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Filtered Search Results
ABclonal Technology ABflo 594 Rabbit anti- CD19
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Involved in several processes including B-1 B cell differentiation positive regulation of phosphatidylinositol 3-kinase activity and positive regulation of release of sequestered calcium ion into cytosol Acts upstream of or within B cell receptor signaling pathway Located in external side of plasma membrane Is integral component of plasma membrane Is expressed in liver and spleen Human ortholog(s) of this gene implicated in common variable immunodeficiency Orthologous to human CD19 (CD19 molecule)
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Jackson Immuno Research Labs AMCA-AffiniPure F(ab')2 Fragment Rabbit Anti-Goat IgG (H+L) (min X Hu Sr Prot)
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AMCA-AffiniPure F(ab')2 Fragment Rabbit Anti-Goat IgG (H+L) (min X Hu Sr Prot)
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Sigma Aldrich Fine Chemicals Biosciences SIGMA ALDRICH FINE CHEMICALS BIOSCIENCES
NC3972427 ANTI-IL6R AB IN RBT 100UG
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Aat Bioquest AAT BIOQUEST
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NC4021538 RABBIT ANTI-ALEXA FLUOR 647 AN
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Rockland Immunochemicals ROCKLAND IMMUNOCHEMICALS
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NC4022233 5MG OF RABBIT IGG FAB
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Jackson Immuno Research Labs Alexa Fluor 647-AffiniPure Rabbit Anti-Goat IgG F(ab')2 Fragment Specific (min X Hu Sr Prot)
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Alexa Fluor 647-AffiniPure Rabbit Anti-Goat IgG F(ab')2 Fragment Specific (min X Hu Sr Prot)
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Cayman Chemical AF-353hydrochlorIde 1mg
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A dual P2X3 and P2X2/3 receptor antagonist (IC50s = 10 and 79.4 nM, respectively); selective for P2X3 and P2X2/3 over P2X1, P2X2, P2X4, P2X5, and P2X7 (IC50 = >10 µM for all); inhibits calcium flux in CHO-K1 cells expressing the rat P2X3 receptor and in 1321N1 cells expressing the human P2X3 and P2X2/3 receptors (IC50s = 8.91, 8.71, and 38.9 nM, respectively); decreases the electrical signals in the detrusor, but not striated, muscle of the bladder in female rats
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eMolecules 21262-04-4 | ChemScene | 2-Chloro-N-(4-fluorophenyl)propanamide | 100mg | 686210337 | CS-0307831 | MFCD04626493 | 201.63 | C9H9ClFNO
Medchem Express | (-)-Gallocatechin gallate | 5mg | 446275141 | HY-N0522 | 4233-96-9 | MFCD00214298 | 458.375 | C22H18O11
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eMolecules 1209458-16-1 | Ambeed | 4-Bromo-N-methylpyrimidin-2-amine | 250mg | 552682427 | A262751 | MFCD13193672 | 188.028 | C5H6BrN3
Pharmablock | 1-(benzenesulfonyl)-6-bromo-1H-pyrrolo[32-b]pyridine | 25mg | 713714516 | PBZ3295 | 1305325-23-8 | MFCD20487024 | 337.190 | C13H9BrN2O2S
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eMolecules 27469-61-0 | Ambeed | 1-(Bis(4-chlorophenyl)methyl)piperazine | 250mg | 561133930 | A162981 | MFCD00191212 | 321.25 | C17H18Cl2N2
Ambeed | 2-(4H-124-Triazol-4-yl)ethanol | 250mg | 528956897 | A924202 | 66760-19-8 | MFCD03265455 | 113.120 | C4H7N3O
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Meridian Life Science RABBIT ANTI E. COLI ALL AG'S
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E. coli (O & K antigens)
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Cayman Chemical TMEM16A RabbIt MoncLNal nt
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A PEGylated form of DSPE
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ABclonal Technology STIM1 Rabbit PolymAb
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This gene encodes a type 1 transmembrane protein that regulates Ca2 influx through store-operated Ca2 channels (SOCs) after intracellular Ca2 depletion Located in the imprinted gene domain of 11p15 5 a tumor-suppressor region alterations in this area are linked to Beckwith-Wiedemann syndrome Wilms tumor rhabdomyosarcoma and cancers of the lung ovarian and breast The gene may also play a role in malignancies disease in this region and early hematopoiesis by mediating attachment to stromal cells Mutations are associated with fatal classic Kaposi sarcoma immunodeficiency from defects in store-operated calcium entry ectodermal dysplasia and tubular aggregate myopathy This gene is near the RRM1 gene with alternative splicing producing multiple transcript variants
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Bethyl Laboratories, Inc RABBIT ANTI-BOVINE WHOLE SERUM
Rabbit anti-Bovine Whole Serum Antibody
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ABclonal Technology SFTPC Rabbit PolymAb
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This gene encodes the pulmonary-associated surfactant protein C (SPC) an extremely hydrophobic surfactant protein essential for lung function and homeostasis after birth Pulmonary surfactant is a surface-active lipoprotein complex composed of 90% lipids and 10% proteins which include plasma proteins and apolipoproteins SPA SPB SPC and SPD The surfactant is secreted by the alveolar cells of the lung and maintains the stability of pulmonary tissue by reducing the surface tension of fluids that coat the lung Multiple mutations in this gene have been identified which cause pulmonary surfactant metabolism dysfunction type 2 also called pulmonary alveolar proteinosis due to surfactant protein C deficiency and are associated with interstitial lung disease in older infants children and adults Alternatively spliced transcript variants encoding different protein isoforms have been identified
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