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COG8 Antibody - BSA Free

Novus Biologicals, part of Bio-Techne | Catalog # NBP3-47564

Novus Biologicals, part of Bio-Techne
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NBP3-47564

Key Product Details

Species Reactivity

Human, Mouse, Rat

Applications

ELISA, Western Blot

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Format

BSA Free

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Product Specifications

Immunogen

component of oligomeric golgi complex 8. (Uniprot# Q96MW5)

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Theoretical MW

68 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Description

Novus Biologicals Rabbit COG8 Antibody - BSA Free (NBP3-47564) is a polyclonal antibody validated for use in WB and ELISA. All Novus Biologicals antibodies are covered by our 100% guarantee.

Scientific Data Images for COG8 Antibody - BSA Free

COG8 Antibody - BSA Free

Western Blot: COG8 Antibody - BSA Free [NBP3-47564] -

Western Blot: COG8 Antibody - BSA Free [NBP3-47564] - HeLa cells were subjected to SDS PAGE followed by western blot with (COG8 antibody) at dilution of 1:400

Applications for COG8 Antibody - BSA Free

Application
Recommended Usage

Western Blot

1:500-1:2000

Formulation, Preparation, and Storage

Purification

Immunogen affinity purified

Formulation

PBS, 50% Glycerol, pH (7.3)

Format

BSA Free

Preservative

0.02% Sodium Azide

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at -20C. Avoid freeze-thaw cycles.

Background: COG8

COG8 encodes a protein that is a component of the conserved oligomeric Golgi (COG) complex, a multiprotein complex that plays a structural role in the Golgi apparatus, and is involved in intracellular membrane trafficking and glycoprotein modification. Mutations in this gene cause congenital disorder of glycosylation, type IIh, a disease that is characterized by under-glycosylated serum proteins, and whose symptoms include severe psychomotor retardation, failure to thrive, seizures, and dairy and wheat product intolerance. [provided by RefSeq]

Alternate Names

COG complex subunit 8, component of oligomeric golgi complex 8CDG2H, conserved oligomeric Golgi complex subunit 8, dependent on RIC1, DOR1conserved oligomeric golgi complex component 8, FLJ22315

Gene Symbol

COG8

Additional COG8 Products

Product Documents for COG8 Antibody - BSA Free

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Product Specific Notices for COG8 Antibody - BSA Free

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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