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Mouse Anti-AGXT Recombinant Antibody (1F9BC7) (CBMAB-A1687-YC)

Provided herein is a Mouse monoclonal antibody against Human Alanine-Glyoxylate Aminotransferase. The antibody can be used for immunoassay techniques, such as ELISA, ICC, IP.
See all AGXT antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
V2-180254
Antibody Isotype
IgG1, κ
Application
WB

Basic Information

Immunogen
AGXT Fusion Protein Ag19188.
Host Species
Mouse
Specificity
Human
Antibody Isotype
IgG1, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.
ApplicationNote
WB1:5,000

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
HEPES, 0.02% sodium azide
Buffer
PBS, pH7.3, 50% glycerol
Preservative
0.02% sodium azide
Concentration
1 mg/ml
Storage
Store at 4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Alanine-Glyoxylate Aminotransferase
Introduction
AGXT is expressed only in the liver and the encoded protein is localized mostly in the peroxisomes, where it is involved in glyoxylate detoxification. Mutations in this gene, some of which alter subcellular targetting, have been associated with type I pri
Entrez Gene ID
Human189
Mouse11611
Rat24792
UniProt ID
HumanP21549
MouseO35423
RatP09139
Alternative Names
Alanine-Glyoxylate Aminotransferase; L-Alanine: Glyoxylate Aminotransferase 1; SPAT; AGT1; AGT; SPT; Hepatic Peroxisomal Alanine:Glyoxylate Aminotransferase; Alanine--Glyoxylate Aminotransferase; Serine--Pyruvate Aminotransferase; Serine:Pyruvate Aminotra
Biological Process
Carboxylic acid metabolic process
Glycine biosynthetic process, by transamination of glyoxylate
Glyoxylate catabolic process
Glyoxylate metabolic process
L-alanine catabolic process
L-cysteine catabolic process
Protein localization
Pyruvate biosynthetic process
Response to cAMP
Response to glucocorticoid
Cellular Location
Peroxisome; Mitochondrion. Predominantly localized in the peroxisomes. Mitochondrial mistargeting occurs in variant proteins Arg-41, Arg-47, Ile-152, Arg-170 and Thr-244 associated with the disease HP1.
Involvement in disease
Hyperoxaluria primary 1 (HP1): An inborn error of glyoxylate metabolism characterized by increased excretion of oxalate and glycolate, and progressive tissue accumulation of insoluble calcium oxalate. Affected individuals are at risk for nephrolithiasis, nephrocalcinosis and early onset end-stage renal disease.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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