COG8 antibody
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- Target See all COG8 Antibodies
- COG8 (Component of Oligomeric Golgi Complex 8 (COG8))
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Reactivity
- Human
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This COG8 antibody is un-conjugated
- Application
- Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)
- Cross-Reactivity
- Human
- Purification
- Purified by antigen-affinity chromatography.
- Immunogen
- Recombinant protein encompassing a sequence within the center region of human COG8. The exact sequence is proprietary.
- Isotype
- IgG
- Top Product
- Discover our top product COG8 Primary Antibody
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- Application Notes
- WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- Comment
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Positive Control: Raji
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 mg/mL
- Buffer
- 1XPBS ( pH 7), 1 % BSA, 20 % Glycerol, 0.01 % Thimerosal
- Preservative
- Thimerosal (Merthiolate)
- Precaution of Use
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- 4 °C,-20 °C
- Storage Comment
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Target
- COG8 (Component of Oligomeric Golgi Complex 8 (COG8))
- Alternative Name
- component of oligomeric golgi complex 8 (COG8 Products)
- Synonyms
- CDG2H antibody, DOR1 antibody, BB235941 antibody, C87832 antibody, component of oligomeric golgi complex 8 antibody, Cog8 antibody, cog8 antibody, COG8 antibody
- Background
- Component of oligomeric golgi complex 8 , CDG2H , DOR1,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]
- Molecular Weight
- 68 kDa
- Gene ID
- 84342
- UniProt
- Q96MW5
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