ELK Biotechnology
COG7 Rabbit Polyclonal Antibody - ES17336
COG7 Rabbit Polyclonal Antibody - ES17336
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COG7 Rabbit Polyclonal Antibody
Sizes: 50μL, 100μL
Catalogue Numbers: ES17336-50, ES17336-100
Lead times: 1-2 weeks, if manufacturer has product in stock
Manufacturer/Ship Location: China
Background: The protein encoded by this gene resides in the golgi, and constitutes one of the 8 subunits of the conserved oligomeric Golgi (COG) complex, which is required for normal golgi morphology and localization. Mutations in this gene are associated with the congenital disorder of glycosylation type IIe.[provided by RefSeq, May 2010],
Reactivity: Human, Mouse, Rat
Host: Rabbit
Applications: WB
Alternate Names: Conserved oligomeric Golgi complex subunit 7 (COG complex subunit 7) (Component of oligomeric Golgi complex 7)
Clonality: Polyclonal
Immunogen: Synthesized peptide derived from human COG7 AA range: 245-295
Isotype: IgG
Target: COG7
Specificity: This antibody detects endogenous levels of COG7 at Human/Mouse/Rat
Dilution: WB 1:500-2000
Purification: The antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.
Concentration: 1 mg/ml,
Formlation: Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.332% sodium azide.
Expression: Brain, Mammary gland, Synovial membrane,
Observed Band (KD): 85kD
Function: Disease: Defects in COG7 are the cause of congenital disorder of glycosylation type 2E (CDG2E) [MIM: 608779]. 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
Function: Required for normal Golgi function
Similarity: Belongs to the COG7 family
Subunit: Component of the conserved oligomeric Golgi complex which is composed of eight different subunits and is required for normal Golgi morphology and localiz
Subcellular Location: Golgi apparatus membrane, Peripheral membrane protein
Storage and Stability: -20°C/1 year
Gene Name: COG7 UNQ3082/PRO10013
Protein Name: COG7
Mouse Gene ID: 233824
Mouse SwissProt Number: Q3UM29
Rat Gene ID: 293456
Rat SwissProt Number: Q3T1G7
Research Use Only
