RS1 anticorps (AA 34-224)

N° du produit ABIN7601377

L’anticorps Lapin Polyclonal anti-RS1 a été validé pour ELISA et WB. Il convient pour détecter RS1 dans des échantillons de Humain et Souris.

Aperçu rapide pour RS1 anticorps (AA 34-224) (ABIN7601377)

Antigène: RS1 (Retinoschisin 1 (RS1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp RS1 est non-conjugé

Application: ELISA, Western Blotting (WB)

Détail du produit anti-RS1 anticorps

Épitope: AA 34-224

Fonction: Anti-RS1 Antibody

Attributs du produit: Anti-RS1 Antibody (ABIN7601377). Tested in WB, ELISA applications. This antibody reacts with Human, Mouse. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human RS1 recombinant protein (Position: Y34-A224). Human RS1 shares 96.9% amino acid (aa) sequence identity with mouse RS1.

Isotype: IgG

Information d'application

Indications d'application: Western blot, 0.25-0.5 μg/mL, Mouse
ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Adding 0.2 mL of distilled water will yield a concentration of 500 μg/mL.

Concentration: 500 μg/mL

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

Stock: 4 °C,-20 °C

Stockage commentaire: 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.

Détails sur RS1

Antigène: RS1 (Retinoschisin 1 (RS1))

Autre désignation: RS1

Sujet: Retinoschisin also known as X-linked juvenile retinoschisis protein is a lectin that in humans is encoded by the RS1 gene. This gene encodes an extracellular protein that plays a crucial role in the cellular organization of the retina. The encoded protein is assembled and secreted from photoreceptors and bipolar cells as a homo-oligomeric protein complex. Mutations in this gene are responsible for X-linked retinoschisis, a common, early-onset macular degeneration in males that results in a splitting of the inner layers of the retina and severe loss in vision.

Poids moléculaire: 25 kDa

ID gène: 6247

UniProt: O15537