J. 3: 559-562, 2001.

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

167 kDa

6

FYVE and coiled-coil domain autophagy adaptor 1

FYVE and coiled-coil domain-containing protein 1

Rabbit IgG

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