MSX1 anticorps (AA 111-138)

N° du produit ABIN5536284

Détail du produit anti-MSX1 anticorps

Antigène: MSX1 (Msh Homeobox 1 (MSX1))

Épitope: AA 111-138

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MSX1 est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF)

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

Immunogène: This MSX1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 111-138 amino acids from the Central region of human MSX1.

Isotype: Ig Fraction

Information d'application

Indications d'application: For WB starting dilution is: 1:2000

For IF starting dilution is: 1:10~50

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.48 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 MSX1

Antigène: MSX1 (Msh Homeobox 1 (MSX1))

Autre désignation: MSX1 (MSX1 Produits)

Synonymes: anticorps ECTD3, anticorps HOX7, anticorps HYD1, anticorps STHAG1, anticorps AA675338, anticorps AI324650, anticorps Hox-7, anticorps Hox7, anticorps Hox7.1, anticorps msh, anticorps CHOX-7, anticorps GHOX-7, anticorps HOX-7, anticorps msh homeobox 1, anticorps MSX1, anticorps Msx1

Sujet: This gene encodes a member of the muscle segment homeobox gene family. The encoded protein functions as a transcriptional repressor during embryogenesis through interactions with components of the core transcription complex and other homeoproteins. It may also have roles in limb-pattern formation, craniofacial development, particularly odontogenesis, and tumor growth inhibition. Mutations in this gene, which was once known as homeobox 7, have been associated with nonsyndromic cleft lip with or without cleft palate 5, Witkop syndrome, Wolf-Hirschom syndrome, and autosomoal dominant hypodontia.

Poids moléculaire: 31 kDa

ID gène: 4487

UniProt: P28360

Pathways: Regulation of Muscle Cell Differentiation, Positive Regulation of Response to DNA Damage Stimulus