DLX3 Protein (AA 1-186) (His tag)

N° du produit ABIN5853443

Détail du produit

Antigène: DLX3 (Distal-Less Homeobox 3 (DLX3))

Type de proteíne: Recombinant

Attributs du protein: AA 1-186

Origine: Humain

Source: Escherichia coli (E. coli)

Purification/Conjugué: Cette DLX3 protéine est marqué à la His tag.

Application: SDS-PAGE (SDS)

Séquence: MGSSHHHHHH SSGLVPRGSH MGSMSGSFDR KLSSILTDIS SSLSCHAGSK DSPTLPESSV TDLGYYSAPQ HDYYSGQPYG QTVNPYTYHH QFNLNGLAGT GAYSPKSEYT YGASYRQYGA YREQPLPAQD PVSVKEEPEA EVRMVNGKPK KVRKPRTIYS SYQLAALQRR FQKAQYLALP ERAELAAQLG LTQTQVKIWF QNRRSKFKK

Pureté: > 90 % by SDS - PAGE

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

Denatured

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid. In 20  mM Tris-HCl buffer (  pH 8.0) containing 10 % glycerol

Stock: 4 °C,-20 °C,-80 °C

Stockage commentaire: Can be stored at +4C short term (1-2 weeks). For long term storage, aliquot and store at -20C or -70C. Avoid repeated freezing and thawing cycles.

Détail du antigène

Antigène: DLX3 (Distal-Less Homeobox 3 (DLX3))

Autre désignation: DLX3 (DLX3 Produits)

Synonymes: AI4 Protein, TDO Protein, AV237891 Protein, Dlx-3 Protein, DLX3 Protein, ai4 Protein, tdo Protein, xdlx3 Protein, MGC69301 Protein, dll2 Protein, dlx3 Protein, dlx-3 Protein, id:ibd3531 Protein, wu:fb83f11 Protein, zgc:91827 Protein, distal-less homeobox 3 Protein, distal-less homeobox 3 L homeolog Protein, distal-less homeobox 3b Protein, DLX3 Protein, Dlx3 Protein, dlx3 Protein, dlx3.L Protein, dlx3b Protein

Sujet: Many vertebrate homeo box-containing genes have been identified on the basis of their sequence similarity with Drosophila developmental genes. Members of the Dlx gene family contain a homeobox that is related to that of Distal-less (Dll), a gene expressed in the head and limbs of the developing fruit fly. The Distal-less (Dlx) family of genes comprises at least 6 different members, DLX1-DLX6. Trichodentoosseous syndrome (TDO), an autosomal dominant condition, has been correlated with DLX3 gene mutation. This gene is located in a tail-to-tail configuration with another member of the gene family on the long arm of chromosome 17. Mutations in DLX3 have been associated with the autosomal dominant conditions trichodentoosseous syndrome and amelogenesis imperfecta with taurodontism. Recombinant human DLX3 protein, fused to His-tag at N-terminus, was expressed in E.coli.

Poids moléculaire: 23.4kDa (209aa)

NCBI Accession: NP_005211

UniProt: O60479