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| Product | Description | |
|---|---|---|
| Bsa29 I | One unit of the enzyme is the amount required to hydrolyze 1 μg of Lambda DNA (dam-) in 1 hour at 37°C in a total reaction volume of 50 μl. Applications: After 20-fold overdigestion with enzyme more than 90% of the dna fragments can be ligated and recut. Group: Restriction Enzymes. Purity: 1000U; 5000U. AT↑CGAT TAGC↓TA. Activity: 20000u.a./ml. Appearance: 10 X SE-buffer G, BSA (except E205T and E206T). Storage: -20°C. Form: Liquid. Source: Bacillus stearothermophilus 29. Pack: 10 mM Tris-HCl (pH 7.5); 250 mM NaCl; 0.1 mM EDTA; 7 mM 2-mercaptoethanol; 200 μg/ml BSA; 50% glycerol. Cat No: ET-1041RE. |  |
| BSA for protein quantitation | United States Pharmacopeia (USP) Reference Standard. Group: Pharmacopeia & metrological institutes standards. |  |
| BSA+TMCS | for GC derivatization, 93.0-97.0% (GC). Group: Derivatization reagents gc. | |
| 1, 3, 5(10)-ESTRATRIEN-2, 3, 17β-TRIOL-6-ONE-6-CAROXYMETHYLOXIME:BSA-2-METHYL ETHER | 1, 3, 5(10)-ESTRATRIEN-2, 3, 17β-TRIOL-6-ONE-6-CAROXYMETHYLOXIME:BSA-2-METHYL ETHER. Group: Biochemicals. Alternative Names: 2-METHOXYESTRADIOL-6-CMO:BSA2,3,17β-TRIHYDROXY-1,3,5(10)-ESTRATRIENE-6-ONE-CMO:BSA- 2-METHYL ETHER. US Biological Life Sciences. |  Worldwide |
| 2-Fucosyllactose-APD-BSA | 2-Fucosyllactose-APD-BSA is a vital compound in the biomedical industry utilized for drug development. It serving as a valuable tool for studying deciphering glycan recognition processes associated with fucosylated oligosaccharides. This compound aids in investigating therapeutic interventions for reserching diseases like cancer, inflammatory disorders, and viral infections involving fucosylation. Synonyms: Fuc-a-1,2-Gal-b-1,4-Glc-APD-BSA. |  |
| 2-Fucosyllactose-BSA | | |
| 2'Fucosyllactose-BSA(2'FL-BSA) (3 atom spacer) | 2'Fucosyllactose-BSA(2'FL-BSA) (3 atom spacer) is an unrivaled and invaluable instrument utilized in the biomedical discipline to scrutinize and gain comprehension of the association between fucosylated glycans and precise proteins, for instance, pathogen-binding proteins. Its utilization in the research of maladies entailing said connections, for instance, Hepatitis C and HIV, is widely adopted within the scientific community. | |
| 3a,4b-Galactotriose-BSA | 3a,4b-Galactotriose-BSA is a compound used in the reserch of disorders related to galactose metabolism. It consists of the compound 3a,4b-galactotriose conjugated to bovine serum albumin (BSA), allowing for targeted delivery. Synonyms: α1-3,β1-4 Galactotriose-BSA (3 atom spacer). | |
| 3-Carboxyumbelliferyl b-D-galactoside BSA conjugate | | |
| 3-Fucosyllactose-BSA | | |
| 3-Sialyl-3-fucosyllactose-BSA | | |
| 3-Sialyllactose-BSA | 3-Sialyllactose-BSA is a remarkable compound, serving as an invaluable implement to unravel the intricate association between sialylation and afflictions, encompassing malignant tumors, neurodegenerative conditions and contagious maladies. Synonyms: Neu5Ac-a-2-3-Gal-b-1-4-Glc-spacer BSA. Mole weight: 75595.6. | |
| 3-Sialyl Lewisx-BSA | | |
| 3-Sialyl-N-acetyllactosamine-BSA | 3-Sialyl-N-acetyllactosamine-BSA is an advanced compound, holding promise for combatting glycosylation disorders. It exhibiting exceptional potential as a therapeutic agent, boasting multifaceted benefits such as optimal cellular adhesion, bolstered immune responses is and precise targeted drug delivery. By harnessing the potency of its sialylated glycan structure, this compound revolutionizes receptor recognition and binding, presenting a groundbreaking avenue for pioneering biomedical strategies. With its unparalleled attributes, 3-Sialyl-N-acetyllactosamine-BSA spearheads the frontier of biomedical innovation. Synonyms: 3-Sialyl-N-acetyllactosamine-BSA. | |
| 3-Sulpho Lewisa-BSA | | |
| 3'-Sulpho Lewisa-BSA (3 atom spacer) | 3'-Sulpho Lewisa-BSA (3 atom spacer) is a uniquely crafted protein conjugate that is tailored for the detection of Lewis antigen in cancer cells. With its proprietary binding mechanism that homes in on the glycosyltransferase enzyme, this protein effectively paves the way for accurate measurement of the Lewis antigen levels. Distinguishing this protein from its counterparts in the market, is its 3 atom spacer designed to optimize the protein's affinity to its recognition site, thus magnifying the sensitivity and precision of assays. By exploiting the discovery that the Lewis antigen has been implicated in a spectrum of cancers such as lung, breast, ovarian, and pancreatic, this breakthrough protein holds the potential to serve as a critical diagnostic tool for cancer detection. | |
| 3-Sulpho Lewisx-BSA | | |
| 3'-Sulpho Lewisx-BSA (3 atom spacer) | 3'-Sulpho Lewisx-BSA (3 atom spacer) is a conjugated protein utilized in biomedical research for its exclusive ability to selectively bind to specific glycoproteins. This protein has been highly instrumental in the discovery and characterization of numerous ailments, including inflammatory and cancerous diseases. Its distinct chemical structure, with three sulfur atoms in the spacer region, provides it with an augmented binding affinity to the target molecules. Thus, proving to be a valuable asset in various diagnostic and therapeutic applications. | |
| 4-O-(a-D-Galactopyranosyl)-b-D-galactopyranosyl-CETE-BSA Conjugate | 4-O-(a-D-Galactopyranosyl)-b-D-galactopyranosyl-CETE-BSA Conjugate is a compound standing as an indispensable implement assuming the role of a bespoke transporter to facilitate the intricate dance of targeted drug delivery. Synonyms: Gal-a-1,4-Gal-CETE-BSA Conjugate. Mole weight: 77000. | |
| 6-O-Sulphated Lewisa-BSA | | |
| 6-Sialyllactose-BSA | 6-Sialyllactose-BSA is a compound commonly used in the research of inflammatory diseases and cancers. This compound combines 6-Sialyllactose, a natural glycan, with Bovine Serum Albumin (BSA), making it an effective tool in research of various diseases. Mole weight: 72318. | |
| 6-Sulpho Lewisa-BSA | | |
| 6'-Sulpho Lewisa-BSA (3 atom spacer) | 6'-Sulpho Lewisa-BSA (3 atom spacer) is an extraordinary conjugated protein carrier, with an extremely significant role in the field of biomedical research. Its primary purpose is to detect and target cancer cells expressing the 6'-Sulpho Lewisa antigen, serving as a crucial tool in understanding colon, pancreatic, and ovarian cancers. By employing this innovative carrier in immunoassays and immunohistochemistry, researchers have discovered new ways to unravel the complexities of cancer, uncovering answers to questions that were once believed to be beyond comprehension. | |
| 6-Sulpho Lewisx-BSA | | |
| 6'-Sulpho Lewisx-BSA (3 atom spacer) | 6'-Sulpho Lewisx-BSA (3 atom spacer) is a product used in biomedical research for the detection and analysis of selectin receptors involved in the formation of blood clots and metastasis of cancer cells. This conjugate may also serve as a tool in drug discovery for targeting related diseases and disorders. | |
| a1,2-Mannobiose-BSA | | |
| a1-3,a1-6-Mannotriose-BSA | | |
| a1,3-Mannobiose-BSA | | |
| a1,4-Mannobiose-BSA | | |
| a1,6-Mannobiose-BSA | | |
| Aflatoxin (BSA) | Aflatoxins belong to the class of mycotoxins. Toxic fungal metabolite and carcinogen. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| α1,6-Mannobiose-BSA (3 atom spacer) | α1,6-Mannobiose-BSA (3 atom spacer), a biomolecule of significant value to biomedicine, holds within its structural framework the potential to effectively and specifically bind to specific immune receptors, thus augmenting and activating cell proliferation. Its clinical significance shines through as it has been identified to possess considerable potential towards treating cancer and autoimmune diseases. This biomolecule, coupled with BSA and a spacer molecule, affords stability and specificity, thereby providing a potent ammunition in targeting immune cells with precision. | |
| Amphetamine (BSA) | Amphetamine is a psychostimulant drug of the phenethylamine class that is known to produce increased wakefulness and focus in association with decreased fatigue and appetite. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Amphetamine (BSA) | Labeling Position: Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Anti-Bovine Albumin (BSA)?Agarose antibody produced in rabbit | IgG fraction of antiserum, PBS suspension. Group: Fluorescence/luminescence spectroscopy. | |
| b1-4-Galactosyl-Galactose-BSA | | |
| Barbital (BSA) | Barbiturates are a class of around 12 compounds derivatized from barbituric acid. They are central nervous system (CNS) depressants and can be used as sedatives, hypnotics, anaesthetics and anti-epileptic drugs. Barbiturates can be divided into three main groups according to their duration of action. The ultra-short-acting barbiturates are used clinically as anaesthetics while the long-acting barbiturates have anti-convulsant properties. The short-acting compounds are typically used as hypnotics. The short-acting barbiturates are extensively metabolised by the liver to more pharmacologically inactive hydroxylated compounds. Only a small proportion of parent compound (<0.2%) appears in the urine collected after 24 hours. However, with large doses, there is usually sufficient of the parent compound present to give an adequate response and some of the hydroxylated metabolites will also crossreact in immunoassays. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Barbiturate (BSA) | Barbiturates belong to the group of medicines called central nervous system (CNS) depressants (medicines that cause drowsiness). They affect GABA receptors (like GHB) and thereby bring about a general inhibition of the activity of the CNS, especially that part of the brain stem which governs the rhythm of waking and sleeping. Some of the barbiturates may be used before surgery to relieve anxiety or tension. The only activating stimuli which are not inhibited by barbiturates are pain stimuli. In addition, some of the barbiturates are used as anticonvulsants to help control seizures in certain disorders or diseases, such as epilepsy. Barbiturates have been used to treat insomnia but if they are used regularly (for example, every day) for insomnia, they are usually not effective for longer than 2 weeks. Barbiturates have also been used to relieve nervousness or restlessness during the daytime. Barbiturates have generally been replaced by safer medicines for the treatment of insomnia and d Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Benzodiazepine (BSA) | The term benzodiazepine refers to the portion of the structure composed of a benzene ring fused to a seven membered diazepine ring. Benzodiazepine is a central nervous system depressants, a sedative hypnotic agent. Benzodiazepine receptors are located on the alpha subunit of the GABA receptor located almost exclusively on postsynaptic nerve endings in the CNS (especially cerebral cortex). Benzodiazepines enhance the GABA transmitter in the opening of postsynaptic chloride channels which leads to hyperpolarization of cell membranes. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Benzodiazepine (BZO) (BSA) | The term benzodiazepine refers to the portion of the structure composed of a benzene ring fused to a seven membered diazepine ring. Benzodiazepine is a central nervous system depressants, a sedative hypnotic agent. Benzodiazepine receptors are located on the alpha subunit of the GABA receptor located almost exclusively on postsynaptic nerve endings in the CNS (especially cerebral cortex). Benzodiazepines enhance the GABA transmitter in the opening of postsynaptic chloride channels which leads to hyperpolarization of cell membranes. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Benzodiazepine (Oxazepam) (BSA) | The term benzodiazepine refers to the portion of the structure composed of a benzene ring fused to a seven membered diazepine ring. Benzodiazepine is a central nervous system depressants, a sedative hypnotic agent. Benzodiazepine receptors are located on the alpha subunit of the GABA receptor located almost exclusively on postsynaptic nerve endings in the CNS (especially cerebral cortex). Benzodiazepines enhance the GABA transmitter in the opening of postsynaptic chloride channels which leads to hyperpolarization of cell membranes. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Benzoylecgonine (BSA) (BE, Cocaine) | Benzoylecgonine is the predominant cocaine metabolite. The compound is not biologically active, but is used as an indicator of cocaine use. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Blood group A-BSA (6 atom spacer) | Blood group A-BSA (6 atom spacer), a biomedical diagnostic and therapeutic product, finds application in certain specific blood disorders. Widely used to differentiate and identify A and B blood types, it provides superior accuracy and sensitivity thanks to the 6 atom spacer, which amplifies its clinical value. | |
| Blood Group A trisaccharide-APE,Biotin-BSA | Blood Group A trisaccharide-APE is an essential compound used in compound for the detection and identification of blood group A antigens. It acting as a specific probe for identifying individuals with blood type A and plays a crucial role in blood transfusion compatibility testing and forensic investigations. while Biotin-BSA is a valuable compound extensively utilized in the biomedical industry. It serving as an important tool for numerous applications including immunohistochemistry, ELISA assays is and protein labeling. Biotin-BSA conjugates enable the specific detection and visualization of different biomolecules, proteins, or antibodies in various diagnostic and research settings. Synonyms: GalNAc-a-1,3-(Fuc-a-1,2)Gal-APE-[Biotin]-BSA. | |
| Blood Group A trisaccharide-BSA | Blood Group A trisaccharide-BSA is an Invaluable biomedical research tool unraveling the intricate complexities surrounding blood group antigens and their enigmatic interactions. Adopted prevalently within the biomedical research domain, it is used for the research of A antigen in both blood transfusion reactions and the enigma-laden realm of autoimmune diseases. Synonyms: GalNAc-a-1,3-(Fuc-a-1,2)Gal-BSA. | |
| Blood group B-BSA (6 atom spacer) | Blood group B-BSA (6 atom spacer) is a specialized compound serving as a tool for studying the interaction between blood group B antigens and specific antibodies. This compound aids in investigating blood compatibility, antigen-antibody reactions and the development of diagnostic tests related to blood group B. | |
| Blood group B trisaccharide-APE,Biotin-BSA | Blood Group B Trisaccharide-APE is a specialized compound used for studying intrigue surrounding interactions and recognition processes involving the blood group B antigen. While Biotin-BSA is a remarkable amalgamation of bovine serum albumin (BSA) and biotin. Serving as an invaluable tool, it effectively facilitates detection and visualization of biotinylated molecules in an array of diagnostic and research applications. Moreover, it assumes a pivotal role in the refinement of assays, immunoassays, and bioconjugation techniques. Synonyms: Gal-a-1,3(Fuc-a-1,2)Gal-APE-[Biotin]-BSA. | |
| Blood Group B Trisaccharide-BSA | | |
| Blood Group B Trisaccharide-BSA (20 atom spacer) | Blood Group B Trisaccharide-BSA (20 atom spacer) - an indispensable asset to the biomedicine industry, serves as a valuable tool in the quest to understand how blood type affects the immune system. Through studying the role of ABO blood group antigens in debilitating diseases such as cancer, infection, and autoimmune disorders, this compound uniquely offers a glimpse into the complex biological mechanisms that underlie these conditions. Its manifold uses render it an invaluable asset, contributing significantly to the advancement of biomedical research. | |
| Blood Group B Trisaccharide-BSA (3 atom spacer) | Blood Group B Trisaccharide-BSA (3 atom spacer), a biomedical product of immense importance, plays a crucial role in the detection of the B antigen in individuals. By identifying the presence of this antigen in blood samples, it aids in determining the patient's blood type, enabling effective healthcare provisions. Its application extends beyond diagnostics, and it is widely used in cutting-edge research studies to investigate complex interplays between blood group antigens, antibodies, and pathogens such as bacteria and viruses. With its unparalleled capabilities, there is no doubt that this product is indispensable in the scientific community. | |
| Blood Group H-BSA | | |
| Blood Group H-BSA (15 atom spacer) | Blood Group H-BSA (15 atom spacer) is an indispensable biomolecular tool that plays an important role in biomedicine by enabling improved detection and rigorous analysis of blood group antigens, which are fundamental to understanding human immune function. Utilizing this product in experimental settings provides valuable insights into the molecular recognition of H blood group antigens by chaperone and polymerase proteins, with potential applications in cancer diagnosis and treatment. | |
| Blood group H disaccharide-BSA | | |
| Blood group H disaccharide-BSA (3 atom spacer) | Blood group H disaccharide-BSA (3 atom spacer) is an exceedingly efficacious substrate that is widely utilized within the biomedical arena for promoting intensive analysis and experimentation towards finding life-saving remedies for diverse blood group-related ailments. Impressed with the intricate design of this product, researchers are able to tactfully target and engage with the H antigen decidedly expressed on red blood cells, which play a crucial role in an array of transfusion reactions. It is clinically proven that infectious diseases, autoimmune hemolytic anemia, and cancer are amongst those that this incisive product plays an instrumental role in treating. The property of its unconventional make-up further allows it to be employed across a vast array of applications, including antibody production, glycobiology research, and diagnostic assays. | |
| b-Trisaccharide-APE-Biotin-BSA | | |
| Buprenorphine (BSA) | Buprenorphine (or colloquially, "Bupe") is a semi-synthetic opiate with partial agonist and antagonist actions. Buprenorphine hydrochloride was first marketed in the 1980s by Reckitt & Colman (now Reckitt Benckiser) as an analgesic, available generally as Temgesic 0.2mg sublingual tablets, and as Buprenex in a 0.3mg/ml injectable formulation. In October 2002, the Food and Drug Administration (FDA) of the United States of America additionally approved Suboxone and Subutex, buprenorphine's high-dose sublingual pill preparations for opioid addiction, and as such the drug is now also used for this purpose. In the USA, it has been a Schedule III drug under the United Nations' Convention on Psychotropic Substances since it was rescheduled from Schedule V (the schedule with the lowest restrictions and penalties in the USA) just before FDA approval of Suboxone and Subutex. In the recent years, buprenorphine has been introduced in most European countries as a transdermal formulation ("patch") f Group: Biochemicals. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Buprenorphine (BUP) (BSA) | Buprenorphine (or colloquially, "Bupe") is a semi-synthetic opiate with partial agonist and antagonist actions. Buprenorphine hydrochloride was first marketed in the 1980s by Reckitt & Colman (now Reckitt Benckiser) as an analgesic, available generally as Temgesic 0.2 mg sublingual tablets, and as Buprenex in a 0.3 mg/ml injectable formulation. In October 2002, the Food and Drug Administration (FDA) of the United States of America additionally approved Suboxone and Subutex, buprenorphine's high-dose sublingual pill preparations for opioid addiction, and as such the drug is now also used for this purpose. In the USA, it has been a Schedule III drug under the United Nations' Convention on Psychotropic Substances[1] since it was rescheduled from Schedule V (the schedule with the lowest restrictions and penalties in the USA) just before FDA approval of Suboxone and Subutex. In the recent years, buprenorphine has been introduced in most European countries as a transdermal formulation ("patc Group: Biochemicals. Grades: Purified. Pack Sizes: 500ug. US Biological Life Sciences. | Worldwide |
| Custom Protein Conjugation, BSA | Custom Protein Conjugation, BSA. Group: Molecular Biology. US Biological Life Sciences. | Worldwide |
| Cysteine, S-Nitrosylated (SNO-Cys) (BSA) | Nitric oxide (NO), generated by cell type-specific NO- synthase (NOS) isoforms, is a freely diffusible intercellular messenger that functions in target cells in NOS-dependent signaling. S-nitrosylation of cysteine thiols in proteins by the highly labile NO radical has been identified as an important effector of NO-related bioactivity both in NOS- containing cells and intercellular signaling. Most cells contain low levels of nitrosylated proteins that are thought to be regulated by S-nitrosylation and denitrosylation. S-nitrosylation of proteins serves as a ubiquitous post- translational modification that dynamically regulates a broad functional spectrum of proteins. The majority of these proteins are regulated by S-nitrosylation on a single critical cysteine residue within an acidic/basic or hydrophobic structural motif that may also be subject to oxygen- or glutathione-dependent modification. NO- sensitive ion channels including the cardiac and skeletal muscle ryanodine receptor (RyR1 Group: Biochemicals. Grades: Purified. Pack Sizes: 100ug. US Biological Life Sciences. | Worldwide |
| D-Galactose-BSA | | |
| D-Glucose-BSA | | |
| Digoxin (BSA) | Digoxin is a drug originally derived from the foxglove plant, Digitalis lanata. Digoxin is used primarily to improve the pumping ability of the heart in congestive heart failure (CHF). It is also used to help normalize some dysrhythmias (abnormal types of heartbeat). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Di-Lex-APE-BSA | Di-Lex-APE-BSA is a highly potent analysis tool combining Di-Lex-APE with Bovine Serum Albumin (BSA), enabling effective detection and analysis of various drug interactions and disease markers. The Di-Lex-APE-BSA is extensively utilized in research laboratories and clinical settings for studying drug-target interactions. Synonyms: Galb1-4(Fuca1-3)GlcNAcb1-3Galb1-4(Fuca1-3)GlcNAcb1-O-APE-BSA. | |
| D-Mannose-BSA | | |
| D-Xylose-BSA | | |
| EDDP (2-Ethylidene-1, 5-Dimethyl-3, 3-Diphenylpyrrolidine) (BSA) | Methadone maintenance treatment is a widely used therapy in the rehabilitation of opioid addiction the world over. Methadone is metabolised in the body to a number of inactive metabolites, but primarily to 2-ethylidene-1,5-dimethyl-3,3-diphenylpyrrolidine (EDDP). Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Gala1-2Gal-BSA | | |
| GalNAc-BSA | | |
| Gentamycin (Gentamicin) (BSA) | Precursor: Gentamycin Sulfate. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| Globo-H BSA conjugate | |
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