Suprabasin anticorps

N° du produit ABIN7882395

Cet anticorps Souris Monoclonal détecte spécifiquement Suprabasin dans IHC (p). Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour Suprabasin anticorps (ABIN7882395)

Antigène: Suprabasin (SBSN)

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp Suprabasin est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Classe de qualité: Carrier-free

Clone: SBSN-7964

Détail du produit anti-Suprabasin anticorps

Fonction: Suprabasin Antibody / SBSN (azide and preservative free)

Purification: Protein A/G affinity

Immunogène: A recombinant fragment of the human protein was used as the immunogen for the Suprabasin antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Suprabasin antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1 mg/mL in 1X PBS, BSA free, sodium azide free

Agent conservateur: Azide free

Stock: -20 °C

Stockage commentaire: Aliquot the Suprabasin antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur Suprabasin

Antigène: Suprabasin (SBSN)

Autre désignation: Suprabasin

Sujet: Suprabasin (SBSN) is a 247 amino acid secreted protein that is upregulated in differentiating keratinocytes and is though to play a role in epidermal differentiation. Expressed in uterus, skin, thymus and esophagus, suprabasin is encoded by a gene that maps to human chromosome 19q13.12. Chromosome 19 consists of about 63 million bases with over 1,400 genes, making up over 2 % of human genomic DNA. Chromosome 19 is the genetic home for a number of immunoglobulin superfamily members, including the killer cell and leukocyte Ig-like receptors, a number of ICAMs, the CEACAM and PSG families, and Fca receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and Insulin-dependent diabetes have been linked to chromosome 19.

UniProt: Q6UWP8