Homeobox D13 anticorps (AA 251-343)

N° du produit ABIN1387917

Cet anticorps anti-Homeobox D13 est un anticorps Lapin Polyclonal détectant Homeobox D13 dans WB, ELISA, IHC (p), ICC, IF (cc), IF (p) et IHC (fro). Adapté pour Humain.

Aperçu rapide pour Homeobox D13 anticorps (AA 251-343) (ABIN1387917)

Antigène: Homeobox D13 (HOXD13)

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Homeobox D13 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-Homeobox D13 anticorps

Épitope: AA 251-343

Homologie: Human,Mouse,Rat,Cow,Sheep,Pig,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human HOXD13

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.

Agent conservateur: ProClin

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

Stock: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur Homeobox D13

Antigène: Homeobox D13 (HOXD13)

Autre désignation: HOXD13

Sujet:

Synonyms: HOXD13, BDE, BDSD, Homeo box 4I, Homeo box D13, Homeo box protein Hox D13, Homeo box protein HoxD13, Homeobox 4I, Homeobox D13, Homeobox protein Hox D13, Homeobox protein Hox-D13, Homeobox protein HoxD13, Homeobox4I, HomeoboxD13, Hox 4I, HOX D13, Hox-4.8, Hox4I, HOXD 13, HoxD13, SPD, HXD13_HUMAN.

Background: The Hox proteins play a role in development and cellular differentiation by regulating downstream target genes. Specifically, the Hox proteins direct DNA-protein and protein-protein interactions that assist in determining the morphologic features associated with the anterior-posterior body axis. HoxD13 is a sequence-specific transcription factor that provides cells with specific positional identities on the anterior-posterior axis of developing mammals. Defects in HoxD13 are the cause of synpolydactyly (SPD). SPD is a limb malformation that shows a characteristic manifestation in both hands and feet. This condition is inherited as an autosomal dominant trait with reduced penetrance. Defects in HoxD13 are also the cause of brachydactyly type D and type E.

ID gène: 3239

Pathways: Synaptic Membrane