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Anti-HCAR2 / NIACR1 Antibody (aa200-228) LS-C164871


Wt. Vol. Conc. Price
- 400 µl - Unavailable

Related Products

14 HCAR2 / NIACR1 Antibodies

Most Popular HCAR2 / NIACR1 Antibodies

Anti-HCAR2 / NIACR1 Antibody (aa200-228) LS-C164871
Rabbit Polyclonal to Human HCAR2 / NIACR1
Western blot
Western blot Image
Anti-HCAR2 / NIACR1 Antibody (aa207-236, AP) LS-C238028
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Anti-HCAR2 / NIACR1 Antibody (aa207-236, APC) LS-C238029
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Anti-HCAR2 / NIACR1 Antibody LS-C403190
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Anti-HCAR2 / NIACR1 Antibody LS-C406433
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Rabbit Polyclonal to Human HCAR2 / NIACR1
Western blot


Human HCAR2 / NIACR1
Human (tested or 100% immunogen sequence identity)
Mouse (at least 90% immunogen sequence identity)
Protein A purified


Western blot (1:1000)

Specificity and Use

LS-E1854 - Lyophilized - 100 µg - $145.00
Immunizing peptide used to generate LS-C164871. Useful for pre-absorption and neutralization of the antibody's antigen binding site.
This NIACR1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 200-228 amino acids from the Central region of human NIACR1.


PBS, 0.09% sodium azide
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C.
For research use only.

About HCAR2 / NIACR1

Q8TDS4 AB083632 BAB89345.1

HCAR2 Antibody, GPR109A Antibody, HCA2 Antibody, NIACR1 Antibody, Nicotinic acid receptor Antibody, HM74a Antibody, HM74b Antibody, Niacin receptor 1 Antibody, Puma-g Antibody, PUMAG Antibody

Acts as a high affinity receptor for both nicotinic acid (also known as niacin) and (D)-beta-hydroxybutyrate and mediates increased adiponectin secretion and decreased lipolysis through G(i)-protein-mediated inhibition of adenylyl cyclase. This pharmacological effect requires nicotinic acid doses that are much higher than those provided by a normal diet. Mediates nicotinic acid-induced apoptosis in mature neutrophils.

Western blot

Western blot
NIACR1 Antibody western blot of NCI-H292 cell line lysates (35 ug/lane). The NIACR1 antibody detected the NIACR1 protein (arrow).

Requested From: 
Date Requested: 4/23/2017

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