"ASM" Related Products

Recombinant Human ASM, His-tagged

Cat.No.: ASM-3068H
Product Overview: Acid Sphingomyelinase (ASM)
Description: The protein encoded by this gene is a lysosomal acid sphingomyelinase that converts sphingomyelin to ceramide. The encoded protein also has phospholipase C activity. Defects in this gene are a cause of Niemann-Pick disease type A (NPA) and Niemann-Pick disease type B (NPB). Multiple transcript variants encoding different isoforms have been identified.
Source: E. Coli
Species: Human
Tag: His
Form: Supplied as lyophilized form in PBS,pH7.4, containing 5% sucrose, 0.01% sarcosyl.
Molecular Mass: 33.9kDa
Protein length: 631
Endotoxin: <1.0eu per 1ug (determined by the lal</1.0eu
Purity: >95%
Applications: SDS-PAGE, Western Blot (WB), ELISA (EIA), Immunoprecipitation (IP)
Notes: Small volumes of ASM recombinant protein may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice.
Storage: Avoid repeated freeze/thaw cycles. Store at 2-8 degree C for one month. Aliquot and store at -80 degree C for 12 months.Stability Test: The thermal stability is described by the loss rate of the targetprotein. The loss rate was determined by accelerated thermal degradation test,that is, incubate the protein at 37 degree C for 48h, and no obvious degradation andprecipitation were observed. (Referring from China Biological Products Standard,which was calculated by the Arrhenius equation.) The loss of this protein is lessthan 5% within the expiration date under appropriate storage condition.
Reconstitution: Reconstitute in sterile PBS, pH7.2-pH7.4.
Warning: This product is for research use only. Not for use in diagnostic or therapeutic procedures.
Gene Name: H19 H19, imprinted maternally expressed transcript (non-protein coding) [ Homo sapiens ]
Official Symbol: ASM
Synonyms: ASM; BWS; WT2; ASM1; PRO2605; D11S813E; LINC00008; NCRNA00008
Gene ID: 283120
MIM: 103280
UniProt ID: P17405
Chromosome Location: 11p15.4-p15.1

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