Molecular Biology Reagents and Kits
Kd Medical Inc SODIUM CHLORIDE 5M
Reagent used in most common Molecular Biology applications. One 1 Liter bottle.
Sigma Aldrich Fine Chemicals Biosciences GenEluteTM Bacterial Genom
The GenElute Bacterial Genomic DNA kit provides a simple and convenient way to isolate pure genomic DNA from gram-negative bacteria. for most gram-positive bacteria the kit must be used in conjunction with the optional lysozyme (L4919) to effectively lyse the thick peptidoglycan cell walls. A Gram-Positive Lysis SOLUTIONon is provided as a diluent for preparing the lysozyme stock SOLUTIONons.The kit combines the advantages of a silica-based system with a microspin format and eliminates the need for expensive resins alcohol precipitation and hazardous organic compounds such as phenol and chloroform.
Supply Solutions Sigma Aldrich - Isopropyl-b-D-thiogalactoside (IPTG), 5g * Third Party Item
Sigma Aldrich - Isopropyl-b-D-thiogalactoside (IPTG), 5g * Third Party Item
Supply Solutions Sigma Aldrich - Pefabloc SC, 500 mg * Third Party Item
Sigma Aldrich - Pefabloc SC, 500 mg * Third Party Item
Sigma Aldrich Fine Chemicals Biosciences DNase I Amplification Grad
Deoxyribonuclease I (DNase I) is an endonucleaseisolatedfrom bovine pancreas that digests double and single stranded DNA into oligo and mononucleotides. Amplification Grade DNase I has been purified to remove RNase activity and is suitable for eliminating DNA from RNA preparations prior to sensitive applications such as RT-PCR (Reverse Transcriptase - Polymerase Chain Reaction). DNase I digests double- and single-stranded DNA into oligo- and mononucleotides. Using the Reaction Buffer provided DNA is removed from RNA preparations in a 15 minute digestion at room temperature. The DNase I is then inactivated by heating with the Stop SOLUTIONon. Heating also denatures hairpins in the RNA so the RNA can be used directly in reverse transcription.No current RNA isolation procedure removes 100% of the DNA. Many commercial DNase I formulations are contaminated with residual RNases. This RNase contamination can destroy or degrade valuable RNA samples prior to reverse transcription. Laborator
System Biosciences LLC PLL-EF1A-LUCIFERASE LENTIVECTRpLL-EF1a-Luciferase-T2A-Puro (Lenti-Labeler™ plasmid) = 10ug
pLL-EF1a-Luciferase-T2A-Puro Lenti-Labeler™ Lentivector Plasmid & Pre-packaged Virus. SBI’s family of Lenti-Labeler™ constructs facilitate a wide range of studies—including cell tracking, high-throughput assays, and more—by enabling efficient and reliable labeling of your cells. The pLL-EF1α-Luciferase-T2A-Puro Lenti-Labeler™ construct expresses luciferase from the EF1α promoter, which delivers moderate expression in most cell types (including primary and stem cells), and co-expresses the puromycin resistance gene for selection in vitro prior to in vivo use. Available as either fully propagatable, sequence-verified plasmid DNA (Cat.# LL250PA-1) or ready-to-transduce pre-packaged lentivirus (Cat.# LL250VA-1), SBI’s pLL-EF1α-Luciferase-T2A-Puro Lenti-Labeler™ is designed for reliability, so you can get to valuable insights faster.
ABclonal Technology Rubicon Rabbit pAb
The protein encoded by this gene is a negative regulator of autophagy and endocytic trafficking and controls endosome maturation. This protein contains two conserved domains, an N-terminal RUN domain and a C-terminal DUF4206 domain. The RUN domain is involved in Ras-like GTPase signaling, and the DUF4206 domain contains a diacylglycerol (DAG) binding-like motif. Mutation in this gene results in deletion of the DAG binding-like motif and causes a recessive ataxia. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.
