GTP Binding Protein 3 (Mitochondrial) (GTPBP3) Antibody

292.5€ (80 µl)
Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
935106861
info@markelab.com
name
GTP Binding Protein 3 (Mitochondrial) (GTPBP3) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx031073
tested applications
ELISA, WB
Description
This locus encodes a GTP-binding protein. The encoded protein is localized to the mitochondria and may play a role in mitochondrial tRNA modification. Polymorphisms at this locus may be associated with severity of aminoglycoside-induced deafness, a disease associated with a mutation in the 12S rRNA. Alternatively spliced transcript variants encoding different isoforms have been described.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | GTP Binding Protein 3 (Mitochondrial) (GTPBP3) |
| Host | Rabbit |
| Reactivity | Human |
| Recommended Dilution | WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Purification | Purified through a protein A column, followed by peptide affinity purification. |
| Size 1 | 80 µl |
| Size 2 | 400 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB |
| Buffer | PBS containing 0.09% sodium azide. |
| Availability | Shipped within 5-10 working days. |
| Storage | Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles. |
| Dry Ice | No |
| UniProt ID | Q969Y2 |
| Background | Antibody anti-GTPBP3 |
| Status | RUO |
Descripción
Related Products

GTPBP3 antibody
GTPase involved in the 5-carboxymethylaminomethyl modification(mnm(5)s(2)U34) of the wobble uridine base in mitochondrial tRNAs.
Ver Producto
Recombinant Human GTPBP3
Ver Producto
GTP Binding Protein 3 (Mitochondrial) (GTPBP3) Antibody
This locus encodes a GTP-binding protein. The encoded protein is localized to the mitochondria and may play a role in mitochondrial tRNA modification. Polymorphisms at this locus may be associated with severity of aminoglycoside-induced deafness, a disease associated with a mutation in the 12S rRNA. Alternatively spliced transcript variants encoding different isoforms have been described.
Ver Producto