Use your antibodies-online credentials, if available.
No Products on your Comparison List.
Your basket is empty.
Find out more
The protein encoded by LSAMP is a neuronal surface glycoprotein found in cortical and subcortical regions of the limbic system. Additionally we are shipping Limbic System-Associated Membrane Protein Proteins (10) and Limbic System-Associated Membrane Protein Kits (3) and many more products for this protein.
Showing 10 out of 34 products:
We detected African-specific SNPs at ZNF649 (show ZNF649 Antibodies) and LSAMP, with associations of genome-wide significance for ulcerative colitis.
A novel genomic alteration of LSAMP associates with aggressive prostate cancer in African American men
The results showed significant allelic and haplotypic associations between LSAMP gene and schizophrenia.
The tumor suppressor function of LSAMP is most likely exerted by reducing the proliferation rate of the tumor cells, possibly by indirectly upregulating one or more of the genes HES1, CTAG2 (show CTAG2 Antibodies) or KLF10 (show KLF10 Antibodies).
This study presents the first evidence of a possible role of LSAMP gene in mood and anxiety disorders in humans.
proteomic assessments of membrane microdomains in prefrontal cortex and validation in two brain series, strongly implicates LAMP, STXBP1 (show STXBP1 Antibodies) and BASP1 (show BASP1 Antibodies) in schizophreina and supports the view of a neuritic and synaptic dysfunction in the neuropathology
Single nucleotide polymorphisms of LSAMP is associated with the pathogenesis of coronary artery disease.
LSAMP might play a role in pathoaetiology of suicidal behaviour but further studies are needed to understand its exact contribution
results show that LSAMP is a novel candidate tumor suppressor gene in osteosarcomas
Identification of chromosomal aberrations associated with disease progression and a novel 3q13.31 deletion involving LSAMP gene in osteosarcoma.
Limbic system-associated membrane protein is involved in emotional and social operating systems by complex regulation of two alternative promoters.
Lsamp(-/-) mice are a promising model to study the neurobiological mechanisms of deviant social behaviour and adaptation impairment observed in many psychiatric disorders.
Lsamp-deficient mice were less sensitive to isolation stress than their wild-type littermates.
lsamp knockout mice have a deficit in spatial memory acquisition and poorly sustained CA1 (show CA1 Antibodies) long-term potentiation.
genomic features of the Lsamp gene indicate an intricate mechanism of gene expression regulation that may be relevant in the context of human neuropsychiatric and neurological disorders, where LAMP expression may be altered
Genetic deletion of Lsamp causes exaggerated behavioral activation in novel environments.
The protein encoded by this gene is a neuronal surface glycoprotein found in cortical and subcortical regions of the limbic system. During development of the limbic system, this encoded protein is found on the surface of axonal membranes and growth cones, where it acts as a selective homophilic adhesion molecule, and guides the development of specific patterns of neuronal connections.
, E19S protein
, IgLON family member 3
, limbic system-associated membrane protein