FAST Kinase Domain-Containing Protein 2, Mitochondrial (FASTKD2) Antibody

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208€ (20 µl)

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935106861
info@markelab.com
name
FAST Kinase Domain-Containing Protein 2, Mitochondrial (FASTKD2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx004579
tested applications
WB, IF/ICC

Description

FASTKD2 Antibody is a Rabbit Polyclonal antibody against FASTKD2. This gene encodes a protein that is localized in the mitochondrial inner compartment and that may play a role in mitochondrial apoptosis. Nonsense mutations have been reported to result in cytochrome c oxidase deficiency.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Target: FAST Kinase Domain-Containing Protein 2, Mitochondrial (FASTKD2)
Immunogen: Synthetic peptide corresponding to FASTKD2. The exact sequence is proprietary.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Assay Type
Concentration: > 0.2 mg/ml
Recommended Dilution
WB: 1/500 - 1/1000, IF/ICC: 1/50 - 1/200. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Observed MW
Calculated MW: 33 kDa  Observed MW: 45 kDa
Purification
Purified by affinity chromatography.
Size 1
20 µl
Size 2
100 µl
Size 3
2 × 100 µl
Form
Liquid
Tested Applications
WB, IF/ICC
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 0.05% BSA, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q9NYY8
Gene ID
22868
OMIM
612322
Background
Antibody anti-FASTKD2
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

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FAST Kinase Domain-Containing Protein 2, Mitochondrial (FASTKD2) Antibody

FASTKD2 Antibody is a Rabbit Polyclonal antibody against FASTKD2. This gene encodes a protein that is localized in the mitochondrial inner compartment and that may play a role in mitochondrial apoptosis. Nonsense mutations have been reported to result in cytochrome c oxidase deficiency.

Ver Producto