GALK1 Protein (GST tag,His tag)
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- Target See all GALK1 Proteins
- GALK1 (Galactokinase 1 (GALK1))
- Protein Type
- Recombinant
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Origin
- Human
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Source
- Baculovirus infected Insect Cells
- Purification tag / Conjugate
- This GALK1 protein is labelled with GST tag,His tag.
- Purpose
- Recombinant Human GALK1/Galactokinase Protein (His & GST Tag)
- Sequence
- Met 1-Leu 392
- Characteristics
- A DNA sequence encoding the human GALK1 (P51570) (Met 1-Leu 392) was fused with the N-terminal polyhistidine-tagged GST tag at the N-terminus.
- Purity
- > 90 % as determined by reducing SDS-PAGE.
- Endotoxin Level
- < 1.0 EU per μg as determined by the LAL method.
- Top Product
- Discover our top product GALK1 Protein
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- Restrictions
- For Research Use only
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- Format
- Frozen, Liquid
- Buffer
- Supplied as sterile 20 mM Tris, 500 mM NaCl, 2 mM GSH, pH 8.0
- Storage
- -20 °C
- Storage Comment
- Store at < -20°C, stable for 6 months. Please minimize freeze-thaw cycles.
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- Target
- GALK1 (Galactokinase 1 (GALK1))
- Alternative Name
- GALK1/Galactokinase (GALK1 Products)
- Synonyms
- GALK Protein, GK1 Protein, AA409894 Protein, Gk Protein, Glk Protein, Glk1 Protein, Galk Protein, galactokinase 1 Protein, GALK1 Protein, Galk1 Protein
- Background
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Background: Galactokinase; also known as Galactose kinase; GALK and GALK1; is a protein which belongs to the GHMP kinase family and GalK subfamily. Galactokinase / GALK1 is a major enzyme for galactose metabolism. Galactokinase (GALK) deficiency is an autosomal recessive disorder characterized by elevation of blood galactose concentration and diminished galactose-1-phosphate; leading to the production of galactitol. Defects in GALK1 are the cause of galactosemia II ( GALCT2 ) which II is an autosomal recessive deficiency characterized by congenital cataracts during infancy and presenile cataracts in the adult population. The cataracts are secondary to accumulation of galactitol in the lenses.
Synonym: Galactokinase; Galactose Kinase; GALK1; GALK
- Molecular Weight
- 70 kDa
- UniProt
- P51570
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