COG2 Antibody Summary
Immunogen |
COG2 (NP_031383.1, 1 a.a. ~ 738 a.a) full-length human protein.MEKSRMNLPKGPDTLCFDKDEFMKEDFDVDHFVSDCRKRVQLEELRDDLELYYKLLKTAMVELINKDYADFVNLSTNLVGMDKALNQLSVPLGQLREEVLSLRSSVSEGIRAVDERMSKQEDIRKKKMCVLRLIQVIRSVEKIEKILNSQSSKETSALEASSPLLTGQILERIATEFNQLQFHAVQSKGMPLLDKVRPRIAGITAMLQQSLEGLLLEGLQTSDVDIIRHCLRTYATIDKTRDAEALVGQVLVKPY
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Specificity |
Reacts with component of oligomeric golgi complex 2.
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Clonality |
Polyclonal
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Host |
Rabbit
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Gene |
COG2
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Purity |
Protein A purified
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Applications/Dilutions
Dilutions |
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Application Notes |
This antibody is reactive against transfected lysate in western blot, and as a detection antibody in ELISA.
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Reactivity Notes
Human
Packaging, Storage & Formulations
Storage |
Store at -20C. Avoid freeze-thaw cycles.
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Buffer |
PBS (pH 7.4)
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Preservative |
No Preservative
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Purity |
Protein A purified
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Notes
This product is produced by and distributed for Abnova, a company based in Taiwan.
Alternate Names for COG2 Antibody
- component of oligomeric golgi complex 2COG complex subunit 2
- conserved oligomeric Golgi complex protein 2
- conserved oligomeric Golgi complex subunit 2
- LDLCbrefeldin A-sensitive, peripheral Golgi protein
- low density lipoprotein receptor defect C complementing
- Low density lipoprotein receptor defect C-complementing protein
Background
This gene encodes a subunit of the conserved oligomeric Golgi complex that is required for maintaining normal structure and activity of the Golgi complex. The encoded protein specifically interacts with the USO1 vesicle docking protein and may be necessary for normal Golgi ribbon formation and trafficking of Golgi enzymes. Mutations of this gene are associated with abnormal glycosylation within the Golgi apparatus. Alternative splicing results in multiple transcript variants.