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Anti-SLC1A1 / EAAT3 Antibody (aa510-523) LS-C152890

Note: This antibody replaces LS-C15445
Catalog Size Price
LS-C152890-100 100 µg (1 mg/ml) Unavailable

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100% Guaranteed
Mouse Monoclonal (IgG1) to Rat SLC1A1 / EAAT3
Rat, Mouse
IHC, Western blot


Rat SLC1A1 / EAAT3
Rat, Mouse (tested or 100% immunogen sequence identity)
Human, Monkey, Bovine, Dog, Guinea pig, Hamster, Horse, Rabbit, Chicken (at least 90% immunogen sequence identity)
IgG1 Monoclonal


  • IHC
  • Western blot (1 - 2 µg/ml)

Specificity and Use

SLC1A1 / EAAT3 antibody was raised against c-terminus peptide (KDKSDTISFTQTSQF) Percent identity by BLAST analysis: Human, Chimpanzee, Gorilla, Orangutan, Monkey, Galago, Marmoset, Mouse, Rat, Dog, Bovine, Hamster, Panda, Horse, Rabbit, Opossum, Guinea pig, Turkey, Zebra finch, Chicken, Lizard (93%); Elephant, Pig, Platypus, Xenopus (87%); Bat, Pufferfish, Zebrafish (80%).
Glutamate Transporter EAAC1. Based on protein sequence the antibody is expected to react with mouse, bovine and rabbit
Western blot: 1-2 ug/ml. Immunohistochemistry: 1-2 ug/ml. Optimal working dilutions must be determined by end user. EAAC1 is approximately 66-70kD; the protein can form homomultimers during preparation as well, thus often times large 200-220kD bands can a


0.02 M phosphate buffer, pH 7.6, 0.25 M sodium chloride, 0.1% sodium azide
stable 4°C
For research use only.

About SLC1A1 / EAAT3

P43005 NM_004170 NP_004161.4

SLC1A1 Antibody, EAAC1 Antibody, EAAT3 Antibody, Eaac-1 Antibody

SLC1A1 / EAAT3 is a member of the high-affinity glutamate transporters that play an essential role in transporting glutamate across plasma membranes. In brain, these transporters are crucial in terminating the postsynaptic action of the neurotransmitter glutamate, and in maintaining extracellular glutamate concentrations below neurotoxic levels.


IHC: Mouse anti-Glutamate Transporter [EAAC1] (LS-C152890) staining of rat cerebral cortex.
IHC: Mouse anti-Glutamate Transporter [EAAC1] (LS-C152890) staining of rat cerebral cortex.

Requested From: 
Date Requested: 4/26/2018

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