Cell Line Lysates
Cayman Chemical N6 4AmInobutyladenosIn5 2.5mg
An aminobutyl derivative of ADP; has been used in the synthesis of quantum dots in ADP-specific TR-FRET assays
ABclonal Technology ACSL1 Rabbit pAb
The protein encoded by this gene is an isozyme of the long-chain fatty-acid-coenzyme A ligase family. Although differing in substrate specificity, subcellular localization, and tissue distribution, all isozymes of this family convert free long-chain fatty acids into fatty acyl-CoA esters, and thereby play a key role in lipid biosynthesis and fatty acid degradation. Several transcript variants encoding different isoforms have been found for this gene.
Sino Biological Human HMGB1 / HMG1 Protein (His Tag), Endotoxin-Free 1mg
A DNA sequence encoding the human HMGB1 protein (NP_002119.1) (Met 1-Glu 215) was fused with a polyhistidine tag at the C-terminus and a signal peptide at the N-terminus.
ABclonal Technology ADK Rabbit pAb
This gene an enzyme which catalyzes the transfer of the gamma-phosphate from ATP to adenosine, thereby serving as a regulator of concentrations of both extracellular adenosine and intracellular adenine nucleotides. Adenosine has widespread effects on the cardiovascular, nervous, respiratory, and immune systems and inhibitors of the enzyme could play an important pharmacological role in increasing intravascular adenosine concentrations and acting as anti-inflammatory agents. Multiple transcript variants encoding different isoforms have been found for this gene.
AdipoGen B7-H3 h ELISA Kit
Colorimetric Sandwich ELISA Assay. Detects human B7-H3 CD276 in serum, plasma and cell culture supernatant. Range 0.3125 to 20ng/ml. Sensitivity 0.3ng/ml. Works in Cell Culture Supernatant, Plasma, Serum. B7 family of immunoregulatory proteins is composed of ten members B7-1 CD80, B7-2 CD86, B7-H1 PD-L1, B7-DC PD-L2, B7-H2, B7-H3, B7-H4, B7-H5 VISTA, B7-H6 and B7-H7. B7-H3 or CD276 is a 316aa long type I transmembrane protein. B7-H3 shares 20-27% amino acid identity with other B7 family ligands. Glycosylated B7-H3 protein has a molecular weight of approximately 100 kDa. A B7-H3 soluble isoform has been detected in plasma and B7-H3 is also expressed on exosomes. B7-H3 is ubiquitously expressed by cells in the non-hematopoietic compartment, such as fibroblasts and epithelial cells, it can be induced on T cells and NK cells. Although B7-H3 expression is elevated in tumors, B7-H3 is also constitutively expressed at higher levels in the liver than in other healthy tissue.
Cayman Chemical ANTIBODY USP8-IN-1 5mg
A USP8 inhibitor (IC50 = 2.6 µM); selective for USP8 over USP7 (IC50 = >20 µM); inhibits colony formation by H1975 cells (IC50 = 30.8 µM)
Abcam Human ERMP1 knockout HeLa cell lysate.
Human ERMP1 knockout HeLa cell lysate.
The product is subject to the following: Abcam Restricted Use Statement
Biotium Fibrinogen Alpha Chain(UC45), 0.2mg/mL
The plasma glycoprotein fibrinogen is synthesized in the liver and comprises three structurally different subunits: . Fibrinogen is important in platelet aggregation, the final step of the coagulation cascade (i. e. the formation of fibrin) and determination of plasma viscosity and erythrocyte aggregation. It is both constitutively expressed and inducible during an acute phase reaction. Hemostasis following tissue injury deploys essential plasma procoagulants (prothrombin and factors X, IX, V and VIII), which are involved in a blood coagulation cascade leading to the formation of insoluble fibrin clots and the promotion of platelet aggregation. Following vascular injury, fibrinogen is cleaved by thrombin to form fibrin, which is the most abundant component of blood clots. The cleavage products of fibrinogen regulate cell adhesion and spreading, display vasoconstrictor and chemotactic activities, and are mitogens for several cell types. Primary antibodies are available purifie
Abcam Human VOPP1 knockout HeLa cell lysate.
Human VOPP1 knockout HeLa cell lysate.
The product is subject to the following: Abcam Restricted Use Statement
Sino Biological Recombinant Human SLC30A1 Protein (Nanodisc, His Tag) 500 µg
A DNA sequence encoding the Human SLC30A1(Met1-Leu507) was expressed with a polyhistidine tag at the C-terminus. This protein was prepared using our Nanodisc platform. Nanodisc is a versatile tool for studying membrane proteins. Using styrene-maleic acid (SMA) copolymer, membrane proteins can be extracted directly from prokaryotic and eukaryotic expression systems in the absence of detergents to preserve the protein structure and function better. Compared to membrane scaffold proteins (MSPs) nanodiscs, SMA nanodiscs also have the advantage of preserving proteins' nature by maintaining native lipids surrounded without introducing any heterologous proteins, which allows studies of protein structure and functions in a native-like environment.
Biochain Institute Inc Total Protein - Alzheimer's Disease: Brain: Postcentral Gyrus, 1 mg/PK
Tissue total protein is prepared from whole tissue homogenates. It presents a consistent pattern on SDS-PAGE analysis. The total protein is stored in a buffer with protease inhibitor cocktail, and provided at a concentration of 5 mg/ml.
Innovative Research Inc Hmn NR3C2 Prtn Lysate 20ug
Human NR3C2 Protein Lysate 20ug - Human NR3C2 Protein Lysate 20ug from Innovative Research is provided as a Lyophilized powder. This is a Recombinant Protein Lysate produced in HEK293T cells. This protein lysate can be reconsituted using SDS Sample Buffer. Once reconsituted, aliquot and store any remaining material at -20C to avoid repeated freeze-thaw cycles. Additional Details Species HumanFormat Lyophilized Gene Symbol NR3C2Gene Alias NR3C2, MCR, MLR, MR, NR3C2VIT Protein Accession Number NP_000892 Nucelotide Accession Number NM_000901 Molecular Weight 106.9 kDa Storage Conditions -20C
ABclonal Technology XRCC4 Rabbit pAb
The protein encoded by this gene functions together with DNA ligase IV and the DNA-dependent protein kinase in the repair of DNA double-strand breaks. This protein plays a role in both non-homologous end joining and the completion of V(D)J recombination. Mutations in this gene can cause short stature, microcephaly, and endocrine dysfunction (SSMED). Alternate transcript variants such as NM_022406 are unlikely to be expressed in some individuals due to a polymorphism (rs1805377) in the last splice acceptor site.
ABclonal Technology cIAP1 Rabbit pAb
The protein encoded by this gene is a member of a family of proteins that inhibits apoptosis by binding to tumor necrosis factor receptor-associated factors TRAF1 and TRAF2, probably by interfering with activation of ICE-like proteases. This encoded protein inhibits apoptosis induced by serum deprivation and menadione, a potent inducer of free radicals. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Abcam Human SECTM1 knockout A549 cell lysate.
Human SECTM1 knockout A549 cell lysate.
The product is subject to the following: Abcam Restricted Use Statement