Homeobox D13 anticorps (AA 202-230)

N° du produit ABIN5536745

Détail du produit anti-Homeobox D13 anticorps

Antigène: Homeobox D13 (HOXD13)

Épitope: AA 202-230

Reactivité: Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Homeobox D13 est non-conjugé

Application: Western Blotting (WB)

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: For WB starting dilution is: 1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.36 mg/mL

Buffer: 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: Store at 4°C for three months and -20°C, stable for up to one year. As with all antibodies care should be taken to avoid repeated freeze thaw cycles. Antibodies should not be exposed to prolonged high temperatures.

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.

Poids moléculaire: 36 kDa

ID gène: 3239

UniProt: P35453

Pathways: Synaptic Membrane