AGXT2L2 rabbit pAb
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AGXT2L2 rabbit pAb
Background :
5-phosphohydroxy-L-lysine phospho-lyase (PHYKPL) Homo sapiens This is a nuclear gene encoding a mitochondrial enzyme that catalyzes the conversion of 5-phosphonooxy-L-lysine to ammonia, inorganic phosphate, and 2-aminoadipate semialdehyde. Mutations in this gene may cause phosphohydroxylysinuria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013]Description :
5-phosphohydroxy-L-lysine phospho-lyase (PHYKPL) Homo sapiens This is a nuclear gene encoding a mitochondrial enzyme that catalyzes the conversion of 5-phosphonooxy-L-lysine to ammonia, inorganic phosphate, and 2-aminoadipate semialdehyde. Mutations in this gene may cause phosphohydroxylysinuria. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2013],UniProt :
Q8IUZ5Swiss Prot :
Q8IUZ5Reactivity :
Human; Mouse; RatImmunogen :
The antiserum was produced against synthesized peptide derived from human AGXT2L2. AA range:341-390Clonality :
PolyclonalSource :
RabbitApplications :
WB; IHC; IF; ELISAConcentration :
1 mg/mlDilution :
Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/10000. Not yet tested in other applications.Molecular Weight :
50kDStorage Conditions :
-20°C/1 yearObserved Molecular Weight :
50kDFragment :
IgGSubcellular Location :
Mitochondrion .Other Product Names :
AGXT2L2; PP9286; 5-phosphohydroxy-L-lysine phospho-lyase; Alanine--glyoxylate aminotransferase 2-like 2Gene ID (Human) :
85007

