GALK1 Antibody (PACO00835)
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주문- SKU:
- PACO00835
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Application:
- IHC
- Application:
- IF
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
Antibody Name: | GALK1 Antibody |
Antibody SKU: | PACO00835 |
Size: | 50ug |
Host Species: | Rabbit |
Tested Applications: | ELISA, WB, IHC, IF |
Recommended Dilutions: | WB:1:500-1:2000, IHC:1:100-1:300, IF:1:200-1:1000 |
Species Reactivity: | Human, Mouse, Rat |
Immunogen: | synthesized peptide derived from the N-terminal region of human GALK1. |
Form: | Liquid |
Storage Buffer: | Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide. |
Purification Method: | The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen. |
Clonality: | Polyclonal |
Isotype: | IgG |
Conjugate: | Non-conjugated |
Synonyms: | GALK1; GALK; Galactokinase; Galactose kinase |
UniProt Protein Function: | GALK1: Major enzyme for galactose metabolism. Defects in GALK1 are the cause of galactosemia II (GALCT2). Galactosemia 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. Belongs to the GHMP kinase family. GalK subfamily. |
UniProt Protein Details: | Protein type:Kinase, other; Carbohydrate Metabolism - galactose; EC 2.7.1.6; Carbohydrate Metabolism - amino sugar and nucleotide sugar Chromosomal Location of Human Ortholog: 17q24 Cellular Component: cytoplasm; cytosol; membrane Molecular Function:ATP binding; galactokinase activity; galactose binding Biological Process: galactose catabolic process; galactose metabolic process Disease: Galactokinase Deficiency |
NCBI Summary: | Galactokinase is a major enzyme for the metabolism of galactose and its deficiency causes congenital cataracts during infancy and presenile cataracts in the adult population. [provided by RefSeq, Jul 2008] |
UniProt Code: | P51570 |
NCBI GenInfo Identifier: | 1730187 |
NCBI Gene ID: | 2584 |
NCBI Accession: | P51570.1 |
UniProt Secondary Accession: | P51570,B2RC07, B4E1G6, |
UniProt Related Accession: | P51570 |
Molecular Weight: | 45,358 Da |
NCBI Full Name: | Galactokinase |
NCBI Synonym Full Names: | galactokinase 1 |
NCBI Official Symbol: | GALK1 |
NCBI Official Synonym Symbols: | GK1; GALK; HEL-S-19 |
NCBI Protein Information: | galactokinase |
UniProt Protein Name: | Galactokinase |
UniProt Synonym Protein Names: | Galactose kinase |
UniProt Gene Name: | GALK1 |
UniProt Entry Name: | GALK1_HUMAN |