Oligonucleotides
CPC Scientific 5FAM-Ile-Tyr-Ser-Gly-Asp-Tyr-Tyr-Arg-NH2 (trifluoroacetate salt) 0.5MG
SEQUENCE: 5FAM-Ile-Tyr-Ser-Gly-Asp-Tyr-Tyr-Arg-NH2 (trifluoroacetate salt)ONE-LETTER SEQUENCE: 5FAM-IYSGDYYR-NH2MOLECULAR FORMULA: C69H76N12O20MOLECULAR WEIGHT: 1393.4STORAGE CONDITIONS: -20 5 CCAS REGISTRY NUMBER: SYNONYMS: RESEARCH AREA: Protein Kinases and PhosphatasesREFERENCES:SKU(s): PROK-044A, PROK-044B
Perkin Elmer US LLC Diffuse Reflectance Reference Materials Standards - Calibrated, Qty. 8
PerkinElmer's Diffuse Color and Neutral Reference Material sets are used to establish the photometric accuracy and linearity of the LAMBDA 850+ and 1050+ spectrometers. These reference materials are supplied with calibration data from 250 to 2500 nm, reported every 50 nm. Sets also included a disk with data for each 1 nm. Reflectance calibration is traceable to NIST and NPL standards.
ABclonal Technology 14-3-3 zeta/YWHAZ Rabbit mAb
This gene product belongs to the 14-3-3 family of proteins which mediate signal transduction by binding to phosphoserine-containing proteins This highly conserved protein family is found in both plants and mammals and this protein is 99% identical to the mouse rat and sheep orthologs The encoded protein interacts with IRS1 protein suggesting a role in regulating insulin sensitivity Several transcript variants that differ in the 5 UTR but that encode the same protein have been identified for this gene
Medchemexpress LLC Gapdh, rabbit muscle | 9001-50-7 | 73,600 | 500 U
Glyceraldehyde phosphate dehydrogenase (EC 1.2.1.12) is an enzyme that targets anti-thymocyte and anti-apoptotic agents. It catalyzes the chain oxidation of reduced nicotinamide adenine dinucleotide by perhydroxyl radicals. This recombinant product is suitable for enzymatic determination of glycerol and triglycerides when combined with glycerol kinase.
- Solid appearance, white to light yellow
- pH stable between 6.5 and 10.0, with an optimum pH of 9.0
- Soluble in H₂O at concentrations ≥ 25 mg/mL
- For research use only
Medchemexpress LLC CDK7/9 tide | >99.7% | 2690.00 | 10 MG
CDK7/9 tide is a synthetic peptide substrate designed for the study of cyclin-dependent kinases 7 (CDK7) and 9 (CDK9). This research-use-only product is provided as a white to off-white solid and is soluble in water, making it suitable for in vitro applications.
- Sequence shortening: YSPTSPSYSPTSPSYSPTSPSKKKK
- Formula: C120H185N29O41
- Appearance: White to off-white solid
- Solubility: 10 mg/mL in H₂O (requires ultrasonic)
- Storage (powder): -80°C for 2 years, -20°C for 1 year
- Storage (in solvent): -80°C for 6 months, -20°C for 1 month
Eagle Biosciences Inc Hela Cell Residual DNA Detection Kit (qPCR)
Hela Cell Residual DNA Detection Kit (qPCR)
Biolegend Purified anti-HMGA2
Purified anti-HMGA2 [W23012E] Isotype Rat IgG2b Reactivity Human Mouse Rat Apps WB ICC IHC-P Size 100 g
ABclonal Technology CEBPA Rabbit pAb
This intronless gene encodes a transcription factor that contains a basic leucine zipper (bZIP) domain and recognizes the CCAAT motif in the promoters of target genes. The encoded protein functions in homodimers and also heterodimers with CCAAT/enhancer-binding proteins beta and gamma. Activity of this protein can modulate the expression of genes involved in cell cycle regulation as well as in body weight homeostasis. Mutation of this gene is associated with acute myeloid leukemia. The use of alternative in-frame non-AUG (GUG) and AUG start codons results in protein isoforms with different lengths. Differential translation initiation is mediated by an out-of-frame, upstream open reading frame which is located between the GUG and the first AUG start codons.
Cayman Chemical ANTIBODY SET2 10mg
A TRPV2 inhibitor (IC50 = 0.46 µM); selectively inhibits 2-APB-induced currents in a patch-clamp assay using HEK293T cells overexpressing TRPV2 at 0.3 or 1 µM over HEK293T cells overexpressing TRPV1 or TRPV3 at 3 or 10 µM; reduces LPA-induced migration in PC-3M prostate cancer cells at 20 µM; reduces LPA-induced increases in current in a patch-clamp assay using HEK293T cells
BIOHIPPO AAV-VGAT1-WGA-CRE-P2A-EGFP-WPREs
Recombinant adeno associated virus expressing WGA-Cre fused to EGFP under the VGAT1 promoter with WPRE and hGH polyA elements. The Cre dependent configuration enables expression only after recombination, providing precise targeted control of targeted neurons. Offered under the Biohippo AAVX Series with multiple serotypes available including AAV2/1, AAV2/2, AAV2/5, AAV2/6, AAV2/6m, AAV2/6.2FF, AAV2/7m8, AAV2/8, AAV2/9, AAV2/DJ, AAV2/DJ8, AAV2/Retro, AAV2/PHP.eB, AAV2/PHP.B, AAV2/rh10, AAV2/PHP.S, AAV2/anc80, AAV2/B10, AAV2/olig001, AAV2/BI30, AAV2/BR1, AAV2/MG1.2, AAV1/2, AAV2/MaCPNS1, and AAV2/MaCPNS2. Regular titer is greater than or equal to 2.00E+12 vg per mL, with high titer greater than or equal to 1.00E+13 vg per mL available upon request at no additional cost. Customers may specify preferred serotype and titer when placing orders.
Cayman Chemical NotogInsenosIde R1 5mg
A saponin; decreases serum total cholesterol, triacylglycerol, and oxLDL levels, as well as reduces atherosclerotic lesion area and lipid deposition in the aortic root of ApoE-/- mice fed a Western diet at 25 mg/kg per day for 8 weeks; inhibits apoptosis of hippocampal neurons and reduces infarct size in a rat model of cerebral ischemia-reperfusion injury induced by bilateral common carotid artery occlusion at 100 mg/kg; decreases colonic NF-ĸB and MPO activities and TNF-α and IL-6 levels, as well as reduces colonic shortening, tissue damage, and inflammatory cell infiltration in a DSS-induced mouse model of colitis at 25 mg/kg per day for 7 days
ABclonal Technology SLC1A5 Rabbit pAb
The SLC1A5 gene encodes a sodium-dependent neutral amino acid transporter that can act as a receptor for RD114/type D retrovirus (Larriba et al., 2001 [PubMed 11781704]).
ABclonal Technology AFTMag Stool/Soil DNA Extraction Kit (Prepackaged)
This kit is a nucleic acid extraction kit based on magnetic beads. The main principle involves using functional groups on the surface of the magnetic beads to enrich nucleic acids from the sample lysate onto the surface of the beads. The beads are then washed to remove proteins and other impurities. Then, a magnetic separation device is used to isolate the beads, allowing for rapid separation and purification of nucleic acids. The entire process does not require the use of organic reagents such as phenol, chloroform, or β-mercaptoethanol, making it safe and non-toxic. The use of paramagnetic magnetic beads is suitable for high-throughput automated extraction. The extracted product can be directly used for RT-PCR, RT-qPCR, Northern Blot, next-generation sequencing library construction, and cloning.