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- Tel: 858.663.9055
- Email: info@nsjbio.com
TMEM199 encodes a protein homologous to the yeast V-ATPase assembly factor Vma12 and appears to be involved in Golgi homeostasis. The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) in some human cells. Defects in this gene are a cause of congenital disorder of glycosylation, type IIp. By genomic sequence analysis, the TMEM199 gene is mapped to chromosome 17q11.1.
Optimal dilution of the TMEM199 antibody should be determined by the researcher.
Amino acids E20-H129 from the human protein were used as the immunogen for the TMEM199 antibody.
After reconstitution, the TMEM199 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
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