![COG8 antibody [N3C3]](https://www.genetex.com/upload/website/prouct_img/normal/GTX110375/GTX110375_40464_IFA_w_23060500_307.webp)
![COG8 antibody [N3C3]](https://www.genetex.com/upload/website/prouct_img/normal/GTX110375/GTX110375_40464_WB_w_23060500_215.webp)
GTX110375
COG8 antibody [N3C3]
Cannot supply to this region.
- SKU:
- GTX110375
- Additional Names:
- component of oligomeric golgi complex 8 , CDG2H , DOR1
- Application:
- WB, IF, ICC
- Concentration:
- 1 mg/ml
- Physical State:
- Liquid
- Species Reactivity:
- Human
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
- Supplier:
- Genetex
- Host:
- Rabbit
- Reactivities:
- Human
- Buffer:
- PBS, 1% BSA, 20% Glycerol, 0.01% Thimerosal.
- Immunogen:
- Recombinant protein encompassing a sequence within the center region of human COG8. The exact sequence is proprietary.
- Clone:
- N3C3
- Uniprot:
- Q96MW5
- Synonyms:
- CDG2H;COG complex subunit 8;Component of oligomeric Golgi complex 8;conserved oligomeric golgi complex component 8;conserved oligomeric Golgi complex subunit 8;dependent on RIC1;DOR1
- Extra Details:
- 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. [provided by RefSeq]
- Shipping Conditions:
- Blue Ice