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Invitrogen™ COG8 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA559556
Description
Immunogen sequence: AFANYKTFIR GAECTERIHR LFGDVEASLG RLLDRLPSFQ QSCRNFVKEA EEISSNRRMN SLTLNRHTEI LEILEIPQLM D Highest antigen sequence identity to the following orthologs: Mouse - 96%, Rat - 98%.
This gene 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.
Specifications
COG8 | |
Polyclonal | |
Unconjugated | |
COG8 | |
BB235941; C87832; CDG2H; COG complex subunit 8; Cog8; Component of oligomeric Golgi complex 8; conserved oligomeric golgi complex component 8; conserved oligomeric Golgi complex protein 8; conserved oligomeric Golgi complex subunit 8; dependent on RIC1; DOR1; MNCb-5704 | |
Rabbit | |
Antigen affinity chromatography | |
RUO | |
84342 | |
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles. | |
Liquid |
Immunohistochemistry (Paraffin) | |
0.2 mg/mL | |
PBS with 40% glycerol and 0.02% sodium azide; pH 7.2 | |
Q96MW5 | |
COG8 | |
Recombinant protein corresponding to Human COG8. Recombinant protein control fragment (Product #RP-98595). | |
100 μL | |
Primary | |
Human | |
Antibody | |
IgG |
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