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NSJ Bioreagents

SKU:RQ8196

CEP164 Antibody / Centrosomal protein of 164 kDa

CEP164 Antibody / Centrosomal protein of 164 kDa

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Centrosomal protein of 164 kDa, also known as CEP164, is a protein that in humans is encoded by the CEP164 gene. This gene encodes a centrosomal protein involved in microtubule organization, DNA damage response, and chromosome segregation. The encoded protein is required for assembly of primary cilia and localizes to mature centrioles. Defects in this gene are a cause of nephronophthisis-related ciliopathies. Two transcript variants encoding different isoforms have been found for this gene.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Human
Application WB, IF, FACS, Direct ELISA
Application Details Western blot: 0.5-1ug/ml,Immunofluorescence: 5ug/ml,Flow cytometry: 1-3ug/million cells,Direct ELISA: 0.1-0.5ug/ml
Application Note Optimal dilution of the CEP164 antibody should be determined by the researcher.
Localization Cytoplasmic, nuclear
Immunogen E. coli-derived recombinant human protein (amino acids D10-R903) was used as the immunogen for the CEP164 antibody.
Buffer Lyophilized from 1X PBS with 2% Trehalose
Purity Antigen affinity purified
Storage After reconstitution, the CEP164 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Limitation This CEP164 antibody is available for research use only.
Uniprot # Q9UPV0
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/cep164-antibody-centrosomal-protein-of-164-kda-rq8196
Title CEP164 Antibody / Centrosomal protein of 164 kDa
Description Centrosomal protein of 164 kDa, also known as CEP164, is a protein that in humans is encoded by the CEP164 gene. This gene encodes a centrosomal protein involved in microtubule organization, DNA damage response, and chromosome segregation. The encoded protein is required for assembly of primary cilia and localizes to mature centrioles. Defects in this gene are a cause of nephronophthisis-related ciliopathies. Two transcript variants encoding different isoforms have been found for this gene.
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