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anti-Human MBOAT7 Antibodies:
anti-Mouse (Murine) MBOAT7 Antibodies:
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Human Polyclonal MBOAT7 Primary Antibody for WB - ABIN1881534
Gijón, Riekhof, Zarini, Murphy, Voelker: Lysophospholipid acyltransferases and arachidonate recycling in human neutrophils. in The Journal of biological chemistry 2008
Show all 2 Pubmed References
Dog (Canine) Polyclonal MBOAT7 Primary Antibody for WB - ABIN2783918
Blanchard, Taha, Cheon, Kim, Turk, Rapoport: iPLA2β knockout mouse, a genetic model for progressive human motor disorders, develops age-related neuropathology. in Neurochemical research 2014
Human Polyclonal MBOAT7 Primary Antibody for WB - ABIN4231381
Robichaud, Boulay, Munganyiki, Surette: Fatty acid remodeling in cellular glycerophospholipids following the activation of human T cells. in Journal of lipid research 2013
Children carrying the T allele of the MBOAT7 polymorphism had higher plasma alanine aminotransferase than the noncarriers; children with the MBOAT7, PNPLA3, and TM6SF2 variants had the highest plasma ALT
MBOAT7 polymorphism contributes to hepatic inflammation and liver fibrosis in patients with chronic hepatitis B.
Fibrosis stages were affected by the PNPLA3 (show PNPLA3 Antibodies) (P = 0.042) and MBOAT7 (P = 0.021) but not by the TM6SF2 polymorphism (P > 0.05). The PNPLA3 (show PNPLA3 Antibodies), TM6SF2, and MBOAT7 variants are associated with increased liver injury. The TM6SF2 variant seems to modulate predominantly hepatic fat accumulation, whereas the MBOAT7 polymorphism is linked to fibrosis. The PNPLA3 (show PNPLA3 Antibodies) polymorphism confers risk of both increased steatosis and fibrosis
identification of six consanguineous families harboring homozygous inactivating variants in MBOAT7, encoding lysophosphatidylinositol acyltransferase (LPIAT1); subjects presented with intellectual disability frequently accompanied by epilepsy and autistic features
Report an association between the MBOAT7 rs641738 variant and the development and severity of NAFLD (show TSC2 Antibodies) in individuals of European descent.
Variants in the MBOAT7 gene is associated with alcohol-related cirrhosis.
ssSPTa is identified as an LPIAT1-interacting protein.
MBOAT5 (show LPCAT3 Antibodies) and MBOAT7 in arachidonate recycling, thus regulating free arachidonic acid levels and leukotriene synthesis in neutrophils
LENG4 is located in the leukocyte receptor cluster on chromosome 19.
describes the cloning of human MBOAT7
These results suggest that LPEAT1/MBOAT1 (show MBOAT1 Antibodies) plays an important role in neurite outgrowth and function.
Data show that lysophosphatidylinositol acyltransferase 1 (LPIAT1, also known as MBOAT7) plays a crucial role in brain development in mice.
Congenital hydrocephalus (show FOXC1 Antibodies) in Mboat 7 null mice
Knockdown of class III PI 3 (show PI3 Antibodies)-kinase causes growth defects in mboa-7 mutants.
mboa-7 encodes a member of the membrane-bound O-acyltransferase family, suggesting that mboa-7 is lysoPI acyltransferase.
This gene encodes a member of the membrane-bound O-acyltransferases family of integral membrane proteins that have acyltransferase activity. The encoded protein is a lysophosphatidylinositol acyltransferase that has specificity for arachidonoyl-CoA as an acyl donor. This protein is involved in the reacylation of phospholipids as part of the phospholipid remodeling pathway known as the Land cycle. Alternative splicing results in multiple transcript variants.
, LPLAT 7
, bladder and breast carcinoma-overexpressed gene 1 protein
, leukocyte receptor cluster (LRC) member 4
, lyso-PI acyltransferase
, lysophosphatidylinositol acyltransferase
, lysophospholipid acyltransferase 7
, malignant cell expression-enhanced gene/tumor progression-enhanced
, O-acyltransferase domain-containing protein 7
, leukocyte receptor cluster member 4
, membrane-bound O-acyltransferase domain-containing protein 7