SLC6A2 Antilichaam

This gene encodes a member of the sodium:neurotransmitter symporter family. This member is a multi-pass membrane protein, which is responsible for reuptake of norepinephrine into presynaptic nerve terminals and is a regulator of norepinephrine homeostasis. Mutations in this gene cause orthostatic intolerance, a syndrome characterized by lightheadedness, fatigue, altered mentation and syncope. Alternatively spliced transcript variants encoding different isoforms have been identified in this gene.

6530

P23975

Human, Mouse, Rat

Recombinant fusion protein containing a sequence corresponding to amino acids 1-70 of human SLC6A2 (NP_001165975.1) .

Unconjugated

Primary Antibodies

Neuroscience

Affinity purification

A-549

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 69kDa

IgG

WB: 1:500 - 1:2000

SLC6A2

SH-SY5Y

Mouse kidney

Mouse spinal cord

Solute carrier family 6 (neurotransmitter transporter), member 2

Homo sapiens

SLC6A2, NAT1, NET, NET1, SLC6A5

WB

Liquid