• Target：
• TM199

• Gene Name：
• TMEM199 C17orf32

• Protein Name：
• TM199

• Human Gene Id：
• 147007

• Human Swiss Prot No：
• Q8N511

• Mouse Gene Id：
• 195040

• Mouse Swiss Prot No：
• Q5SYH2

• Rat Gene Id：
• 303332

• Rat Swiss Prot No：
• Q5BK13

• Immunogen：
• Synthesized peptide derived from human TM199 AA range: 38-88

• Specificity：
• This antibody detects endogenous levels of TM199 at Human/Mouse/Rat

• Formulation：
• Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.

• Source：
• Polyclonal, Rabbit,IgG

• Dilution：
• WB 1：500-2000

• Purification：
• The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

• Concentration：
• 1 mg/ml

• Storage Stability：
• -15°C to -25°C/1 year(Do not lower than -25°C)

• Molecular Weight(Da)：
• 23kD

• Background：
• 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. The encoded protein shares some homology with the yeast protein Vma12. Defects in this gene are a cause of congenital disorder of glycosylation, type IIp. [provided by RefSeq, Mar 2016],

• Subcellular Location：
• Cytoplasmic vesicle, COPI-coated vesicle membrane ; Multi-pass membrane protein . Endoplasmic reticulum-Golgi intermediate compartment membrane ; Multi-pass membrane protein . Endoplasmic reticulum membrane ; Multi-pass membrane protein . Partial colocalization with GOLGB1. .

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