Dynein Assembly Factor 4, Axonemal (DNAAF4) antibody

Catalog No. ABIN7468285

Product Details

Target: Dynein Assembly Factor 4, Axonemal (DNAAF4)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: Un-conjugated

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

Cross-Reactivity: Human

Purification: Purified by antigen-affinity chromatography.

Immunogen: Recombinant protein encompassing a sequence within the center region of human DYX1C1. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: A549 , H1299 , MCF-7

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details

Target: Dynein Assembly Factor 4, Axonemal (DNAAF4)

Alternative Name: dynein axonemal assembly factor 4

Synonyms: DYX1 antibody, DYXC1 antibody, EKN1 antibody, RD antibody, dynein axonemal assembly factor 4 antibody, DNAAF4 antibody

Background:

Synonyms: dynein axonemal assembly factor 4 , CILD25 , DYX1 , DYX1C1 , DYXC1 , EKN1 , RD

Background: This gene encodes a tetratricopeptide repeat domain-containing protein. The encoded protein interacts with estrogen receptors and the heat shock proteins, Hsp70 and Hsp90. A chromosomal translocation involving this gene is associated with a susceptibility to developmental dyslexia. Mutations in this gene are associated with deficits in reading and spelling. Alternate splicing results in multiple transcript variants. [provided by RefSeq]

Molecular Weight: 49 kDa

Gene ID: 161582

UniProt: Q8WXU2