Amphoterin-Induced Protein 1 (AMIGO-1) Antibody (HRP)

Este producto es parte de AMIGO - Amphoterin-induced protein
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624€ (100 µg)

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935106861
info@markelab.com
name
Amphoterin-Induced Protein 1 (AMIGO-1) Antibody (HRP)
category
Primary Antibodies
provider
Abbexa
reference
abx443568
tested applications
WB, IHC, IF/ICC

Description

AMIGO-1 Antibody is a Mouse Monoclonal against AMIGO1.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetAmphoterin-Induced Protein 1 (AMIGO-1)
HostMouse
ReactivityHuman, Mouse, Rat
Recommended DilutionWB: 1/1000. Optimal dilutions/concentrations should be determined by the end user.
ClonalityMonoclonal
ConjugationHRP
IsotypeIgG1
PurificationPurified by Protein G.
Size 1100 µg
Tested ApplicationsWB, IHC, IF/ICC
BufferPBS, pH 7.4, 50% glycerol, 0.09% sodium azide.
AvailabilityShipped within 5-12 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
UniProt IDQ86WK6
Gene ID57463
NCBI AccessionNP_065754.2
AliasAMIGO-1,Alivin-2
BackgroundAntibody anti-AMIGO1
StatusRUO
NoteConcentration: 1 mg/ml -

Descripción

AMIGO1 is a cell adhesion molecule belonging to the AMIGO family, which is involved in neuronal development, axon guidance, and synaptic formation. AMIGO1 is highly expressed in the central nervous system (CNS), where it mediates neurite outgrowth and contributes to axon fasciculation during neural circuit formation. It interacts with other cell adhesion molecules and extracellular matrix proteins to promote cell-cell and cell-extracellular interactions critical for proper neuronal connectivity. AMIGO1 has also been implicated in synaptic plasticity and stability, supporting learning, memory, and neural repair. Dysregulation of AMIGO1 has been associated with neurodegenerative diseases such as Alzheimer’s disease, where axonal damage and synaptic dysfunction are observed. In addition to its neuronal roles, emerging evidence suggests that AMIGO1 may influence tumor progression, as its expression can promote cell migration and invasion in certain cancers. This highlights its dual significance in both neural development and disease pathology.

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