SIX Homeobox 1 Protein (SIX1) (His tag)

N° du produit ABIN5505772

Détail du produit

Antigène: SIX Homeobox 1 (SIX1)

Type de proteíne: Recombinant

Origine: Humain

Source: Escherichia coli (E. coli)

Purification/Conjugué: Cette SIX Homeobox 1 protéine est marqué à la His tag.

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

Attributs du produit:

• Recombinant human Purified recombinant protein of Human SIX homeobox 1 (SIX1), full length, with N-terminal HIS tag, expressed in E. coli, 50 μg (full length, N-term HIS tag) protein expressed in E.coli.
• Produced with end-sequenced ORF clone

Purification: Purified

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 N-terminal.

Restrictions: For Research Use only

Stockage

Concentration: 50 μg/mL

Buffer: 25 mM Tris, pH 8.0, 150 mM NaCl, 10 % glycerol, 1 % Sarkosyl.

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: SIX Homeobox 1 (SIX1)

Autre désignation: SIX homeobox 1 (SIX1 Produits)

Synonymes: BOS3 Protein, DFNA23 Protein, TIP39 Protein, BB138287 Protein, six1b Protein, six2 Protein, zgc:92332 Protein, XSix1 Protein, six1 Protein, zgc:77345 Protein, SIX homeobox 1 Protein, sine oculis-related homeobox 1 Protein, SIX homeobox 1a Protein, SIX homeobox 1 L homeolog Protein, SIX homeobox 1b Protein, SIX1 Protein, Six1 Protein, six1a Protein, six1.L Protein, six1b Protein

Sujet: The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3).

Poids moléculaire: 32 kDa

NCBI Accession: NP_005973

Pathways: Sensory Perception of Sound, Regulation of Muscle Cell Differentiation, Tube Formation, Skeletal Muscle Fiber Development