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|Tested species reactivity||Bovine, Dog, Deer, Horse, Cat, Guinea pig, Goat, Human, Primate, Pig, Rabbit, Rat|
|Published species reactivity||Dog, Rat, Pig, Bovine, Human, Mouse|
|Host / Isotype||Mouse / IgG1|
|Contains||0.09% sodium azide|
|Storage Conditions||4°C or -20°C if preferred|
|Tested Applications||Dilution *|
|Flow Cytometry (Flow)||1/50 - 1/100|
|Immunohistochemistry (Paraffin, Frozen) (IHC (P, F))||1/100 - 1/200|
* Suggested working dilutions are given as a guide only. It is recommended that the user titrate the product for use in their own experiment using appropriate negative and positive controls.
This product requires protein digestion pre-treatment of paraffin sections using trypsin or pronase. A suggested positive control is human spleen. For FACS analysis, use 10ul of the suggested working dilution to label 1x10^6 cells in 100ul.
The protein encoded by this gene is a member of the S100 family of proteins containing 2 EF-hand calcium-binding motifs. S100 proteins are localized in the cytoplasm and/or nucleus of a wide range of cells, and involved in the regulation of a number of cellular processes such as cell cycle progression and differentiation. S100 genes include at least 13 members which are located as a cluster on chromosome 1q21. This protein may function in the inhibition of casein kinase and as a cytokine. Altered expression of this protein is associated with the disease cystic fibrosis.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Polymeric embolization coil of bilayered polyvinyl alcohol strand for therapeutic vascular occlusion: a feasibility study in canine experimental vascular models.
MA1-81381 was used in immunohistochemistry to test polyvinyl alcohol polymer coil as an endovascular embolic agent in a canine vascular model
|Jung SC,Choi SH,Cho HR,Lee TH,Kim TY,Jeong W,Rhee K,Jho JY,Kim JH,Han MH||Journal of vascular and interventional radiology : JVIR (26:117)||2015|
Xenotransplantation of human unrestricted somatic stem cells in a pig model of acute myocardial infarction.
MA1-81381 was used in immunohistochemistry to study whether xenotransplantation with human CD34-/CD45- unrestricted somatic stem cells is of therapeutic benefit in a porcine model of acute myocardial infarction
|Gahremanpour A,Vela D,Zheng Y,Silva GV,Fodor W,Cardoso CO,Baimbridge F,Fernandes MR,Buja LM,Perin EC||Xenotransplantation (20:110)||2013|
Gene expression profile of vascular endothelial growth factor (VEGF) and its receptors in various cell types of the canine lymph node using laser capture microdissection (LCM).
MA1-81381 was used in immunohistochemistry to study the expression of VEGF and its receptors in a range of cell types in normal canine lymph nodes.
|Jais A,Klein D,Wolfesberger B,Walter I||Veterinary immunology and immunopathology (140:207)||2011|
The performance of photooxidatively crosslinked acellular bovine jugular vein conduits in the reconstruction of connections between pulmonary arteries and right ventricles.
MA1-81381 was used in immunohistochemistry to evaluate photooxidatively crosslinked acellular bovine jugular vein conduits in vascular reconstruction
|Lü WD,Zhang M,Wu ZS,Hu TH,Xu ZJ,Liu W,Hu YR||Biomaterials (31:2934)||2010|
Chronic intake of a high-cholesterol diet resulted in hepatic steatosis, focal nodular hyperplasia and fibrosis in non-obese mice.
MA1-81381 was used in immunohistochemistry to investigate the influence of high-cholesterol food on liver function in normal mice
|Sumiyoshi M,Sakanaka M,Kimura Y||The British journal of nutrition (103:378)||2010|
Characterization of a preclinical model of chronic ischemic wound.
MA1-81381 was used in immunohistochemistry to develop and evaluate a preclinical porcine model of chronic ischemic wound
|Roy S,Biswas S,Khanna S,Gordillo G,Bergdall V,Green J,Marsh CB,Gould LJ,Sen CK||Physiological genomics (37:211)||2009|
Insulin increases resistance to burn wound infection-associated sepsis.
MA1-81381 was used in flow cytometry to investigate the therapeutic efficacy of insulin on the treatment of sepsis
|Gauglitz GG,Toliver-Kinsky TE,Williams FN,Song J,Cui W,Herndon DN,Jeschke MG||Critical care medicine (38:202)||2010|