ARG64674

anti-CDH23 / USH1D antibody

anti-CDH23 / USH1D antibody for Western blot and Human

Neuroscience antibody; Signaling Transduction antibody

Overview

Product Description Goat Polyclonal antibody recognizes CDH23 / USH1D
Tested Reactivity Hu
Tested Application WB
Specificity This antibody is expected to recognize both reported isoforms (NP_071407.3; NP_443068.1).
Host Goat
Clonality Polyclonal
Isotype IgG
Target Name CDH23 / USH1D
Antigen Species Human
Immunogen C-YNISLYENVTVGTS
Conjugation Un-conjugated
Alternate Names CDHR23; Otocadherin; USH1D; Cadherin-23

Application Instructions

Application Suggestion
Tested Application Dilution
WB1 - 3 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: 64072 Human CDH23

Swiss-port # Q9H251 Human Cadherin-23

Background This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Alternative splice variants encoding different isoforms have been described. [provided by RefSeq, Jan 2010]
Research Area Neuroscience antibody; Signaling Transduction antibody
Calculated MW 369 kDa