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Positive test controls include: A-549, BT-474, HL-60, Mouse liver, Mouse kidney, Mouse heart, Rat brain. The target is usually found in the following locations: Membrane, Single-pass membrane protein.
Immunogen sequence: MEGGGGIPLE TLKEESQSRH VLPASFEVNS LQKSNWGFLL TGLVGGTLVA VYAVATPFVT PALRKVCLPF VPATTKQIEN VVKMLRCRRG SLVDIGSGDG RIVIAAAKKG FTAVGYELNP WLVWYSRYRA WREGVHGSAK FYISDLWKVT FSQYSNVVIF GVPQMMLQLE KKLERELEDD ARVIACRFPF PHWTPDHVTG EGIDTVWAYD ASTFRGREKR PCTSMHFQLP IQA
FAM173B is a 233 amino acid single-pass membrane protein that is encoded by a gene that maps to human chromosome 5, which makes up about 6% of human genomic DNA and contains 181 million base pairs encoding around 1,000 genes. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: ATP synthase subunit C lysine N-methyltransferase; family with sequence similarity 173, member B; hFAM173B; mFam173b; protein FAM173B; Protein N-lysine methyltransferase FAM173B
基因别名: A930016P21Rik; AA987072; ATPSCKMT; FAM173B; JS-2; RGD1560629
UniProt ID: (Human) Q6P4H8, (Mouse) Q9D1Z3, (Rat) D3ZLY0
Entrez Gene ID: (Human) 134145, (Mouse) 68073, (Rat) 499561