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The antibody against COG7 was raised in rabbit using the Recombinant Human Conserved oligomeric Golgi complex subunit 7 protein (511-770AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
The antibody against COG7 was raised in rabbit using the Recombinant Human Conserved oligomeric Golgi complex subunit 7 protein (511-770AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.
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Immunohistochemistry of paraffin-embedded human cervical cancer using COG7 Antibody at dilution of 1:100
Immunohistochemistry of paraffin-embedded human testis tissue using COG7 Antibody at dilution of 1:1002
| Cat.No | ADC-40415A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | COG7 |
| Form | Liquid | Species Reactivity | Human |
| Isotype | IgG | Storage Buffer | 50% Glycerol, PBS with 0.02% sodium azide, pH7.3. |
| Purification Method | Antigen affinity purified | Conjugate | Non-conjugated |
| Application | ELISA, IHC | Storage | Upon receipt |
| Immunogen Description | Recombinant Human Conserved oligomeric Golgi complex subunit 7 protein (511-770AA) | Target Species | Human |
|---|---|---|---|
| Immunogen Sequence | Complete sequences for the immunogen, target protein, and peptides are available upon request. | Uniprot ID | P83436 |
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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