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Product Name: A2M / Alpha-2-Macroglobulin Antibody
Species Reactivity: Human, Rat
Tested Applications: ELISA, IHC, WB
Applications: A2M / Alpha-2-Macroglobulin Antibody can be used for ELISA, Immunohistochemistry in paraffin embeded tissues starting at 10 μg/mL, and Western Blotting starting at 1μg/mL.
User Note: Optimal dilutions for each application to be determined by the researcher.
Predicted Molecular Weight:
Immunogen: Synthetic peptide corresponding to C-Terminal residues of human A2M (Alpha-2-macroglobulin precursor)
Host Species: Rabbit
Purification: Immunoaffinity Chromatography
Physical State:
CAS NO.: 413611-93-5
Product: 10074-G5
Buffer: PBS, 0.01% sodium azide, 50% glycerol.
Concentration: 0.5 mg/ml
Storage Conditions: Antibody may be stored short term at 4˚C, long term aliquot and store at -20˚C, avoid freeze thaw cycles.
Clonality: Polyclonal
Conjugate: Unconjugated
Alternate Names: A2M, CPAMD5, A2MD, FWP007, Alpha-2-M, Alpha-2-macroglobulin, S863-7
Accession NO.: P01023
Protein Ino: 308153640
Official Symbol: A2M
Geneid: 2
Background:
PubMed ID:http://aac.asm.org/content/51/11/4209.abstract

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Markers and mechanisms. A single of them, which we termed `PC-Pool', identifies pan-cancer markers as
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Aranodes, and juxtaparanodes. Alterations ofthe axo-glial interaction contribute to the etiology of many neurological diseases.
Eration of JAK2V617F-positive cells [21]. Consequently, combinations that synergisticallyPLOS OneEration of JAK2V617F-positive cells [21]. Therefore,
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Se antioxidants had pretty restricted effects on DNA harm and repair for these iPS cells
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Et al., 1992) to produce vpr/ RAG1+/- mice in F1 generation. The F1 vpr transgenic
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Hed by means of modulation of regulatory pathways, attaining an JNK3 site insulin-like impact: augmentingHed
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The mechanisms underlying the lower in severity of CIA following administration of GMSCs. GMSC injection
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Es Sp1-6 and Sp1-7) was deleted, an further reduction in luciferase activity was observed. These
Entiation and memory formation [51]. Also, RCAN1-1S overexpression within the hippocampal neuronal cell line HT22
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Markers and mechanisms. A single of them, which we termed `PC-Pool', identifies pan-cancer markers as
Sembly, 2014 (un.org/en/ga/search/view_doc.asp?symbol=A/ RES/69/1, accessed 25 November 2014). 5. Statistical Tables on Overseas Filipino Workers
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Xperiment comparing the polypeptide SDS-PAGE profiles of uninduced and IPTG-induced cultures for F1, LcrV and
Of S. spinosa Lu106 exhibited a development defect relative to that with the wild form.
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Assay from the studied drugs in pure forms and pharmaceutical formulations.Conflicts of InterestsThere is no
Autophagy. Therefore we conclude that vacuolar lipase activity is, for by far the most element,
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Nto the pathogenesis of aortic stenosis.AcknowledgmentsFunded by grants from the American Heart Association (AHA: 11GRNT7900016)
G of oxidative phosphorylation, high amplitude mitochondrial swelling and outer membrane rupture (Di Lisa et
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Ther up-regulated in prostate cancer [9], also as non-prostatic malignancies including gastric cancer [10]. PSCA
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Ysis of pheromone-dependent gene transcription in WT and reg1 cells. CellsYsis of pheromone-dependent gene transcription
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Sets we discover that there is a statistical difference (P = 2.eight ?1026), confirming that
Te-sex pheromonal odors: 6-OHDA lesions of DA terminals within this area abolished the hardwired D1
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