Microfibrillar Associated Protein 2 (MFAP2) Antibody

Este producto es parte de MFAP - microfibril associated protein
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286€ (100 µl)

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935106861
info@markelab.com
name
Microfibrillar Associated Protein 2 (MFAP2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx128849
tested applications
WB, IHC, IF/ICC

Description

Microfibrillar Associated Protein 2 Antibody is a Rabbit Polyclonal against Microfibrillar Associated Protein 2.

Documents del producto

Instrucciones
Data sheet
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Product specifications

CategoryPrimary Antibodies
Immunogen TargetMicrofibrillar Associated Protein 2 (MFAP2)
HostRabbit
ReactivityHuman
Recommended DilutionWB: 0.01-2 µg/ml, IHC: 5-20 µg/ml, IF/ICC: 5-20 µg/ml. Optimal dilutions/concentrations should be determined by the end user.
ClonalityPolyclonal
ConjugationUnconjugated
PurificationPurified by antigen-specific affinity chromatography, followed by Protein A affinity chromatography.
Size 1100 µl
Size 2200 µl
Size 31 ml
FormLiquid
Tested ApplicationsWB, IHC, IF/ICC
Buffer0.01 M PBS, pH 7.4, containing 0.05% Proclin-300, 50% glycerol.
AvailabilityShipped within 5-7 working days.
StorageAliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry IceNo
AliasMAGP,MAGP1,MAGP-1,MFAP-2
BackgroundAntibody anti-MFAP2
StatusRUO

Descripción

Microfibril Associated Protein 2 (MFAP2), also known as MAGP-1, is a component of the extracellular matrix associated with microfibrils. MFAP2 interacts with fibrillin and elastin to contribute to the structural integrity and elastic properties of connective tissues. It plays a role in modulating signaling pathways such as TGF-β and BMP, which are crucial for tissue homeostasis, repair, and development. Dysregulation of MFAP2 has been implicated in connective tissue disorders, including Marfan syndrome and aortic aneurysms, due to its impact on microfibril assembly and extracellular matrix stability. MFAP2 also has emerging roles in angiogenesis and tumor progression, where it influences the extracellular microenvironment and cell signaling.

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