SLC6A5 Antikörper (AA 1-200)

Produktnummer ABIN6148044

Produktdetails anti-SLC6A5 Antikörper

Target: SLC6A5 (Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5))

Bindungsspezifität: AA 1-200

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser SLC6A5 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: MDCSAPKEMN KLPANSPEAA AAQGHPDGPC APRTSPEQEL PAAAAPPPPR VPRSASTGAQ TFQSADARAC EAERPGVGSC KLSSPRAQAA SAALRDLREA QGAQASPPPG SSGPGNALHC KIPFLRGPEG DANVSVGKGT LERNNTPVVG WVNMSQSTVV LGTDGITSVL PGSVATVATQ EDEQGDENKA RGNWSSKLDF

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-200 of human SLC6A5 (NP_004202.3).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Kommentare:

HIGH QUALITY

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu SLC6A5

Target: SLC6A5 (Solute Carrier Family 6 (Neurotransmitter Transporter, Glycine), Member 5 (SLC6A5))

Andere Bezeichnung: SLC6A5 (SLC6A5 Produkte)

Synonyme: SLC6A5 antikoerper, Glyt2 antikoerper, prestin antikoerper, GLYT-2 antikoerper, GLYT2 antikoerper, HKPX3 antikoerper, NET1 antikoerper, solute carrier family 6 member 5 antikoerper, solute carrier family 6 (neurotransmitter transporter, glycine), member 5 antikoerper, SLC6A5 antikoerper, Slc6a5 antikoerper

Hintergrund: This gene encodes a sodium- and chloride-dependent glycine neurotransmitter transporter. This integral membrane glycoprotein is responsible for the clearance of extracellular glycine during glycine-mediated neurotransmission. This protein is found in glycinergic axons and maintains a high presynaptic pool of neurotransmitter at glycinergic synapses. Mutations in this gene cause hyperekplexia, a heterogenous neurological disorder characterized by exaggerated startle responses and neonatal apnea. Two transcript variants encoding different isoforms have been found for this gene.,SLC6A5,GLYT-2,GLYT2,HKPX3,NET1,Neuroscience,Cell Type Marker,Neuron marker,Synapse marker,SLC6A5

Molekulargewicht: 87 kDa

Gen-ID: 9152

UniProt: Q9Y345