LASS3 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2724513

Détail du produit

Antigène: LASS3 (CERS3) (Ceramide Synthase 3 (CERS3))

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette LASS3 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

• Recombinant human LASS3 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: LASS3 (CERS3) (Ceramide Synthase 3 (CERS3))

Autre désignation: Lass3 (CERS3 Produits)

Synonymes: F13B4.7 Protein, F13B4_7 Protein, LAG1 longevity assurance homolog 3 Protein, lass3 Protein, LASS3 Protein, ARCI9 Protein, 4930550L11Rik Protein, Gm488 Protein, Lass3 Protein, T3L Protein, RGD1564356 Protein, ceramide synthase 3 Protein, LAG1 longevity assurance-like protein Protein, ceramide synthase 3 S homeolog Protein, CERS3 Protein, LAG13 Protein, cers3.S Protein, Cers3 Protein

Sujet: This gene is a member of the ceramide synthase family of genes. The ceramide synthase enzymes regulate sphingolipid synthesis by catalyzing the formation of ceramides from sphingoid base and acyl-coA substrates. This family member is involved in the synthesis of ceramides with ultra-long-chain acyl moieties (ULC-Cers), important to the epidermis in its role in creating a protective barrier from the environment. The protein encoded by this gene has also been implicated in modification of the lipid structures required for spermatogenesis. Mutations in this gene have been associated with male fertility defects, and epidermal defects, including ichthyosis. Alternative splicing results in multiple transcript variants encoding different isoforms.

Poids moléculaire: 46.1 kDa

NCBI Accession: NP_849164