SMS antibody (AA 102-365)

Catalog No. ABIN7599638

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

Quick Overview for SMS antibody (AA 102-365) (ABIN7599638)

Target: SMS (Spermine Synthase, SMS (SMS))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This SMS antibody is un-conjugated

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS)

Product Details anti-SMS Antibody

Binding Specificity: AA 102-365

Purpose: Anti-Spermine synthase/SMS Antibody

Cross-Reactivity (Details): No cross-reactivity with other proteins.

Characteristics: Anti-Spermine synthase/SMS Antibody (ABIN7599638). Tested in ELISA, Flow Cytometry, WB applications. This antibody reacts with Human. 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 Spermine synthase/SMS recombinant protein (Position: Q102-K365).

Isotype: IgG

Application Details

Application Notes: Western blot, 0.25-0.5 μg/mL, Human
Flow Cytometry (Fixed), 1-3 μg/1x10⁶ cells, Human
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 SMS

Target: SMS (Spermine Synthase, SMS (SMS))

Alternative Name: SMS

Background:

Synonyms: Beta-galactosidase, Glb1, Glb1_mapped, rCG_25043

Background: This gene encodes a protein belonging to the spermidine/spermin synthase family and catalyzes the production of spermine from spermidine. Pseudogenes of this gene are located on chromosomes 1, 5, 6 and X. Mutations in this gene cause an X-linked intellectual disability called Snyder-Robinson Syndrome (SRS). Multiple transcript variants encoding different isoforms have been found for this gene.

Molecular Weight: 41 kDa

Gene ID: 6611

UniProt: P52788