ARG64531

anti-DYX1C1 / EKN1 antibody

anti-DYX1C1 / EKN1 antibody for Western blot and Human

Controls and Markers antibody; Neuroscience antibody

Overview

Product Description Goat Polyclonal antibody recognizes DYX1C1 / EKN1
Tested Reactivity Hu
Predict Reactivity Dog
Tested Application WB
Specificity This antibody is expected to recognise three reported isoforms (NP_570722.2, NP_001028731.1 and NP_001028732.1).
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name DYX1C1 / EKN1
Antigen Species Human
Immunogen PLQVSDYSWQQTKT-C
Conjugation Un-conjugated
Alternate Names DYX1; CILD25; Dyslexia susceptibility 1 candidate gene 1 protein; RD; EKN1; DYXC1; DNAAF4

Application Instructions

Application Suggestion
Tested Application Dilution
WB0.5 - 1.5 µg/ml
Application Note WB: Recommend incubate at RT for 1h.
* The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Buffer Tris saline (pH 7.3), 0.02% Sodium azide and 0.5% BSA
Preservative 0.02% Sodium azide
Stabilizer 0.5% BSA
Concentration 0.5 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 161582 Human DYX1C1

Swiss-port # Q8WXU2 Human Dyslexia susceptibility 1 candidate gene 1 protein

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. An homologous protein in rat has been shown to function in neuronal migration in the developing neocortex. 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. Alternative splicing results in multiple transcript variants. Read-through transcription also exists between this gene and the downstream cell cycle progression 1 (CCPG1) gene. [provided by RefSeq, Mar 2011]
Research Area Controls and Markers antibody; Neuroscience antibody
Calculated MW 49 kDa