Acylphosphatase 1, Erythrocyte (ACYP1) Antibody

Este producto es parte de ACYP - Acylphosphatase
Acylphosphatase 1, Erythrocyte (ACYP1) Antibody
637€ (100 µl)

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Name
Acylphosphatase 1, Erythrocyte (ACYP1) Antibody
Category
Primary Antibodies
Provider
Abbexa
Reference
abx110816
Tested Applications
ELISA, WB

Description

Acylphosphatase 1, Erythrocyte (Common) Type Antibody is a Rabbit Polyclonal antibody against Acylphosphatase 1, Erythrocyte (Common) Type.

Documentos del producto

Instrucciones
Data sheet
Descargar

Especificaciones del producto

Category
Primary Antibodies
Immunogen Target
Target: Acylphosphatase 1, Erythrocyte (ACYP1)
Immunogen: Human ACYP1.
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Antigen Affinity Chromatography.
Size 1
100 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS, pH 7.3, containing 0.1% Sodium Azide and 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
P07311
Gene ID
97
NCBI Accession
NP_001098.1, NM_001107.4
OMIM
600875
Alias
erythrocyte isozyme,Acylphosphate phosphohydrolase 1
Background
Antibody anti-ACYP1
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.

Background

Acylphosphatase 1 (ACYP1) is a small cytosolic enzyme that catalyzes the hydrolysis of acyl-phosphate bonds in a variety of substrates, including 1,3-bisphosphoglycerate and carbamoyl phosphate. ACYP1 is primarily expressed in erythrocytes and the brain, where it is thought to play a role in maintaining energy homeostasis and regulating cellular metabolism. It may also influence signaling pathways by modulating the levels of phosphorylated intermediates. ACYP1 has been implicated in oxidative stress responses and apoptosis, as its dysregulation is associated with increased susceptibility to oxidative damage. Mutations or altered expression of ACYP1 may contribute to neurological disorders and metabolic diseases, though its precise physiological roles remain under investigation.

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