T-Box 5 anticorps

N° du produit ABIN2460713

Détail du produit anti-T-Box 5 anticorps

Antigène: T-Box 5 (TBX5)

Reactivité: Humain, Chien

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp T-Box 5 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (IHC)

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human TBX5.

Information d'application

Indications d'application: TBX5 antibody can be used for detection of TBX5 by ELISA at 1:62500. TBX5 antibody can be used for detection of TBX5 by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store TBX5 antibody at -20 °C.

Détails sur T-Box 5

Antigène: T-Box 5 (TBX5)

Autre désignation: TBX5 (TBX5 Produits)

Synonymes: anticorps TBX5, anticorps tbx-5, anticorps xtbx-5, anticorps xtbx5, anticorps tbx5, anticorps HOS, anticorps tbx5.1, anticorps zTbx5, anticorps zf-tbx5, anticorps T-box 5, anticorps T-box 5 L homeolog, anticorps T-box 5a, anticorps TBX5, anticorps tbx5, anticorps tbx5.L, anticorps Tbx5, anticorps tbx5a

Sujet: TBX5 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12. The encoded protein may play a role in heart development and specification of limb identity. Mutations in this gene have been associated with Holt-Oram syndrome, a developmental disorder affecting the heart and upper limbs.

Poids moléculaire: 39 kDa

ID gène: 6910

NCBI Accession: NP_542449

UniProt: Q99593