Protein Molecular Weight Markers
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Filtered Search Results
Unchained Labs UNFILTER 96 30 KDA 50-PACK
NC3367373 UNFILTER 96 30 KDA 50-PACK
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NETZSCH INC KINEXUS PRIME ULTRA PLUS RHOME
NC3385581 KINEXUS PRIME ULTRA PLUS RHOME
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EATON CORP FAZ-NA UL 489 MCB 2P 4A
FAZ-NA UL 489 MCB 2P 4A D CURVE
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Shimadzu Scientific Instruments 20 UL MIRC MIXER WITH RECO DEV
NC3442163 20 UL MIRC MIXER WITH RECO DEV
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Avanti Polar Lipids RAC-16-0 PI/5\P-D5-100UG
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NC3828081 RAC-16-0 PI/5\P-D5-100UG
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Santa Cruz Biotechnology HOMOCITRATE SYNTHSE 31F5 500UL
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NC3839842 HOMOCITRATE SYNTHSE 31F5 500UL
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HAWORKS LLC HYALURONATE BIOTIN MW 5 KDA
NC3885164 HYALURONATE BIOTIN MW 5 KDA
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Quanterix Inc QUANTERIX INC
NC3911760 P-TAU 231 ADVANTAGE PLUS KIT
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Genetex Inc GENETEX INC
NC3943587 AIRE ISOFORMS 1 AND 2 ANTIBOD
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ELEMENTAR AMERICAS INC
NC4018289 QUAD-RING BLACK 7.65 X 1.78 MM
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Thermo Scientific THERMO SCI 3P AIG PARTS & ACCESSORIES
NC4026153 PROTEOME DISCOVERR UPGRD F/PRV
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ABclonal Technology CTRB1 Rabbit pAb
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This gene encodes a serine protease that is a precursor of pancreatic proteolytic enzymes. The preproprotein is synthesized in the pancreas and secreted into the small intestine, where it is activated to form the functional enzyme. The CTRB1 gene is located head-to-head with the related CTRB2 gene. Some human populations have a haplotype with a 16.6 Kb inversion region, swapping portions of intron 1, exon 1, and upstream sequences between CTRB1 and CTRB2. This inversion is linked to differential gene expression and an increased risk of chronic pancreatitis. The GRCh38 assembly represents the minor allele for SNP rs8048956 in CTRB1. SNP rs8048956 in intron 1 of CTRB2 is diagnostic for the inversion. The CTRB1 gene encodes distinct isoforms, which may undergo similar processing to generate the mature protein.
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ABclonal Technology RPRD1B Rabbit pAb
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Enables RNA polymerase II complex binding activity and identical protein binding activity. Involved in positive regulation of cell population proliferation, regulation of cell cycle process, and regulation of transcription by RNA polymerase II. Located in nucleoplasm. Part of RNA polymerase II, holoenzyme.
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ABclonal Technology ALDH3A2 Rabbit pAb
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Aldehyde dehydrogenase isozymes are thought to play a major role in the detoxification of aldehydes generated by alcohol metabolism and lipid peroxidation. This gene product catalyzes the oxidation of long-chain aliphatic aldehydes to fatty acid. Mutations in the gene cause Sjogren-Larsson syndrome. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
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ABclonal Technology IQGAP2 Rabbit pAb
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This gene encodes a member of the IQGAP family. The encoded protein contains three IQ domains, one calponin homology domain, one Ras-GAP domain and one WW domain. This protein interacts with components of the cytoskeleton, with cell adhesion molecules, and with several signaling molecules to regulate cell morphology and motility. It also acts as a tumor suppressor and has been found to play a role in regulating innate antiviral responses. Alternative splicing results in multiple transcript variants.
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