FERMT3 Protein (Myc-DYKDDDDK Tag)

Produktnummer ABIN2721017

Produktdetails

Target: FERMT3 (Fermitin Family Member 3 (FERMT3))

Protein-Typ: Recombinant

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses FERMT3 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human FERMT3 (transcript variant URP2SF) protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.

Antigendetails

Target: FERMT3 (Fermitin Family Member 3 (FERMT3))

Andere Bezeichnung: Fermt3 (FERMT3 Produkte)

Synonyme: C79673 Protein, Kindlin3 Protein, RGD1310168 Protein, MGC69069 Protein, MGC88900 Protein, KIND3 Protein, MIG-2 Protein, MIG2B Protein, UNC112C Protein, URP2 Protein, URP2SF Protein, zgc:64101 Protein, fermitin family member 3 Protein, fermitin family member 3 L homeolog Protein, fermitin family member 3b Protein, Fermt3 Protein, fermt3.L Protein, fermt3 Protein, FERMT3 Protein, fermt3b Protein

Hintergrund: Kindlins are a small family of proteins that mediate protein-protein interactions involved in integrin activation and thereby have a role in cell adhesion, migration, differentiation, and proliferation. The protein encoded by this gene has a key role in the regulation of hemostasis and thrombosis. This protein may also help maintain the membrane skeleton of erythrocytes. Mutations in this gene cause the autosomal recessive leukocyte adhesion deficiency syndrome-III (LAD-III). Alternative splicing results in multiple transcript variants encoding distinct isoforms.

Molekulargewicht: 75.2 kDa

NCBI Accession: NP_113659