FERMT3 Protein (Myc-DYKDDDDK Tag)

N° du produit ABIN2721017

Détail du produit

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

Type de proteíne: Recombinant

Origine: Humain

Source: HEK-293 Cells

Purification/Conjugué: Cette FERMT3 protéine est marqué à la Myc-DYKDDDDK Tag.

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

Attributs du produit:

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

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

Information d'application

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

Commentaires:

The tag is located at the C-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

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

Stock: -80 °C

Stockage commentaire: 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.

Détail du antigène

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

Autre désignation: Fermt3 (FERMT3 Produits)

Synonymes: 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

Sujet: 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.

Poids moléculaire: 75.2 kDa

NCBI Accession: NP_113659