SVOPL Antikörper (AA 241-269)

Produktnummer ABIN1538165

Produktdetails anti-SVOPL Antikörper

Target: SVOPL (SVOP-Like (SVOPL))

Bindungsspezifität: AA 241-269

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SVOPL Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Aufreinigung: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This SVOPL antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 241-269 amino acids from the Central region of human SVOPL.

Klon: RB35924

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 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.

Lagerung: 4 °C,-20 °C

Informationen zur Lagerung: SVOPL Antibody (Center) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Haltbarkeit: 6 months

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.

Molekulargewicht: 53991

Gen-ID: 136306

NCBI Accession: NP_001132928, NP_777619

UniProt: Q8N434