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The antibody against COG7 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 511-770 of human COG7 (NP_705831.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on IF/ICC, ELISA.
The antibody against COG7 was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 511-770 of human COG7 (NP_705831.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on IF/ICC, ELISA.
Immunofluorescence analysis of U2OS cells using COG7 antibody at dilution of 1:100 (40x lens). Blue: DAPI for nuclear staining.
| Cat.No | ADA-06810A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | COG7 |
| Target Synonyms | CDG2E; COG7 | Form | Liquid |
| Species Reactivity | Human | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. | Purification Method | Affinity purification |
| Application | ELISA, IF/ICC |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 511-770 of human COG7 (NP_705831.1). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | P83436 | Immunogen Sequence |
Uniprot Id
P83436
Target Species
Human
Target Name
COG7
Target Full Name
Conserved oligomeric Golgi complex subunit 7
Target Function
Required for normal Golgi function.
Target Involvement
Congenital disorder of glycosylation 2E (CDG2E)
Target Subcellular Location
Golgi apparatus membrane; Peripheral membrane protein.
Target Protein Families
COG7 family
Target Synonyms
CDG2E; COG complex subunit 7; cog7; COG7_HUMAN; Component of oligomeric Golgi complex 7; Conserved oligomeric Golgi complex component 7; Conserved oligomeric Golgi complex subunit 7
Target 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.
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