RP2 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2731105

Détail du produit

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

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette RP2 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

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

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

Information d'application

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

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

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

Stock: -80 °C

Stockage commentaire: 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.

Détail du antigène

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

Autre désignation: Rp2 (RP2 Produits)

Synonymes: 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

Sujet: 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

Poids moléculaire: 39.5 kDa

NCBI Accession: NP_008846

Pathways: Nucleotide Phosphorylation, Ribonucleoside Biosynthetic Process