Serine/Threonine-Protein Kinase PINK1, Mitochondrial (PINK1) Antibody
292.5€ (50 µl)
Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.
935106861
info@markelab.com
name
Serine/Threonine-Protein Kinase PINK1, Mitochondrial (PINK1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx025541
tested applications
ELISA, WB, IHC, IF/ICC
Description
This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease.
Documents del producto
Instrucciones
Data sheet
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | Serine/Threonine-Protein Kinase PINK1, Mitochondrial (PINK1) |
| Host | Mouse |
| Reactivity | Human |
| Recommended Dilution | WB: 1/1000, IHC-P: 1/25, IF/ICC: 1/25. Not tested in IHC-F. Optimal dilutions/concentrations should be determined by the end user. |
| Clonality | Monoclonal |
| Conjugation | Unconjugated |
| Isotype | IgG1 |
| Purification | Purified through a protein G column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS. |
| Size 1 | 50 µl |
| Size 2 | 200 µl |
| Form | Liquid |
| Tested Applications | ELISA, WB, IHC, IF/ICC |
| 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 | Q9BXM7 |
| NCBI Accession | NP_115785.1 |
| Background | Antibody anti-PINK1 |
| Status | RUO |
Descripción
Related Products
Human PINK1 (Serine/threonine-protein kinase PINK1, mitochondrial) ELISA Kit
Ver Producto
Mouse PINK1(Serine/threonine-protein kinase PINK1, mitochondrial) ELISA Kit
Ver Producto
PINK1 antibody
This gene encodes a serine/threonine protein kinase that localizes to mitochondria. It is thought to protect cells from stress-induced mitochondrial dysfunction. Mutations in this gene cause one form of autosomal recessive early-onset Parkinson disease.
Ver Producto