Recombinant Glyt2 Monoklonale Antilichaam

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.

Glyt2

Q9Y345

Human; Mouse; Rat

Recombinant Human Glyt2 protein

NET; HKPX; SLC6A; SLC6A5; GLYT-2; GLYT2; HKPX3; NET1

5B13

Unconjugated

WB

Neuroscience

Protein A

0.2 mg/mL

WB 1:1000-1:5000

PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.

Ice bag

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

https://789.bio/eb/frXpoQY6

88 kDa

88 kDa

IgG, κ