Anti-COG7 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-COG7 Antibody (CSB-PA005711ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

COG complex subunit 7 Antibody,Component of oligomeric Golgi complex 7 Antibody,COG7 Antibody

More alternative names for the antibody
CDG2E antibody|COG complex subunit 7 antibody|cog7 antibody|COG7_HUMAN antibody|Component of oligomeric Golgi complex 7 antibody|Conserved oligomeric Golgi complex component 7 antibody|Conserved oligomeric Golgi complex subunit 7 antibody
Anti-COG7 antibody [EPR9942] (ab168362)
Close sc-271699|sc-101279|

Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-COG7 Antibody

Catalogue No.

CSB-PA005711ESR1HU

Reactivity

Human

Immunogen

Recombinant human Conserved oligomeric Golgi complex subunit 7 protein (511-770AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

86 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:91949( Human), Entrez Gene:233824( Mouse), Entrez Gene:293456( Rat), Omim:606978( Human), SwissProt:P83436( Human), SwissProt:Q3UM29( Mouse), SwissProt:Q3T1G7( Rat), Unigene:185807( Human), Unigene:442015( Mouse), Unigene:23781( Rat)

Protein function

Required for normal Golgi function. .

Involvement in disease

Congenital disorder of glycosylation 2E (CDG2E) [MIM:608779]: 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. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the COG7 family.

Protein cellular localization

Golgi apparatus membrane ; Peripheral membrane protein .

Research area

All research areas>Transport and Trafficking>COG
(View all antibody categories related to Transport and Trafficking)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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