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Rabbit Anti-COG7 Recombinant Antibody (CBWJC-2899) (CBMAB-C4026WJ)

This product is a Rabbit antibody that recognizes COG7. This antibody CBWJC-2899 can be used for immunoassay techniques such as: WB, IHC-P, FC, ICC.
See all COG7 antibodies

Summary

Host Animal
Rabbit
Specificity
Human, Mouse, Rat
Clone
CBWJC-2899
Antibody Isotype
IgG
Application
WB, IHC-P, FC, ICC

Basic Information

Specificity
Human, Mouse, Rat
Antibody Isotype
IgG
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
component of oligomeric golgi complex 7
Introduction
COG7 (Component Of Oligomeric Golgi Complex 7) is a Protein Coding gene. Diseases associated with COG7 include Congenital Disorder Of Glycosylation, Type Ii and Congenital Disorder Of Glycosylation, Type In. Among its related pathways are Transport to the Golgi and subsequent modification and Metabolism of proteins.
Entrez Gene ID
Human91949
Mouse233824
Rat293456
UniProt ID
HumanP83436
MouseQ3UM29
RatQ3T1G7
Alternative Names
Component Of Oligomeric Golgi Complex 7; COG Complex Subunit 7; Conserved Oligomeric Golgi Complex Subunit 7; CDG2E;
Function
Required for normal Golgi function.
Biological Process
Endoplasmic reticulum to Golgi vesicle-mediated transport Source: Reactome
Golgi organization Source: GO_Central
Intracellular protein transport Source: UniProtKB
Protein glycosylation Source: UniProtKB
Protein localization to Golgi apparatus Source: UniProtKB
Protein localization to organelle Source: UniProtKB
Protein stabilization Source: UniProtKB
Retrograde vesicle-mediated transport, Golgi to endoplasmic reticulum Source: UniProtKB
Cellular Location
Golgi apparatus membrane
Involvement in disease
Congenital disorder of glycosylation 2E (CDG2E):
A multisystem disorder caused by a defect in glycoprotein biosynthesis and characterized by under-glycosylated serum glycoproteins. Congenital disorders of glycosylation result in a wide variety of clinical features, such as defects in 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.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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