Dnah5 antibody (AA 400-650)

Catalog No. ABIN7266861

This anti-Dnah5 antibody is a Rabbit Polyclonal antibody detecting Dnah5 in WB. Suitable for Human.

Quick Overview for Dnah5 antibody (AA 400-650) (ABIN7266861)

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

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This Dnah5 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-Dnah5 Antibody

Binding Specificity: AA 400-650

Purpose: DNAH5 Rabbit pAb

Sequence: 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

Cross-Reactivity: Mouse, Rat

Characteristics: Polyclonal Antibodies

Purification: Affinity purification

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

Isotype: IgG

Application Details

Application Notes: WB,1:500 - 1:2000

Restrictions: For Research Use only

Handling

Format: Liquid

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

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Avoid freeze / thaw cycles.

Target Details for Dnah5

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

Alternative Name: DNAH5

Background: 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

Gene ID: 1767

UniProt: Q8TE73