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COG8 blocking peptide

COG8 Immunizing Peptide

Gene Names
COG8; DOR1; CDG2H
Reactivity
Human
Synonyms
COG8; COG8 Immunizing Peptide; component of oligomeric golgi complex 8; DOR1; FLJ22315; conserved oligomeric golgi complex component 8; dependent on RIC1; COG8 blocking peptide
Ordering
For Research Use Only!
Reactivity
Human
Form/Format
100ug of dried peptide
Sequence
C-KAIQETVEKFQEE
Sequence Length
612
Preparation and Storage
Shipped at ambient temperature, store at -20 degree C

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
Molecular Weight
68,424 Da
NCBI Official Full Name
conserved oligomeric Golgi complex subunit 8
NCBI Official Synonym Full Names
component of oligomeric golgi complex 8
NCBI Official Symbol
COG8
NCBI Official Synonym Symbols
DOR1; CDG2H
NCBI Protein Information
conserved oligomeric Golgi complex subunit 8
UniProt Protein Name
Conserved oligomeric Golgi complex subunit 8
UniProt Gene Name
COG8
UniProt Synonym Gene Names
COG complex subunit 8
UniProt Entry Name
COG8_HUMAN

NCBI Description

This gene encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq, Jul 2008]

Uniprot Description

COG8: Required for normal Golgi function. Defects in COG8 are the cause of congenital disorder of glycosylation type 2H (CDG2H). CDGs are a family of severe inherited diseases caused by a defect in protein N- glycosylation. They are characterized by under-glycosylated serum proteins. These multisystem disorders present with a wide variety of clinical features, such as disorders of the nervous system development, psychomotor retardation, dysmorphic features, hypotonia, coagulation disorders, and immunodeficiency. The broad spectrum of features reflects the critical role of N-glycoproteins during embryonic development, differentiation, and maintenance of cell functions. Belongs to the COG8 family.

Protein type: Vesicle

Chromosomal Location of Human Ortholog: 16q22.1

Cellular Component: Golgi membrane; Golgi transport complex; membrane; trans-Golgi network membrane

Molecular Function: protein binding

Biological Process: ER to Golgi vesicle-mediated transport; intra-Golgi vesicle-mediated transport; protein transport

Disease: Congenital Disorder Of Glycosylation, Type Iih

Research Articles on COG8

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Product Notes

The COG8 cog8 (Catalog #AAA426922) is a Blocking Peptide and is intended for research purposes only. The product is available for immediate purchase. The COG8 Immunizing Peptide reacts with Human and may cross-react with other species as described in the data sheet. The amino acid sequence is listed below: C-KAIQETVE KFQEE. It is sometimes possible for the material contained within the vial of "COG8, Blocking Peptide" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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