TMEM184B, also known as C22orf5, is a 407 amino acid multi-pass membrane protein and represents a novel gene in the activation of the MAPK signaling pathway. The gene encoding TMEM184B maps to human chromosome 22; mutations in several of the genes in chromosome 22 are involved in the development of autism, schizophrenia, Phelan-McDermid syndrome and Neurofibromatosis type 2, suggesting that TMEM184B may play a role in these syndromes.
140 kDa Ser/Arg-rich domain protein; functional spliceosome-associated protein a; KIAA0332 SR140 U2 associated protein SR140 U2 associated SR140 protein U2SURP; Ser/Arg-rich domain protein, 140 kDa; U2 associated SR140 protein; U2 snRNP-associated SURP domain containing; U2 snRNP-associated SURP motif-containing protein; U2-associated protein SR140; U2-associated SR140 protein
Cat # 16841005
150 µL
Cat # 16851005
20 µL
Cat # 15926950
25µg
Cat # 15715891
100 µL
Cat # 15505162
100 µL
Cat # 15916950
100µg
Cat # 17149003
100 µL
Cat # 16175710
100 uL
Cat # 17128463
100 µL
Cat # 15949094
100 µL
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