KO Validated Antibodies 2
Anti-HAGH Antibody (CAB19915)[KO Validated]
- SKU:
- CAB19915
- Product Type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Cell Biology
Description
Antibody Name: | Anti-HAGH Antibody [KO Validated] |
Antibody SKU: | CAB19915 |
Antibody Size: | 20uL, 50uL, 100uL |
Application: | WB IHC IF |
Reactivity: | Human, Mouse, Rat |
Host Species: | Rabbit |
Immunogen: | Recombinant protein of human HAGH. |
Application: | WB IHC IF |
Recommended Dilution: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 IF 1:10 - 1:100 |
Reactivity: | Human, Mouse, Rat |
Positive Samples: | HeLa |
Immunogen: | Recombinant protein of human HAGH. |
Purification Method: | Affinity purification |
Storage Buffer: | Store at -20°C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
Isotype: | IgG |
Sequence: | Email for sequence |
Gene ID: | 3029 |
Uniprot: | Q16775 |
Cellular Location: | Cytoplasm, Mitochondrion matrix |
Calculated MW: | 25kDa/28kDa/33kDa |
Observed MW: | 30KDa |
Synonyms: | HAGH, GLO2, GLX2, GLXII, HAGH1 |
Background: | The enzyme encoded by this gene is classified as a thiolesterase and is responsible for the hydrolysis of S-lactoyl-glutathione to reduced glutathione and D-lactate. Three transcript variants encoding different isoforms have been found for this gene. |
UniProt Protein Function: | HAGH: Thiolesterase that catalyzes the hydrolysis of S-D- lactoyl-glutathione to form glutathione and D-lactic acid. Belongs to the metallo-beta-lactamase superfamily. Glyoxalase II family. 2 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Mitochondrial; EC 3.1.2.6; Carbohydrate Metabolism - pyruvate; Hydrolase Chromosomal Location of Human Ortholog: 16p13.3 Cellular Component: mitochondrial matrix; cytoplasm Molecular Function:hydroxyacylglutathione hydrolase activity; zinc ion binding Biological Process: glutathione biosynthetic process Disease: Hydroxyacyl Glutathione Hydrolase Deficiency |
NCBI Summary: | The enzyme encoded by this gene is classified as a thiolesterase and is responsible for the hydrolysis of S-lactoyl-glutathione to reduced glutathione and D-lactate. Three transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2013] |
UniProt Code: | Q16775 |
NCBI GenInfo Identifier: | 257051015 |
NCBI Gene ID: | 3029 |
NCBI Accession: | Q16775.2 |
UniProt Secondary Accession: | Q16775,A8K290, B4DP33, B4DRA7, E7EN93, |
UniProt Related Accession: | Q16775 |
Molecular Weight: | 308 |
NCBI Full Name: | Hydroxyacylglutathione hydrolase, mitochondrial |
NCBI Synonym Full Names: | hydroxyacylglutathione hydrolase |
NCBI Official Symbol: | HAGH |
NCBI Official Synonym Symbols: | GLO2; GLX2; GLXII; HAGH1 |
NCBI Protein Information: | hydroxyacylglutathione hydrolase, mitochondrial; glx II; glyoxalase II; hydroxyacylglutathione hydroxylase |
UniProt Protein Name: | Hydroxyacylglutathione hydrolase, mitochondrial |
UniProt Synonym Protein Names: | Glyoxalase II; Glx II |
UniProt Gene Name: | HAGH |
UniProt Entry Name: | GLO2_HUMAN |