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Merck
CN

A1229

Sigma-Aldrich

Angiopoietin-3 from mouse

recombinant, expressed in NSO cells, ≥90% (SDS-PAGE), lyophilized powder

Synonym(s):

ANG-3

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About This Item

MDL number:
MFCD06798419
UNSPSC Code:
51111800

Key Documents

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biological source

mouse

recombinant

expressed in NSO cells

Assay

≥90% (SDS-PAGE)

form

lyophilized powder

mol wt

apparent mol wt 85-90 kDa by SDS-PAGE (reducing)
calculated mol wt ~58 kDa

storage condition

avoid repeated freeze/thaw cycles (Do not store in a frost-free freezer.)

impurities

endotoxin, tested

UniProt accession no.

Q9WVH6

storage temp.

−20°C

Gene Information

mouse ... Angptl1(72713)

Physical form

Lyophilized from a 0.2 μm filtered solution in 50 mM Tris citrate and 0.5 M sodium chloride, pH 6.5, containing 1.25 mg bovine serum albumin.

Analysis Note

The biological activity is measured by its ability to bind immobilized Tie-2/Fc in ELISA.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
084K0894

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K Teichert-Kuliszewska et al.
Cardiovascular research, 49(3), 659-670 (2001-02-13)
The endothelial cell (EC) specific tyrosine kinase receptor, Tie2, interacts with at least two ligands, angiopoietin-1 (Ang1) and angiopoietin-2 (Ang2). Ang1 stimulates Tie2 receptor autophosphorylation, while Ang2 has been reported to inhibit Ang1-induced Tie2 receptor autophosphorylation. We studied the effects
D M Valenzuela et al.
Proceedings of the National Academy of Sciences of the United States of America, 96(5), 1904-1909 (1999-03-03)
The angiopoietins have recently joined the members of the vascular endothelial growth factor family as the only known growth factors largely specific for vascular endothelium. The angiopoietins include a naturally occurring agonist, angiopoietin-1, as well as a naturally occurring antagonist
Sameer S Udhane et al.
Scientific reports, 5, 10132-10132 (2015-05-15)
Androgens are essential for sexual development and reproduction. However, androgen regulation in health and disease is poorly understood. We showed that human adrenocortical H295R cells grown under starvation conditions acquire a hyperandrogenic steroid profile with changes in steroid metabolizing enzymes

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