| Description | Clindamycin hydrochloride (neutralizer) is a water-soluble protein using a recombinant gene and is a dark brown liquid. A recombinant gene protein based on the chemical structure of clindamycin hydrochloride. The active center of its gene fragment can destroy the chemical structure formula of Clindamycin hydrochloride (neutralizer) is a water-soluble protein using a recombinant gene and is a dark brown liquid. A recombinant gene protein based on the chemical structure of clindamycin hydrochloride. The active center of its gene fragment can destroy the chemical structure formula of clindamycin hydrochloride and lose the antimicrobial properties of the drug after ring-opening/chain breaking.When doing sterility check of antibiotics, use a manual syringe to absorb sterile water and inject it into the drug vial, shake well, dissolve, and then suck it out. Add to 500ml solution of 0.9% sodium chloride, shake well, do not dissolve with the needle on the incubator, input, avoid high concentration of solution through the filter membrane, resulting in difficult to rinse thoroughly.Here, it is emphasized again: when doing sterile examination of antibiotics, it is necessary to inject sterile water into the manual syringe to dissolve the sample, and then transfer the dissolved sample to 500ml solution of 0.9% sodium chloride, so that the sample will not cause local concentration too high, difficult to wash thoroughly through the filter membrane.During sterility test, take 3ml of enzyme and add 2ml of sterile water and shake well to make a diluent of Clindamycin hydrochloride (neutralizer). Take 2ml of enzyme diluent and add 1500ml of rinsing solution and shake well. After the rinse solution has washed the filter membrane of the incubator, the pump is exhausted. Use a manual syringe to Pierce the respiratory mouth of the three incubators, add 1ml of diluting enzyme, spread the enzyme on the entire surface of the filter membrane as much as possible, rest for 10 minutes, and make the high concentration of enzyme fully contact with the filter membrane of the incubator, so as to destroy (neutralize and inactivate) the residual clindamycin hydrochloride drug on the filter membrane, and then pump into the corresponding medium and shake well. Positive pairs were treated with 1ml of E. coli (100CFU/ml).Adding 2ml dilution of clindamycin hydrochloride (neutralizer) to the rinse solution can remove a small amount of antimicrobial properties of clindamycin hydrochloride remaining in the filter membrane.Adding 1ml dilution of clindamycin hydrochloride (neutralizer) to three incubators can remove a small amount of antimicrobial activity of clindamycin hydrochloride remaining on the inner walls of the incubators and on the surface of the filter membrane.Shake the positive pair gently once a day in the morning and afternoon.Customers can do methodological verification according to the above, but also according to the actual operation of the verification... Read More | Biochemical Test:SDS-PAGE (purity > 80%); Western blot with patient sample.Calculated Isoelectric Point:pH 6.47 | Purity>95% SDS-PAGE.FunctionB Cell Activating Factor Receptor (BAFF-R), also named tumor necrosis factor receptor superfamily member 13C, is a member of the TNFR superfamily. It is highly expressed in spleen, lymph node, and resting B cells and to some extent in activated B cells, resting CD4+ Purity>95% SDS-PAGE.FunctionB Cell Activating Factor Receptor (BAFF-R), also named tumor necrosis factor receptor superfamily member 13C, is a member of the TNFR superfamily. It is highly expressed in spleen, lymph node, and resting B cells and to some extent in activated B cells, resting CD4+ cells and peripheral blood leukocytes. BAFF receptor is a type III transmembrane protein containing a single extracellular phenylalanine-rich domain and binds with high specificity to BAFF (TNFSF13B). It enhances B-cell survival in vitro and is a regulator of the peripheral B-cell population. BAFF receptor/BAFF signaling plays a critical role in B cell survival and maturation... Read More | Purity>97% SDS-PAGE and HPLC analyses. FunctionLA-PF4 stimulates DNA synthesis, mitosis, glycolysis, intracellular cAMP accumulation, prostaglandin E2 secretion, and synthesis of hyaluronic acid and sulfated glycosaminoglycan. It also stimulates the formation and secretion of plasminogen Purity>97% SDS-PAGE and HPLC analyses. FunctionLA-PF4 stimulates DNA synthesis, mitosis, glycolysis, intracellular cAMP accumulation, prostaglandin E2 secretion, and synthesis of hyaluronic acid and sulfated glycosaminoglycan. It also stimulates the formation and secretion of plasminogen activator by human synovial cells. NAP-2 is a ligand for CXCR1 and CXCR2, and NAP-2, NAP-2(73), NAP-2(74), NAP-2(1-66), and most potent NAP-2(1-63) are chemoattractants and activators for neutrophils. TC-1 and TC-2 are antibacterial proteins, in vitro released from activated platelet alpha-granules. CTAP-III(1-81) is more potent than CTAP-III desensitize chemokine-induced neutrophil activation.Post-translationalProteolytic removal of residues 1-9 produces the active peptide connective tissue-activating peptide III (CTAP-III) (low-affinity platelet factor IV (LA-PF4)). Proteolytic removal of residues 1-13 produces the active peptide beta-thromboglobulin, which is released from platelets along with platelet factor 4 and platelet-derived growth factor. NAP-2(1-66) is produced by proteolytical processing, probably after secretion by leukocytes other than neutrophils. NAP-2(73) and NAP-2(74) seem not be produced by proteolytical processing of secreted precursors but are released in an active form from platelets... Read More | Format:1-ComponentEnzyme:Horseradish peroxidase |