Homeobox D13 anticorps (N-Term)

N° du produit ABIN5516975

Détail du produit anti-Homeobox D13 anticorps

Antigène: Homeobox D13 (HOXD13)

Épitope: N-Term

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Homeobox D13 est non-conjugé

Application: Western Blotting (WB)

Séquence: ASGFAYPGTS ERTGSSSSSS SSAVVAARPE APPAKECPAP TPAAAAAAPP

Attributs du produit: This is a rabbit polyclonal antibody against HXD13. It was validated on Western Blot.

Purification: Affinity purified

Immunogène: The immunogen for Anti-HOXD13 antibody is: synthetic peptide directed towards the N-terminal region of Human HXD13

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur Homeobox D13

Antigène: Homeobox D13 (HOXD13)

Autre désignation: HOXD13 (HOXD13 Produits)

Synonymes: anticorps XHoxd13, anticorps BDE, anticorps BDSD, anticorps HOX4I, anticorps SPD, anticorps Hox-4.8, anticorps spdh, anticorps hoxd-13, anticorps hoxd13, anticorps zgc:110511, anticorps homeobox D13, anticorps homeobox D13 S homeolog, anticorps homeobox D13a, anticorps homeo box D13, anticorps HOXD13, anticorps hoxd13.S, anticorps Hoxd13, anticorps hoxd13a

Sujet: This gene belongs to the homeobox family of genes. The homeobox genes encode a highly conserved family of transcription factors that play an important role in morphogenesis in all multicellular organisms. Mammals possess four similar homeobox gene clusters, HOXA, HOXB, HOXC and HOXD, located on different chromosomes, consisting of 9 to 11 genes arranged in tandem. This gene is one of several homeobox HOXD genes located in a cluster on chromosome 2. Deletions that remove the entire HOXD gene cluster or the 5' end of this cluster have been associated with severe limb and genital abnormalities. Mutations in this particular gene cause synpolydactyly.

Alias Symbols: BDE, SPD, BDSD, HOX4I

Protein Size: 343

ID gène: 3239

NCBI Accession: NP_000514

UniProt: P35453

Pathways: Synaptic Membrane