Galactose-1-Phosphate Uridylyltransferase (GALT) Antibody

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312€ (60 µl)

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935106861
info@markelab.com
name
Galactose-1-Phosphate Uridylyltransferase (GALT) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx004808
tested applications
WB

Description

GALT Antibody is a Rabbit Polyclonal antibody against GALT. Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Galactose-1-Phosphate Uridylyltransferase (GALT)
Host
Rabbit
Reactivity
Human
Recommended Dilution
WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
60 µl
Size 2
120 µl
Size 3
200 µl
Form
Liquid
Tested Applications
WB
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P07902
Gene ID
2592
NCBI Accession
NP_000146.2
Background
Antibody anti-GALT
Status
RUO
Note
Concentration: 1 mg/ml -

Descripción

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Galactose-1-Phosphate Uridylyltransferase (GALT) Antibody

GALT Antibody is a Rabbit Polyclonal antibody against GALT. Galactose-1-phosphate uridyl transferase (GALT) catalyzes the second step of the Leloir pathway of galactose metabolism, namely the conversion of UDP-glucose + galactose-1-phosphate to glucose-1-phosphate + UDP-galactose. The absence of this enzyme results in classic galactosemia in humans and can be fatal in the newborn period if lactose is not removed from the diet. The pathophysiology of galactosemia has not been clearly defined. Two transcript variants encoding different isoforms have been found for this gene.

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