MKS1 anticorps

N° du produit ABIN6263271

Détail du produit anti-MKS1 anticorps

Antigène: MKS1 (Meckel Syndrome, Type 1 (MKS1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MKS1 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC)

Specificité: MKS1 antibody detects endogenous levels of MKS1.

Réactivité croisée: Humain, Souris, Rat (Rattus)

Purification: The antiserum was purified by peptide affinity chromatography using SulfoLink^TM Coupling Resin (Thermo Fisher Scientific).

Immunogène: A synthesized peptide derived from human MKS1.

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:2000, IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: Rabbit IgG in phosphate buffered saline ,  pH 7.4, 150  mM NaCl, 0.02 % sodium azide and 50 % glycerol.

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: Store at -20 °C.Stable for 12 months from date of receipt

Date de péremption: 12 months

Détails sur MKS1

Antigène: MKS1 (Meckel Syndrome, Type 1 (MKS1))

Autre désignation: MKS1 (MKS1 Produits)

Synonymes: anticorps BBS13, anticorps MES, anticorps MKS, anticorps POC12, anticorps AK190930, anticorps B8d3, anticorps Meckel syndrome, type 1, anticorps MKS1, anticorps Mks1

Sujet:

Description: Component of the tectonic-like complex, a complex localized at the transition zone of primary cilia and acting as a barrier that prevents diffusion of transmembrane proteins between the cilia and plasma membranes. Involved in centrosome migration to the apical cell surface during early ciliogenesis. Required for ciliary structure and function, including a role in regulating length and appropriate number through modulating centrosome duplication. Required for cell branching morphology.

Gene: MKS1

Poids moléculaire: 65-70 kDa

ID gène: 54903

UniProt: Q9NXB0