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Product Name: Argininosuccinate Synthetase 1 Antibody
Species Reactivity: Human
Tested Applications: ELISA, IF, IHC-P, IP, WB
Applications: ELISA: antibody detection limit dilution 1:64000. Western Blot: Approx 45kDa band observed in Human Kidney lysates (calculated MW of 46.5kDa according to NP_000041.2 and NP_446464.1). Recommended concentration: 0.01-0.03μg/ml. Immunohistochemistry: In paraffin embedded Human Kidney shows textured cytoplasm staining in PCT. Recommended concentration, 2-4μg/ml. Immunofluorescence: A customer has reported this antibody works well in IF.Immunoprecipitation: This antibody has been successfully used in IP from BAEC cells as described in the following paper: Corbin et al, Bioche
User Note:
Predicted Molecular Weight:
Immunogen: Argininosuccinate Synthetase 1 antibody was raised against a 17 amino acid synthetic peptide near the internal region of Argininosuccinate Synthetase 1.
Host Species: Goat
Purification: Argininosuccinate Synthetase 1 antibody was purified from goat serum by ammonium sulphate precipitation followed by antigen affinity chromatography using the immunizing peptide.
Physical State: Liquid
CAS NO.: 1381289-58-2
Product: Ribocil
Buffer: Argininosuccinate Synthetase 1 antibody is supplied in Tris saline, 0.02% sodium azide, pH 7.3 with 0.5% bovine serum albumin.
Concentration: 500 ug/mL
Storage Conditions: Aliquot and store at -20˚C. Minimize freezing and thawing.
Clonality: Polyclonal
Conjugate: Unconjugated
Alternate Names: ASS1, Argininosuccinate synthetase 1, ASS, CTLN1, citrulline–aspartate ligase
Accession NO.: NP_000041.2 , NP_446464.1
Protein Ino: 53759107
Official Symbol: ASS1
Geneid: 445
Background:
PubMed ID:http://aac.asm.org/content/53/4/1679.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.
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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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Cript.Acknowledgments This study was funded by the H.L. Lauterbach Fund and the NOFAR Grant from
Es Sp1-6 and Sp1-7) was deleted, an further reduction in luciferase activity was observed. These
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Ession, suggesting that the enhanced vascular reactivity to phenylephrine induced byEssion, suggesting that the elevated
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
That A-ring modifications seem to become tolerable for yielding biologically intriguingThat A-ring modifications seem to
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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
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