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Human PICALM ELISA Kit for Sandwich ELISA - ABIN417021
Agapova, Stephenson, Manary, Weisz, Tarr, Mkakosya, Maleta, Shulman, Manary, Shaikh: Detection of Low Concentration Host mRNA Transcripts in Malawian Children at Risk for Environmental Enteropathy. in Journal of pediatric gastroenterology and nutrition 2012
In this density functional theory study, reaction mechanisms of a co-catalytic binuclear metal center (Zn1-Zn2) containing enzyme leucine aminopeptidase (显示 LAP ELISA试剂盒) for two different metal bridging nucleophiles (H(2)O and -OH) have been investigated.
The LAP3 gene possibly contributed to conducting association analysis and can be used as molecular marker in milk production traits and other performance for animal breeding.
rs3851179 in PICALM was associated with an increased risk of gestational diabetes. The frequency of the Alzheimer's disease risk-associated C allele was significantly higher in the gestational diabetes group compared to controls. The C allele of the PICALM SNP was protective for impaired glucose tolerance.
Alzheimer's disease risk PICALM GG genotype suggests changes in the cortical excitatory-inhibitory balance, which are heightened during normal aging.
Study concludes that the novel clathrin interaction sites identified here in CALM and AP180 have a major role in how these proteins interface with clathrin. This work advances the case that AP180 and CALM are required to use a combination of standard clathrin N-terminal domain binding motifs and the sequence identified here for optimal binding and assembling clathrin.
Depletion of PICALM in brain-derived cells has significant effects on the processing of APP (显示 APP ELISA试剂盒), probably by reducing clathrin-mediated endocytosis. In particular, it affects the production of beta-C-terminal fragment which is increasingly considered to be an important mediator in Alzheimer's disease independent of Abeta (显示 APP ELISA试剂盒).
PICALM is involved with late onset Alzheimer's disease. [review]
Our finding suggests that PICALM rs3851179 could contribute to cognitive impairment in older patients with Parkinson disease
PICALM and CLU (显示 CLU ELISA试剂盒) risk genotypes exert differential impacts on the hippocampal resting-state functional connectivity in healthy young subjects.
PICALM has a role in modulating autophagy activity and tau accumulation
the rs541458 and rs3851179 of PICALM SNPs are not related to development of behavioral and psychological symptoms of dementia in Turkish population
We detected a significant association of the MTHFR (显示 MTHFR ELISA试剂盒) rs1801133 and PICALM rs3851179 polymorphisms with AD.
Confinement within the presynaptic bouton is mediated in part by synaptic vesicle protein association with the clathrin-based endocytic machinery to limit diffusional spread of newly exocytosed SV proteins.
the PICALM PIP2 binding domain is necessary for transferrin receptor endocytosis in erythroblasts and absolutely essential for erythroid development from mouse hematopoietic stem/progenitor cells in an erythroid culture system.
During leukemogenesis, CALM-AF10 (显示 MLLT10 ELISA试剂盒) plays critical roles in the cytoplasm.
These data reveal that PICALM plays a critical role in iron homeostasis.
PICALM, an adaptor protein involved in clathrin-mediated endocytosis, regulates APP (显示 APP ELISA试剂盒) internalization and subsequent Abeta (显示 APP ELISA试剂盒) generation. PICALM contributes to amyloid plaque load in brain likely via its effect on Abeta (显示 APP ELISA试剂盒) metabolism.
These results indicate that CALM is required for erythroid maturation and transferrin (显示 Tf ELISA试剂盒) internalization in mice.
In leukemia cells, full-length CALM-AF10 localized to the nucleus with no consistent effect on growth factor endocyctosis, and suppressed histone H3 lysine 79 methylation regardless of the presence of clathrin
the Rarb (显示 RARB ELISA试剂盒) region of Mmu14 and Stmn2 (显示 STMN2 ELISA试剂盒), but not Cr1 (显示 TDGF1 ELISA试剂盒) or Clu (显示 CLU ELISA试剂盒) or Picalm have roles in prion (显示 PRNP ELISA试剂盒) disease
fit14R & fit15R are nonsense point mutations in the mouse PICALM gene. They are splice-donor alterations causing transcripts less abundant transcripts missing exons 4 & 17, respectively. The protein is truncated near the N or C termini, respectively.
results reveal a new mode by which AP180 couples protein retrieval to CME of SVs (显示 FGFR2 ELISA试剂盒)
clathrin adapter protein (显示 GRB10 ELISA试剂盒)
This gene encodes a clathrin assembly protein, which recruits clathrin and adaptor protein complex 2 (AP2) to cell membranes at sites of coated-pit formation and clathrin-vesicle assembly. The protein may be required to determine the amount of membrane to be recycled, possibly by regulating the size of the clathrin cage. The protein is involved in AP2-dependent clathrin-mediated endocytosis at the neuromuscular junction. A chromosomal translocation t(10\;11)(p13\;q14) leading to the fusion of this gene and the MLLT10 gene is found in acute lymphoblastic leukemia, acute myeloid leukemia and malignant lymphomas. The polymorphisms of this gene are associated with the risk of Alzheimer disease. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene.
, cytosol aminopeptidase
, leucyl aminopeptidase
, proline aminopeptidase
, prolyl aminopeptidase
, peptidase S
, clathrin assembly lymphoid myeloid leukemia protein
, phosphatidylinositol-binding clathrin assembly protein
, clathrin assembly lymphoid myeloid leukemia
, clathrin-assembly lymphoid leukemia protein
, clathrin-assembly lymphoid myeloid leukemia protein
, complementation group 12
, like AP180
, uncharacterized protein LOC772071