Mouse Serine/threonine-Protein Kinase Receptor R3 (ACVRL1) Protein (Active)

Este producto es parte de ACVR - Activin A Receptor Type
Mouse Serine/threonine-Protein Kinase Receptor R3 (ACVRL1) Protein (Active)
1638€ (200 µg)

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Name
Mouse Serine/threonine-Protein Kinase Receptor R3 (ACVRL1) Protein (Active)
Category
Proteins and Peptides
Provider
Abbexa
Reference
abx692709
Tested Applications
SDS-PAGE

Description

Mouse ALK-1 Protein is a recombinant protein from Mouse produced in HEK293 Cells. A DNA sequence encoding the mouse ALK1 (NP_033742.2) precursor (Met 1-Pro 119) was fused with the C-terminal polyhistidine-tagged Fc region of human IgG1 at the C-terminus.

Documentos del producto

Instrucciones
Data sheet
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Especificaciones del producto

Category
Proteins and Peptides
Immunogen Target
ALK-1
Host
HEK293 cells
Assay Type
Activity: Active
Sequence Fragment: Met1-Pro119
Tag: C-terminal His tag and Fc tag
Origin
Mouse
Observed MW
39 kDa
Expression
Recombinant
Purity
> 95% (SDS-PAGE)
Size 1
200 µg
Form
Lyophilized
Tested Applications
SDS-PAGE
Buffer
Lyophilized from sterile PBS, pH 7.4.
Availability
Shipped within 5-15 working days.
Storage
Storage: Store lyophilized between -20 °C and -80°C.
Stability: Stable when stored reconstituted at 2-8°C for up to 1 week. Reconstituted aliquots are stable at -20°C for up to 3 months.
Shelf Life: 12 months.
Dry Ice
No
NCBI Accession
NP_033742.2
Alias
Activin receptor-like kinase 1,ALK-1,SKR3
Background
Protein ACVRL1
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.
Endotoxin Level: < 1.0 EU per µg of the protein as determined by the LAL method.

Background

ACVRL1, also known as ALK1, is a type I receptor that primarily binds BMP9 and BMP10. It is critical for vascular development and endothelial cell function. ACVRL1 regulates angiogenesis through the SMAD1/5/8 signaling pathway, promoting endothelial proliferation and vessel stability. Mutations in ACVRL1 cause hereditary hemorrhagic telangiectasia (HHT), a genetic disorder characterized by abnormal blood vessel formation and recurrent bleeding. It is primarily expressed in vascular endothelial cells.

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