Glycine Amidinotransferase, Mitochondrial (GATM) Antibody

260€ (50 µg)
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935106861
info@markelab.com
name
Glycine Amidinotransferase, Mitochondrial (GATM) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx455478
tested applications
ELISA, WB, IHC
Description
Glycine Amidinotransferase, Mitochondrial (GATM) Antibody is a Rabbit polyclonal antibody for the detection of Human Glycine Amidinotransferase, Mitochondrial (GATM).
Documents del producto
Instrucciones
Data sheet
Product specifications
Category | Primary Antibodies |
Immunogen Target | Glycine Amidinotransferase, Mitochondrial (GATM) |
Host | Rabbit |
Reactivity | Human |
Recommended Dilution | Optimal dilutions/concentrations should be determined by the end user. |
Clonality | Polyclonal |
Conjugation | Unconjugated |
Isotype | IgG |
Size 1 | 50 µg |
Size 2 | 100 µg |
Form | Liquid |
Tested Applications | ELISA, WB, IHC |
Buffer | 0.01 M PBS, pH 7.4, 50% glycerol, 0.05% Proclin-300. |
Availability | Shipped within 5-12 working days. |
Storage | Store at 2-8 °C for up to 2 weeks. For long-term storage, aliquot and store at -80 °C. Avoid repeated freeze/thaw cycles. |
Dry Ice | No |
UniProt ID | P50440 |
Gene ID | 2628 |
NCBI Accession | NP_001473.1 |
Background | Antibody anti-GATM |
Status | RUO |
Descripción
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This gene encodes a mitochondrial enzyme that belongs to the amidinotransferase family. This enzyme is involved in creatine biosynthesis, whereby it catalyzes the transfer of a guanido group from L-arginine to glycine, resulting in guanidinoacetic acid, the immediate precursor of creatine. Mutations in this gene cause arginine:glycine amidinotransferase deficiency, an inborn error of creatine synthesis characterized by mental retardation, language impairment, and behavioral disorders.
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