RP2 Protein (Myc-DYKDDDDK Tag)

Produktnummer ABIN2731105

Produktdetails

Target: RP2 (Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2))

Protein-Typ: Recombinant

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses RP2 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human RP2 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: RP2 (Retinitis Pigmentosa 2 (X-Linked Recessive) (RP2))

Andere Bezeichnung: Rp2 (RP2 Produkte)

Synonyme: Rp2h Protein, RGD1565124 Protein, RP2 Protein, wu:fj10e02 Protein, wu:fm72d05 Protein, zfrp2 Protein, zgc:55632 Protein, DELXp11.3 Protein, NM23-H10 Protein, NME10 Protein, TBCCD2 Protein, XRP2 Protein, AI662636 Protein, Rp2 Protein, RP2, ARL3 GTPase activating protein Protein, XRP2 protein Protein, XRP2-like protein Protein, retinitis pigmentosa 2 (X-linked recessive) Protein, RP2, ARL3 GTPase activating protein S homeolog Protein, retinitis pigmentosa 2 homolog Protein, Rp2 Protein, RP2 Protein, Bm1_36735 Protein, PITG_13367 Protein, LOAG_11813 Protein, rp2 Protein, rp2.S Protein

Hintergrund: The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefore be due to the accumulation of incorrectly-folded photoreceptor or neuron-specific tubulin isoforms followed by progressive cell death

Molekulargewicht: 39.5 kDa

NCBI Accession: NP_008846

Pathways: Nucleotide Phosphorylation, Ribonucleoside Biosynthetic Process