RS1 antibody (AA 34-224)

Catalog No. ABIN7601377

The Rabbit Polyclonal anti-RS1 antibody is suitable to detect RS1 in samples from Human and Mouse. It has been validated for ELISA and WB.

Quick Overview for RS1 antibody (AA 34-224) (ABIN7601377)

Target: RS1 (Retinoschisin 1 (RS1))

Reactivity: Human, Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RS1 antibody is un-conjugated

Application: ELISA, Western Blotting (WB)

Product Details anti-RS1 Antibody

Binding Specificity: AA 34-224

Purpose: Anti-RS1 Antibody

Characteristics: 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.

Immunogen: 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

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Mouse
ELISA, 0.1-0.5 μg/mL, -

Restrictions: For Research Use only

Handling

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.

Storage: 4 °C,-20 °C

Storage Comment: 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.

Target Details for RS1

Target: RS1 (Retinoschisin 1 (RS1))

Alternative Name: RS1

Background: 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.

Molecular Weight: 25 kDa

Gene ID: 6247

UniProt: O15537