missing translation for 'onlineSavingsMsg'
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Invitrogen™ FAM3D Monoclonal Antibody (K29027_4E9), Invitrogen™
Description
Sequence of this protein is as follows: YMSFSMKTIR LPRWLAASPT KEIQVKKYKC GLIKPCPANY FAFKICSGAA NVVGPTMCFE DRMIMSPVKN NVGRGLNIAL VNGTTGAVLG QKAFDMYSGD VMHLVKFLKE IPGGALVLVA SYDDPGTKMN DESRKLFSDL GSSYAKQLGF RDSWVFIGAK DLRGKSPFEQ FLKNSPDTNK YEGWPELLEM EGCMPPKPF
FAM3D (FAM3 Metabolism Regulating Signaling Molecule D) is a Protein Coding gene. Diseases associated with FAM3D include Deafness, Autosomal Recessive 17 and Scheuermann Disease. Gene Ontology (GO) annotations related to this gene include cytokine activity. An important paralog of this gene is FAM3C. [GeneCards].
Specifications
Specifications
| Antigen | FAM3D |
| Applications | Western Blot |
| Classification | Monoclonal |
| Clone | K29027_4E9 |
| Concentration | 1 mg/mL |
| Conjugate | Unconjugated |
| Formulation | PBS with 50% glycerol, 0.5% BSA and 0.09% sodium azide |
| Gene | Fam3d |
| Gene Accession No. | Q96BQ1 |
| Gene Alias | 2310076N21Rik; AV067083; cytokine-like protein EF-7; EF7; EF-7; Fam3d; family with sequence similarity 3 member D; family with sequence similarity 3, member D; Oit1; oncoprotein induced transcript 1; oncoprotein induced transcript 1 homolog; oncoprotein-induced protein 1; Protein EF-7; protein FAM3D; UNQ567/PRO1130 |
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