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Recombinant Human Stra6 Protein (RMPP-00230718)

Cat. No.: RMPP-00230718

Category: Actin Binding Proteins

Research Area: Signal Transduction

INQUIRY 2 μg Customer Size

Product Features

Source HEK 293 cells
Purity > 97% SDS-PAGE.
Nature Recombinant
Endotoxin Level < 1.000 Eu/µg
Animal Free No
Tags His tag C-Terminus, Fc tag C-Terminus
Form Lyophilized
Applications SDS-PAGE; Functional Studies
Key Features Expression system: HEK 293 cells; Purity: > 97% SDS-PAGE; Endotoxin level: < 1.000 Eu/µg; Active: Yes; Tags: His tag C-Terminus, Fc tag C-Terminus; Suitable for: SDS-PAGE, Functional Studies

Protein Information

UniProt ID Q13705
Molecular Weight 41 kDa including tags
Molecular Weight Information The recombinant mouse ACVR2B/Fc is a disulfide-linked homodimer after removal of the signal peptide. The reduced monomer consists of 364 amino acids and has a predicted molecular mass of 41 kDa. In SDS-PAGE under reducing conditions, the apparent molecular mass of rmACVR2B/Fc monomer is approximately 60-65 kDa due to glycosylation.
Sequence MTAPWAALAL LWGSLCAGSG RGEAETRECI YYNANWELER TNQSGLERCE GEQDKRLHCY ASWRNSSGTI ELVKKGCWLD DFNCYDRQEC VATEENPQVY FCCCEGNFCN ERFTHLPEPG GPEVTYEPPP TAPT
Sequence Similarities Belongs to the protein kinase superfamily. TKL Ser/Thr protein kinase family. TGFB receptor subfamily. Contains 1 protein kinase domain.
Protein Length Protein fragment
Cellular Localization Membrane.
Function On ligand binding, forms a receptor complex consisting of two type II and two type I transmembrane serine/threonine kinases. Type II receptors phosphorylate and activate type I receptors which autophosphorylate, then bind and activate SMAD transcriptional regulators. Receptor for activin A, activin B and inhibin A.
Involvement in Disease Defects in ACVR2B are the cause of visceral heterotaxy autosomal type 4 (HTX4). A form of visceral heterotaxy, a complex disorder due to disruption of the normal left-right asymmetry of the thoracoabdominal organs. It results in anthis product arrangement of visceral organs, and a wide variety of congenital defects. Clinical features of visceral heterotaxy type 4 include dextrocardia, right aortic arch and a right-sided spleen, anomalies of the inferior and the superior vena cava, atrial ventricular canal defect with dextro-transposed great arteries, pulmonary stenosis, polysplenia and midline liver.

Storage & Shipping

Shipping and Storage Shipped at Room Temperature. Upon delivery aliquot. Store at -20°C or -80°C. Avoid freeze / thaw cycle.
pH: 7.40Constituent: 100% PBS
This product is an active protein and may elicit a biological response in vivo, handle with caution.

For research use only. Not for clinical use.