ARG47091

anti-HOGA1 antibody

anti-HOGA1 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human

Overview

Product Description Mouse Monoclonal antibody recognizes HOGA1
Tested Reactivity Hu
Tested Application IHC-P, WB
Host Mouse
Clonality Monoclonal
Isotype IgG1
Target Name HOGA1
Antigen Species Human
Immunogen Recombinant protein of Human HOGA1.
Conjugation Un-conjugated
Alternate Names HOGA1; 4-hydroxy-2-oxoglutarate aldolase; mitochondrial; C10orf65; DHDPSL; Dihydrodipicolinate synthase-like; DHDPS-like protein; Probable 2-keto-4-hydroxyglutarate aldolase; Probable KHG-aldolase; Protein 569272

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P
WB
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purification with Protein A
Buffer PBS, 0.09% Sodium azide, 50% Glycerol and 0.5% BSA
Preservative 0.09% Sodium azide
Stabilizer 50% Glycerol and 0.5% BSA
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 112817 Human HOGA1

Swiss-port # Q86XE5 Human 4-hydroxy-2-oxoglutarate aldolase, mitochondrial

Gene Symbol HOGA1
Gene Full Name 4-hydroxy-2-oxoglutarate aldolase 1
Background The authors of PMID:20797690 cloned this gene while searching for genes in a region of chromosome 10 linked to primary hyperoxalurea type III. They noted that even though the encoded protein has been described as a mitochondrial dihydrodipicolinate synthase-like enzyme, it shares little homology with E. coli dihydrodipicolinate synthase (Dhdps), particularly in the putative substrate-binding region. Moreover, neither lysine biosynthesis nor sialic acid metabolism, for which Dhdps is responsible, occurs in vertebrate mitochondria. They propose that this gene encodes mitochondrial 4-hydroxyl-2-oxoglutarate aldolase (EC 4.1.3.16), which catalyzes the final step in the metabolic pathway of hydroxyproline, releasing glyoxylate and pyruvate. This gene is predominantly expressed in the liver and kidney, and mutations in this gene are found in patients with primary hyperoxalurea type III. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene. [provided by RefSeq, Nov 2010]
Function Catalyzes the final step in the metabolic pathway of hydroxyproline. [UniProt]
Calculated MW 35 kDa