A Kinase Anchor Protein 17A (AKAP17A) Antibody (FITC)

Este producto es parte de AKAP - A kinase anchor protein
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169€ (20 µg)

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935106861
info@markelab.com
name
A Kinase Anchor Protein 17A (AKAP17A) Antibody (FITC)
category
Primary Antibodies
provider
Abbexa
reference
abx315370

Description

AKAP17A Antibody (FITC) is a Rabbit Polyclonal against AKAP17A conjugated to FITC.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
A Kinase Anchor Protein 17A (AKAP17A)
Host
Rabbit
Reactivity
Human
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
FITC
Isotype
IgG
Purity
> 95%
Purification
Purified by Protein G.
Size 1
20 µg
Size 2
50 µg
Size 3
100 µg
Size 4
200 µg
Size 5
1 mg
Form
Liquid
Buffer
0.01 M PBS, pH 7.4, 0.03% Proclin-300 and 50% Glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid exposure to light. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q02040
Gene ID
8227
NCBI Accession
NP_005079.2, NM_005088.2
OMIM
312095
Alias
721P,AKAP-17A,CCDC133
Background
Antibody anti-AKAP17A
Status
RUO

Descripción

AKAP17A, also known as S-AKAP84, is a mitochondrial scaffold protein that binds PKA and regulates mitochondrial function, including ATP production and apoptosis. AKAP17A primarily anchors PKA to the mitochondrial membrane, facilitating cAMP-dependent signaling pathways that control oxidative phosphorylation and energy homeostasis. It has a role in maintaining mitochondrial integrity during cellular stress by regulating apoptosis signaling, including interactions with pro- and anti-apoptotic proteins like Bcl-2 and caspases. AKAP17A is expressed in tissues with high energy demands, such as cardiac and skeletal muscle, where it enhances mitochondrial respiration. Dysregulation of AKAP17A impairs mitochondrial dynamics, contributing to metabolic disorders, neurodegeneration, and cardiovascular diseases. AKAP17A has also been shown to interact with mitochondrial DNA-binding proteins, influencing mitochondrial biogenesis and replication under stress conditions.

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