MKKS anticorps

N° du produit ABIN7074572

Détail du produit anti-MKKS anticorps

Antigène: MKKS (McKusick-Kaufman Syndrome (MKKS))

Reactivité: Humain, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MKKS est non-conjugé

Application: Western Blotting (WB)

Réactivité croisée: Humain, Rat

Purification: Affinity purification

Immunogène: Recombinant protein corresponding to Mouse MKKS

Information d'application

Indications d'application: WB (H,R) 1:1000-1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS, pH 7.4, 0.02 % 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: -20 °C

Détails sur MKKS

Antigène: MKKS (McKusick-Kaufman Syndrome (MKKS))

Autre désignation: MKKS (MKKS Produits)

Synonymes: anticorps bbs6, anticorps zgc:55608, anticorps MKKS, anticorps kms, anticorps mks, anticorps hmcs, anticorps DKFZp459L0833, anticorps BBS6, anticorps HMCS, anticorps KMS, anticorps MKS, anticorps 1300013E18Rik, anticorps AI463362, anticorps AI957237, anticorps Bbs6, anticorps McKusick-Kaufman syndrome, anticorps Mkks, anticorps mkks, anticorps MKKS

Sujet: MKKS also known as BBS6 is a probable chaperone given to the amino acid similarity to the chaperonin family of proteins and may play a role in protein processing in limb, cardiac and reproductive system development. The mutations in BBS6 have been linked to Bardet-Biedl syndrome (BBS) which is a genetically heterogeneous, autosomal recessive disorder characterized by usually severe pigmentary retinopathy, early onset obesity, polydactyly, hypogenitalism, renal malformation and mental retardation. It may also get involved in cellular organization processes, in particular relating to ciliary/flagellar and centrosomal activities.

Poids moléculaire: 62 kDa

ID gène: 59030

NCBI Accession: NP_001135418

UniProt: Q9JI70

Pathways: Sensory Perception of Sound