Serine/Threonine-Protein Kinase PINK1, Mitochondrial (PINK1) Antibody (FITC)

Product Graph
637€ (100 µg)

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 (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx443299
tested applications
WB, IHC, IF/ICC

Description

PINK1 Antibody is a Mouse Monoclonal against PINK1.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Target: Serine/Threonine-Protein Kinase PINK1, Mitochondrial (PINK1)
Immunogen: Fusion protein amino acids 112-496 (cytoplasmic C-terminus) of human PINK1. 82% identical to rat and 81% identical to mouse. >30% identity with DMPK..
Host
Mouse
Reactivity
Human, Mouse, Rat
Detection Method
Laser Line: 488
Excitation/Emission: 499/515
Assay Type
Concentration: 1 mg/ml
Recommended Dilution
WB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Monoclonal
Conjugation
FITC
Isotype
IgG1
Purification
Purified by Protein G.
Size 1
100 µg
Tested Applications
WB, IHC, IF/ICC
Buffer
PBS, pH 7.4, 50% glycerol, 0.1% sodium azide.
Availability
Shipped within 5-12 working days.
Storage
Aliquot and store at 4°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q9BXM7-1
Gene ID
65018
NCBI Accession
NP_115785.1
OMIM
168600
Background
Antibody anti-PINK1
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

Related Products

EH15183

Human PINK1 (Serine/threonine-protein kinase PINK1, mitochondrial) ELISA Kit

Ver Producto
EM2190

Mouse PINK1(Serine/threonine-protein kinase PINK1, mitochondrial) ELISA Kit

Ver Producto
FNab09992

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