Anti-COG5 Antibody

$99.00$319.00

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

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Rabbit Anti-COG5 Antibody (CSB-PA890771ESR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Conserved oligomeric Golgi complex subunit 5 Antibody,COG complex subunit 5 Antibody,13S Golgi transport complex 90 kDa subunit Antibody,GTC-90 Antibody,Component of oligomeric Golgi complex 5 Antibody,Golgi transport complex 1 Antibody,COG5 Antibody,GOLTC1 Antibody,GTC90 Antibody

More alternative names for the antibody
13S Golgi transport complex 90 kDa subunit antibody|COG complex subunit 5 antibody|Component of oligomeric Golgi complex 5 antibody|Conserved oligomeric Golgi complex subunit 5 antibody|Golgi transport complex 1 antibody|GOLTC1 antibody|GTC 90 antibody|GTC90 antibody
Anti-COG5 antibody (ab90301)
Close sc-162695|

Recommended applications: ELISA, WB, IHC

Recommended dilution: User optimized

Recommended protocols: check protocols

Name

Anti-COG5 Antibody

Catalogue No.

CSB-PA890771ESR2HU

Reactivity

Human, Mouse

Immunogen

Recombinant human Conserved oligomeric Golgi complex subunit 5 protein (1-260AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

User optimized

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

92 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:10466( Human), Omim:606821( Human), SwissProt:Q9UP83( Human)

Protein function

Required for normal Golgi function. .

Involvement in disease

Congenital disorder of glycosylation 2I (CDG2I) [MIM:613612]: 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. Congenital disorder of glycosylation type 2I is characterized by mild neurological impairments. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the COG5 family.

Protein cellular localization

Cytoplasm, cytosol . 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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