Specifications
- Antibody type:Primary
- Antigen name:GALE/Galactowaldenase
- Clonality:Polyclonal
- Conjugation:Alexa Fluor® 680
- Host:Rabbit
- ImmunoChemistry:Yes
- ImmunoFluorescence:Yes
- Isotype:IgG
- Reactivity:Mouse
- Western blot:Yes
- Environmentally Preferable:
- Epitope:21-120/348
- Form:Liquid
- Gene ID:2582
- Antigen synonyms:UDP-glucose 4-epimerase|GALE_HUMAN|SDR1E1|FLJ95174|OTTHUMP00000044857|Galactowaldenase|Galactose 4 epimerase UDP|short chain dehydrogenase/reductase family 1E member 1|galE|OTTHUMP00000037931|UDP glucose 4 epimerase|UDP-galactose 4-epimerase|UDP galactose 4 epimerase|OTTHUMP00000002994|FLJ97302|OTTHUMP00000002991
- Modification:Unmodified
- Storage buffer:Aqueous buffered solution containing 0,01M TBS (pH 7,4) with 1% BSA, 0,03% Proclin300 and 50% Glycerol.
- Molecular weight:38 kDa
- Storage temperature:Store at −20 °C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Concentration:1 µg/µl
- Shipping temperature:4 °C
- Immunogen:KLH conjugated synthetic peptide derived from human GALE/Galactowaldenase
- Tested applications:ICC
- Purification:Purified by Protein A
- Pack type:Vial
- Pk:100 µl
Specifications
About this item
GALE is a 348 amino acid protein that functions as the third enzyme in the Leloir pathway of galactose metabolism. A member of the sugar epimerase family, GALE exists as a homodimer, binds FAD as a cofactor and catalyzes the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine and UDP-glucose to UDP-galactose. The gene encoding GALE maps to human chromosome 1p36.11 and mutations in this gene lead to the development of complex disorder known as epimerase-deficiency galactosemia (EDG) or galactosemia type 3, which is characterized by mental retardation, liver damage, cataracts and deafness.
Type: Primary
Antigen: GALE/Galactowaldenase
Clonality: Polyclonal
Clone:
Conjugation: ALEXA FLUOR® 680
Public Immunogen Range: 21-120/348
Host: Rabbit
Isotype: IgG
Reactivity: Mouse