Anti-RASSF8 Antibody Picoband®

Ras association domain-containing protein 8 is a protein that in humans is encoded by the RASSF8 gene. This gene encodes a member of the Ras-assocation domain family (RASSF) of tumor suppressor proteins. This gene is essential for maintaining adherens junction function in epithelial cells and has a role in epithelial cell migration. It is a lung tumor suppressor gene candidate. A chromosomal translocation t (12;22) (p11.2; q13.3) leading to the fusion of this gene and the FBLN1 gene is found in a complex type of synpolydactyly. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Boster Bio Anti-RASSF8 Antibody Picoband® catalog # A11627-1. Tested in WB, IHC, ICC/IF, Flow Cytometry, ELISA applications. This antibody reacts with Human, Mouse. The brand Picoband indicates this is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications. Only our best-performing antibodies are designated as Picoband, ensuring unmatched performance.

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RASSF8

11228

Q8NHQ8

Human, Mouse

No cross reactivity with other proteins.

E.coli-derived human RASSF8 recombinant protein (Position: E50-V419) . Human RASSF8 shares 90.5% amino acid (aa) sequence identity with mouse RASSF8.

Expressed in all tissues.

WB, IHC, ICC, IF, Flow Cytometry, ELISA

Signal Transduction, Signaling Pathway, Small G Proteins

Immunogen affinity purified.

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

Lyophilized

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

Downstream effector of TOR signaling pathway involved in osmotic stress response. Could be involved in the control of plant growth and development. Phosphorylates the ribosomal proteins P14, P16 and S6. Functions as a repressor of cell proliferation and required for maintenance of chromosome stability and ploidy levels through the RBR1-E2F pathway.

1. Debeer, P., Schoenmakers, E. F. P. M., Twal, W. O., Argraves, W. S., De Smet, L., Fryns, J.-P., Van de Ven, W. J. M. The fibulin-1 gene (FBLN1) is disrupted in a t (12;22) associated with a complex type of synpolydactyly. J. Med. Genet. 39: 98-104, 2002. 2. Strausberg, R. L., Feingold, E. A., Grouse, L. H., Derge, J. G., Klausner, R. D., Collins, F. S., Wagner, L., Shenmen, C. M., Schuler, G. D., Altschul, S. F., Zeeberg, B., Buetow, K. H., and 71 others. Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. Proc. Nat. Acad. Sci. 99: 16899-16903, 2002.

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

https://www.bosterbio.com/msds?sku=A11627-1

52588 MW

48 kDa

6

Serine/threonine-protein kinase AtPK1/AtPK6

Cytoplasm. Nucleus.

Serine/threonine-protein kinase AtPK1/AtPK6

IgG

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