PAFAH1B1, Rabbit, Polyclonal Antibody, Abnova
Rabbit polyclonal antibody raised against synthetic peptide of PAFAH1B1.
Manufacturer: Abnova Corporation PAB13006
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 noncatalytic 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
|Western Blot (0.5-1 ug/mL) The optimal working dilution should be determined by the end user.|
|Store at 4°C for three months. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.
|Human, Murine, Rat|
|Rabbit polyclonal antibody raised against synthetic peptide of PAFAH1B1.|
|In PBS (0.02% sodium azide)|
|A synthetic peptide corresponding to C-terminus 14 amino acids of human PAFAH1B1.|
For Research Use Only