Homeobox D13 anticorps (AA 202-230)

N° du produit ABIN655171

Cet anticorps Lapin Polyclonal détecte spécifiquement Homeobox D13 dans WB. Il présente une réactivité envers Souris.

Aperçu rapide pour Homeobox D13 anticorps (AA 202-230) (ABIN655171)

Antigène: Homeobox D13 (HOXD13)

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Homeobox D13 est non-conjugé

Application: Western Blotting (WB)

Clone: RB19191

Détail du produit anti-Homeobox D13 anticorps

Épitope: AA 202-230

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This HOXD13 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 202-230 amino acids from the Central region of human HOXD13.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

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: 4 °C,-20 °C

Stockage commentaire: Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Date de péremption: 6 months

Détails sur Homeobox D13

Antigène: Homeobox D13 (HOXD13)

Autre désignation: HOXD13

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.

Poids moléculaire: 36101

ID gène: 3239

NCBI Accession: NP_000514

UniProt: P35453

Pathways: Synaptic Membrane