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The protein encoded by PLEKHM1 is essential for bone resorption, and may play a critical role in vesicular transport in the osteoclast. Additionally we are shipping PLEKHM1 Proteins (4) and many more products for this protein.
Showing 10 out of 44 products:
Human Polyclonal PLEKHM1 Primary Antibody for EIA, WB - ABIN954203
Edwards, Scott, Almonte, Burt, Powell, Beecham, Wang, Züchner, Konidari, Wang, Singer, Nahab, Scott, Stajich, Pericak-Vance, Haines, Vance, Martin: Genome-wide association study confirms SNPs in SNCA and the MAPT region as common risk factors for Parkinson disease. in Annals of human genetics 2010
Show all 3 references for ABIN954203
Human Polyclonal PLEKHM1 Primary Antibody for EIA, IHC (p) - ABIN500509
van Wesenbeeck, Odgren, Mackay, Van Hul: Localization of the gene causing the osteopetrotic phenotype in the incisors absent (ia) rat on chromosome 10q32.1. in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2004
Show all 3 references for ABIN500509
identified PLEKHM1 as an endolysosomal adaptor platform that acts as a central hub to integrate endocytic and autophagic pathways at the lysosome
Authors show that Pleckstrin (show PLEK Antibodies) homology domain-containing protein family member 1 (PLEKHM1), a lysosomal adaptor, is targeted by Salmonella through direct interaction with SifA.
PLEKHM1 regulates autophagosome-lysosome fusion through homotypic fusion and protein sorting complex and LC3 (show MAP1LC3A Antibodies)/GABARAP (show GABARAP Antibodies) proteins.
Rubicon (show KIAA0226 Antibodies) and PLEKHM1 specifically and directly interact with Rab7 (show RAB7B Antibodies) via their RH domain; this interaction is critical for their function; show Rubicon (show KIAA0226 Antibodies) but not PLEKHM1 uniquely regulates membrane trafficking via simultaneously binding both Rab7 (show RAB7B Antibodies) and PI3-kinase (show PIK3CA Antibodies)
These data indicate that B2 is a novel, ubiquitously expressed protein with a putative adapter function. The protein has been named AP162.
PLEKHM1 is a novel gene implicated in the development of osteopetrosis (show CSF1 Antibodies), with a putative critical function in vesicular transport in the osteoclast.
heterozygous mutation (R714C) of the osteopetrosis (show CSF1 Antibodies) gene, pleckstrin (show PLEK Antibodies) homolog domain containing family M (with run domain) member 1 (PLEKHM1), impairs vesicular acidification and increases TRACP (show ACP5 Antibodies) secretion in osteoclasts
TRAFD1 (show TRAFD1 Antibodies), in association with Plekhm1/Rab7 (show RAB7A Antibodies)-positive late endosomes-early lysosomes, has a previously unknown role in vesicle trafficking, acidification, and resorption in osteoclasts
results indicate that LIS1 (show PAFAH1B1 Antibodies) is a previously unrecognized regulator of osteoclast formation, microtubule organization, and lysosomal secretion by virtue of its ability to modulate dynein function and Plekhm1
The protein encoded by this gene is essential for bone resorption, and may play a critical role in vesicular transport in the osteoclast. Mutations in this gene are associated with autosomal recessive osteopetrosis type 6 (OPTB6). Alternatively spliced transcript variants have been found for this gene.
pleckstrin homology domain containing, family M (with RUN domain) member 1
, 162 kDa adapter protein
, PH domain-containing family M member 1
, pleckstrin homology domain-containing family M member 1