SVOPL Antikörper (Middle Region)

Produktnummer ABIN955017

Produktdetails anti-SVOPL Antikörper

Target: SVOPL (SVOP-Like (SVOPL))

Bindungsspezifität: AA 240-269, Middle Region

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SVOPL Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Enzyme Immunoassay (EIA)

Spezifität: This antibody detects SVOPL (Center).

Kreuzreaktivität (Details): Species reactivity (tested):Human

Aufreinigung: Protein A column followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide between 240-269 amino acids from the Central region of human SVOPL

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: Optimal working dilution should be determined by the investigator.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.25 mg/mL

Buffer: PBS, 0.09 % (W/V) sodium azide

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handhabung: Avoid repeated freezing and thawing.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung: Store at 2 - 8 °C for up to six months or (in aliquots) at -20 °C for longer.

Details zu SVOPL

Target: SVOPL (SVOP-Like (SVOPL))

Andere Bezeichnung: SVOPL (SVOPL Produkte)

Synonyme: zgc:101741 antikoerper, 9430071P14Rik antikoerper, SVOP like antikoerper, SVOP-like antikoerper, SV2 related protein homolog (rat)-like antikoerper, SVOPL antikoerper, svopl antikoerper, Svopl antikoerper

Hintergrund: SVOPL (putative transporter SVOPL), also known as SV2-related protein-like, is a 492 amino acid multi-pass membrane protein belonging to the major facilitator superfamily. SVOPL is a paralog to synaptic vesicle protein (SVOP) that exists as two alternatively spliced isoforms. The gene encoding SVOPL maps to human chromosome 7q34. Chromosome 7 is approximately 158 milllion bases long, encodes over 1,000 genes and makes up approximately 5 % of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. Deletions of portions of the q arm of chromosome 7 are linked to myeloid disorders, including acute myelogenous leukemia and myelodysplasia.Synonyms: Putative transporter

Molekulargewicht: Molecular Weight: 53991 Da

Gen-ID: 136306

NCBI Accession: NP_001132928