Tissue expression
Cell line expression
Protein structure
PAFAH1B1
Platelet activating factor acetylhydrolase 1b regulatory subunit 1LIS1, MDCR, MDS, NudF, PAFAH
This locus was identified as encoding a gene that when mutated or lost caused the lissencephaly associated with Miller-Dieker lissencephaly syndrome. This gene encodes the non-catalytic alpha subunit of the intracellular Ib isoform of platelet-activating factor acteylhydrolase, a heterotrimeric enzyme that specifically catalyzes the removal of the acetyl group at the SN-2 position of platelet-activating factor (identified as 1-O-alkyl-2-acetyl-sn-glyceryl-3-phosphorylcholine). Two other isoforms of intracellular platelet-activating factor acetylhydrolase exist: one composed of multiple subunits, the other, a single subunit. In addition, a single-subunit isoform of this enzyme is found in serum. [provided by RefSeq, Apr 2009]
Top validated antibodies |
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Novus Biologicals | NBP1-03125 | 2 references | Polyclonal |
WB
EL
ICC
IHC |
|
antibodies-online | ABIN2493017 | Polyclonal |
WB
ICC
IHC
FC |
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Invitrogen Antibodies | PA5-20419 | 1 references | Polyclonal |
WB
ICC
OA
|
|
Abnova Corporation | H00005048-M03 | Monoclonal |
WB
EL
ICC
|
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Atlas Antibodies | HPA020036 | Polyclonal |
WB
ICC
IHC
|
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Supportive data in Antibodypedia
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Recommended by provider