chemical phosphorylation reagent i (cpr i) -九游会ag

oligo labeling dyes
chemical phosphorylation reagent i (cpr i)
product id: 6001-100mg
835元/100mg
products

chemical phosphorylation reagent i (cpr i)

cat#

size

price

mw

abs

em

soluble in

storage 

6001

1 g

$395

656.77

n/a

n/a

mecn

f/d/l

 

features and biological applications
this reagent can be used to create the 3'-phosphate by adding it as the first addition to the support in labeling oligonucleotides with fluorescent dyes. after ammonia deprotection the oligo will have the 3'-phosphate attached to the 2nd base added during synthesis. both the support base and the cpr are cleaved. the dmt-group is removed during the ammonium hydroxide deprotection and thus is not available for poly-pak purification.
 
references

1.  xu y, lee sa, kutateladze tg, sbrissa d, shisheva a, prestwich gd. (2006) chemical synthesis and molecular recognition of phosphatase-resistant analogues of phosphatidylinositol-3-phosphate. j am chem soc, 128, 885.

2.  ohkubo a, ezawa y, seio k, sekine m. (2004) o-selectivity and utility of phosphorylation mediated by phosphite triester intermediates in the n-unprotected phosphoramidite method. j am chem soc, 126, 10884.

3.  tsuruoka h, shohda k, wada t, sekine m. (2000) synthesis and conformational properties of oligonucleotides incorporating 2'-o-phosphorylated ribonucleotides as structural motifs of pre-trna splicing intermediates. j org chem, 65, 7479.

4.  olejnik j, krzymanska-olejnik e, rothschild kj. (1996) photocleavable biotin phosphoramidite for 5'-end-labeling, affinity purification and phosphorylation of synthetic oligonucleotides. nucleic acids res, 24, 361.

5.  mora n, lacombe jm, pavia aa. (1995) a new approach to phosphoserine, phosphothreonine and phosphotyrosine synthons and to thiophospho analogs. stepwise synthesis of mono- and multiphosphorylated phosphopeptides related to src-protein kinase. int j pept protein res, 45, 53.

6.  boumendjel a, miller sp. (1994) synthesis of sphingosine-1-phosphate and dihydrosphingosine-1-phosphate. j lipid res, 35, 2305.

7.  kitas e, kung e, bannwarth w. (1994) chemical synthesis of o-thiophosphotyrosyl peptides. int j pept protein res, 43, 146.

8.  tegge w, ballou ce. (1992) syntheses of d-myo-inositol 1,4,5-trisphosphate affinity ligands. carbohydr res, 230, 63.

9.  perich jw, reynolds ec. (1991) fmoc/solid-phase synthesis of tyr(p)-containing peptides through t-butyl phosphate protection. int j pept protein res, 37, 572.

10.   lacombe jm, andriamanampisoa f, pavia aa. (1990) solid-phase synthesis of peptides containing phosphoserine using phosphate tert.-butyl protecting group. int j pept protein res, 36, 275.


description
name chemical phosphorylation reagent i (cpr i)
cat# 6001-100mg cas# n/a
storage# −20°c desiccated and minimize light exposure shelf life# 12 months
ex(nm)# n/a em(nm)# n/a
mw# 656.77 solvent# mecn,dmso
name chemical phosphorylation reagent i (cpr i)
cat# 6001-100mg
cas# n/a
storage# −20°c desiccated and minimize light exposure
shelf life# 12 months
ex(nm)# n/a
em(nm)# n/a
mw# 656.77
solvent# mecn,dmso
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