Description
Antibody Name: | PHYKPL Antibody (PACO15355) |
Antibody SKU: | PACO15355 |
Size: | 50ul |
Host Species: | Rabbit |
Tested Applications: | ELISA, WB |
Recommended Dilutions: | ELISA:1:2000-1:5000, WB:1:500-1:2000 |
Species Reactivity: | Human, Mouse |
Immunogen: | Fusion protein of human AGXT2L2 |
Form: | Liquid |
Storage Buffer: | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
Purification Method: | Antigen affinity purification |
Clonality: | Polyclonal |
Isotype: | IgG |
Conjugate: | Non-conjugated |
![]() | Gel: 8%SDS-PAGE, Lysate: 40 μg, Lane: Human lymphoma tissue, Primary antibody: PACO15355(AGXT2L2 Antibody) at dilution 1/500, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 30 seconds. |
Background: | 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. |
Synonyms: | 5-phosphohydroxy-L-lysine phospho-lyase |
UniProt Protein Function: | AGXT2L2: Catalyzes the pyridoxal-phosphate-dependent breakdown of 5-phosphohydroxy-L-lysine, converting it to ammonia, inorganic phosphate and 2-aminoadipate semialdehyde. Belongs to the class-III pyridoxal-phosphate-dependent aminotransferase family. 3 isoforms of the human protein are produced by alternative splicing.Protein type: EC 4.2.3.134; TransferaseChromosomal Location of Human Ortholog: 5q35.3Cellular Component: mitochondrial matrixMolecular Function: identical protein binding; lyase activity; protein binding; pyridoxal phosphate binding; transaminase activityBiological Process: collagen catabolic process; extracellular matrix disassembly; extracellular matrix organization and biogenesis; lysine catabolic processDisease: Phosphohydroxylysinuria |
UniProt Protein Details: | |
NCBI Summary: | 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 Code: | Q8IUZ5 |
NCBI GenInfo Identifier: | 74750645 |
NCBI Gene ID: | 85007 |
NCBI Accession: | Q8IUZ5.1 |
UniProt Secondary Accession: | Q8IUZ5,Q8WYS6, Q96HW8, A8K7P6, B3KN36, D3DWP9 |
UniProt Related Accession: | Q8IUZ5 |
Molecular Weight: | 18,857 Da |
NCBI Full Name: | 5-phosphohydroxy-L-lysine phospho-lyase |
NCBI Synonym Full Names: | 5-phosphohydroxy-L-lysine phospho-lyase |
NCBI Official Symbol: | PHYKPL |
NCBI Official Synonym Symbols: | PHLU; AGXT2L2 |
NCBI Protein Information: | 5-phosphohydroxy-L-lysine phospho-lyase |
UniProt Protein Name: | 5-phosphohydroxy-L-lysine phospho-lyase |
UniProt Synonym Protein Names: | Alanine--glyoxylate aminotransferase 2-like 2 |
Protein Family: | |
UniProt Gene Name: | PHYKPL |
UniProt Entry Name: | AT2L2_HUMAN |