Suprabasin Antikörper

Produktnummer ABIN7882393

Der Maus Monoklonal anti-Suprabasin Antikörper wird verwendet zum Nachweis von Suprabasin in Proben von Human. Er wurde validiert für IHC (p).

Kurzübersicht für Suprabasin Antikörper (ABIN7882393)

Target: Suprabasin (SBSN)

Reaktivität: Human

Wirt: Maus

Klonalität: Monoklonal

Konjugat: Dieser Suprabasin Antikörper ist unkonjugiert

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

Güteklasse: Carrier-free

Klon: SBSN-7961

Produktdetails anti-Suprabasin Antikörper

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

Aufreinigung: Protein A/G affinity

Immunogen: A recombinant fragment from the human protein was used as the immunogen for the SBSN antibody.

Isotyp: IgG1, kappa

Anwendungsinformationen

Applikationshinweise: Optimal dilution of the SBSN antibody should be determined by the researcher.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 mg/mL

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

Konservierungsmittel: Azide free

Lagerung: -20 °C

Informationen zur Lagerung: Aliquot the SBSN antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Details zu Suprabasin

Target: Suprabasin (SBSN)

Andere Bezeichnung: SBSN

Hintergrund: 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