Alanine Glyoxylate Aminotransferase (AGXT) Antibody Pair

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1170€ (5 × 96 tests)

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935106861
info@markelab.com
name
Alanine Glyoxylate Aminotransferase (AGXT) Antibody Pair
category
Antibody Pairs
provider
Abbexa
reference
abx370894
tested applications
ELISA

Description

Alanine Glyoxylate Aminotransferase (AGXT) Antibody Pair for use in Sandwich ELISA assay development.
This antibody pair contains:
Detection: 50 µg
Capture: 200 µg
Standard: 5 µg

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Antibody Pairs
Immunogen Target
Alanine Glyoxylate Aminotransferase (AGXT)
Host
Capture Host: Rabbit
Detection Host: Rabbit
Reactivity
Human
Assay Data
Sandwich
Assay Type
Capture Antibody: 0.5 mg/ml  Biotin-Conjugated Detection Antibody: 0.2 mg/ml
Reconstitute the standard with Standard Diluent. The volume, and therefore standard concentration, should be determined by the end user. For a standard curve range of 1.56 ng/ml - 100 ng/ml, a reconstitution volume of 1 ml is recommended.
Test Range
1.56 ng/ml - 100 ng/ml
Recommended Dilution
Dilute the Capture Antibody 125-fold with Coating Buffer.  Dilute the Biotin-Conjugated Detection Antibody 200-fold with Detection Antibody Diluent.  Optimal dilutions/concentrations should be determined by the end user.
Clonality
Capture Clonality: Polyclonal
Detection Clonality: Polyclonal
Conjugation
Biotin
Size 1
5 × 96 tests
Size 2
10 × 96 tests
Form
Standard form: Lyophilized
Capture Ab: Liquid
Detection Ab: Liquid
Tested Applications
ELISA
Buffer
The Capture and Detection Antibody both contain 0.1% sodium azide.
Availability
Shipped within 5-20 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
Alias
AGXT, AGT1, SPAT
Background
Antibody pair for AGXT
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Descripción

Alanine-glyoxylate aminotransferase (AGXT) is a pyridoxal phosphate-dependent enzyme localized in peroxisomes, where it plays a critical role in detoxifying glyoxylate by converting it into glycine, using alanine as an amino donor. AGXT is central to preventing the overproduction of oxalate, a byproduct of glyoxylate metabolism, which, if accumulated, can form calcium oxalate crystals leading to kidney stones and renal damage. Mutations in the AGXT gene cause primary hyperoxaluria type 1 (PH1), a rare autosomal recessive disorder characterized by excessive oxalate production, kidney stone formation, and systemic oxalosis. AGXT's activity is regulated by intracellular localization and metabolic cues, and therapies targeting AGXT include enzyme replacement therapy and gene therapy to restore glyoxylate metabolism in affected individuals.

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