Dnah5 anticorps (AA 400-650)

N° du produit ABIN7266861

Cet anticorps anti-Dnah5 est un anticorps Lapin Polyclonal détectant Dnah5 dans WB. Adapté pour Humain.

Aperçu rapide pour Dnah5 anticorps (AA 400-650) (ABIN7266861)

Antigène: Dnah5 (Dynein, Axonemal, Heavy Chain 5 (Dnah5))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Dnah5 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Dnah5 anticorps

Épitope: AA 400-650

Fonction: DNAH5 Rabbit pAb

Séquence: VTNQIISACK AYITNNGTAS IWNQPQDVVE EKILSAIKLK QEYQLCFHKT KQKLKQNPNA KQFDFSEMYI FGKFETFHRR LAKIIDIFTT LKTYSVLQDS TIEGLEDMAT KYQGIVATIK KKEYNFLDQR KMDFDQDYEE FCKQTNDLHN ELRKFMDVTF AKIQNTNQAL RMLKKFERLN IPNLGIDDKY QLILENYGAD IDMISKLYTK QKYDPPLARN QPPIAGKILW ARQLFHRIQQ PMQLFQQHPA V

Réactivité croisée: Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 400-650 of human DNAH5 (NP_001360.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

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. Avoid freeze / thaw cycles.

Détails sur Dnah5

Antigène: Dnah5 (Dynein, Axonemal, Heavy Chain 5 (Dnah5))

Autre désignation: DNAH5

Sujet: This gene encodes a dynein protein, which is part of a microtubule-associated motor protein complex consisting of heavy, light, and intermediate chains. This protein is an axonemal heavy chain dynein. It functions as a force-generating protein with ATPase activity, whereby the release of ADP is thought to produce the force-producing power stroke. Mutations in this gene cause primary ciliary dyskinesia type 3, as well as Kartagener syndrome, which are both diseases due to ciliary defects. [provided by RefSeq, Oct 2009],CILD3,DNAHC5,HL1,KTGNR,PCD,DNAH5,Signal Transduction,Cell Biology & Developmental Biology,Cytoskeleton,Motor Proteins,DNAH5

ID gène: 1767

UniProt: Q8TE73