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ABN1365Osteopetrosis-associated transmembrane protein 1 (UniProt: Q86WC4 also known as Chloride channel 7 beta subunit) is encoded by the OSTM1 (also known as GL) gene (Gene ID: 28962) in human. Osteopetrosis-associated transmembrane protein 1 is a
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ABN1362RNA-binding protein with multiple splicing (UniProt Q93062 also known as Heart and RRM expressed sequence, Hermes, RBP-MS) is encoded by the RBPMS (also known as HERMES) gene (Gene ID 11030) in human. RBPMS is a member of the RRM (RNA recognition
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ABN1361Expansion of a GGGGCC (G4C2) hexanucleotide repeat sequence in the non-coding region of human chromosome 9 open reading frame 72 or C9orf72 (also known as ALSFTD, FTDALS Gene ID 203228) is the most common genetic abnormality in familial and
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ABN1360
Sigma-Aldrich
Anti-C9ORF72 (alpha-GR sense Antibody, CT) (C15-1317-340)
Price: $759.43List Price: $843.81Expansion of a GGGGCC (G4C2) hexanucleotide repeat sequence in the non-coding region of human chromosome 9 open reading frame 72 or C9orf72 (also known as ALSFTD, FTDALS Gene ID 203228) is the most common genetic abnormality in familial and -
ABN1358
Sigma-Aldrich
Anti-C9ORF72/C9RANT (Poly-GP sense/antisense) (C15-1317-339)
Price: $785.14List Price: $872.38Expansion of a GGGGCC (G4C2) hexanucleotide repeat sequence in the non-coding region of human chromosome 9 open reading frame 72 or C9orf72 (also known as ALSFTD, FTDALS Gene ID 203228) is the most common genetic abnormality in familial and -
ABN1357Expansion of a GGGGCC (G4C2) hexanucleotide repeat sequence in the non-coding region of human chromosome 9 open reading frame 72 or C9orf72 (also known as ALSFTD, FTDALS Gene ID 203228) is the most common genetic abnormality in familial and
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ABN1356Expansion of a GGGGCC (G4C2) hexanucleotide repeat sequence in the non-coding region of human chromosome 9 open reading frame 72 or C9orf72 (also known as ALSFTD, FTDALS Gene ID 203228) is the most common genetic abnormality in familial and
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ABN1354Expansion of a GGGGCC (G4C2) hexanucleotide repeat sequence in the non-coding region of human chromosome 9 open reading frame 72 or C9orf72 (also known as ALSFTD, FTDALS Gene ID 203228) is the most common genetic abnormality in familial and
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ABN1350
Sigma-Aldrich
Anti-ApoE4 Fragment nApoECF Antibody (Asp172) (C15-1317-335)
Price: $759.43List Price: $843.81Apolipoprotein E (UniProt P02649 also known as Apo-E) is encoded by the APOE (also known as AD2, LDLCQ5, LPG) gene (Gene ID 348) in human. Apolipoprotein E (ApoE) is found in the chylomicron and Intermediate-density lipoprotein (IDLs) and is -
ABN1347-25UL
Sigma-Aldrich
Anti-Glutathione S-transferase A5 (GSTA5) (C15-1317-334)
Price: $323.27List Price: $359.18Glutathione S-transferase A5 (UniProt: Q7RTV2 also known as EC: 2.5. -
ABN1347
Sigma-Aldrich
Anti-Glutathione S-transferase A5 (GSTA5) (C15-1317-333)
Price: $666.86List Price: $740.95Glutathione S-transferase A5 (UniProt: Q7RTV2 also known as EC: 2.5. -
ABN1346Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 1 (EC 3.1.