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Invitrogen™ FAM3D Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5109708
Description
Immunogen sequence: RSYMSFSMKT IRLPRWLAAS PTKEIQVKKY KCGLIKPCPA NYFAFKICSG AANVVGPTMC FEDRMIMSPV KNNVGRGLNI ALVNGTTGAV LGQKAFDMYS GDVMHLVKFL KEIPGGALVL VASYDDPGTK MNDESRKLFS DLGSSYAKQL GFRDSWVFIG AKDLRGKSPF EQFLKNSPDT N.
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
FAM3D | |
Polyclonal | |
Unconjugated | |
Oit1 | |
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 | |
Rabbit | |
Affinity chromatography | |
RUO | |
18300, 289949 | |
-20°C, Avoid Freeze/Thaw Cycles | |
Liquid |
ELISA, Western Blot | |
2.29 mg/mL | |
PBS with 50% glycerol and 0.01% thimerosal; pH 7.3 | |
P97805 | |
Fam3d, Oit1 | |
Recombinant fusion protein containing a sequence corresponding to amino acids 24-204 of human FAM3D (NP_620160.1). | |
100 μL | |
Primary | |
Mouse, Rat | |
Antibody | |
IgG |
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