Recombinant Anti-ALK-1 Antibody, Rabbit Monoclonal sinobiological 10066-R104

$1,900.00
In stock
SKU
10066-R104
Catalog No.SizePrice (USD)
10066-R104-11 mL$1,969.87
10066-R104-2020 µL$118.49
10066-R104-5050 µL$177.58
10066-R104-100100 µL$340.51

General Information

Product nameRecombinant Anti-ALK-1 Antibody, Rabbit Monoclonal
Validated applicationsELISA(Cap) (FAQ Protocol)
Species reactivityReacts with: Human
SpecificityHuman ALK-1
ImmunogenRecombinant Human ALK-1 / ACVRL1 Protein (Catalog#10066-H08H)
PreparationThis antibody was obtained from a rabbit immunized with purified, recombinant Human ALK-1 / ACVRL1 (rh ALK-1 / ACVRL1; Catalog#10066-H08H; NP_000011.2; Met1-Gln118).
SourceMonoclonal Rabbit IgG Clone #104
PurificationProtein A
Formulation0.2 μm filtered solution in PBS
ConjugateUnconjugated
FormLiquid
ShippingThis antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
StorageThis antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.

Synonyms: Anti-ACVRLK1 Antibody; Anti-ALK-1 Antibody; Anti-ALK1 Antibody; Anti-HHT Antibody; Anti-HHT2 Antibody; Anti-ORW2 Antibody; Anti-SKR3 Antibody; Anti-TSR-I Antibody

Background Information

Full Nameactivin A receptor type II-like 1
DescriptionActivin A receptor, type II-like 1 (ACVRL1), also known as ALK-1 (activin receptor-like kinase 1), is an endothelial-specific type I receptor of the TGF-beta (transforming growth factor beta) receptor family of ligands. On ligand binding, a heteromeric receptor complex forms consisting of two type II and two type I transmembrane serine/threonine kinases. ACVRL1 protein is expressed in certain blood vessels of kidney, spleen, heart and intestine, serving as an important role during vascular development. Mutations in ACVRL1 gene are associated with hemorrhagic telangiectasia type 2, also known as Rendu-Osler-Weber syndrome 2 and vascular disease.
References
  1. French Rendu-Osler network, et al. (2004) Molecular screening of ALK1/ACVRL1 and ENG genes in hereditary hemorrhagic telangiectasia in France. Hum Mutat. 23(4): 289-299.
  2. Simon M, et al. (2006) Association of a polymorphism of the ACVRL1 gene with sporadic arteriovenous malformations of the central nervous system. J Neurosurg. 104(6): 945-9.
  3. Argyriou L, et al. (2006) Novel mutations in the ENG and ACVRL1 genes causing hereditary hemorrhagic teleangiectasia. Int J Mol Med. 17(4):655-9.

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