Phone: +46 (0)935 33000   Mail: orders@agrisera.com
Choose currency:
 
Log in Create new acount About AgriseraContact usCredit card paymentDistributorsOrdering infoPricing Agrisera blog

Antibodies for:

Plant/Algal cell antibodies Animal cell antibodies

Search product

Search by species
Shopping cart
There are no articles in your shopping cart yet.

 

   New products

 

   Custom antibodies

   Western blot

   Quick order

   News letter







 

Plant/Algal cell antibodies / Conifers


UGPase | UDP-glucose pyrophosphorylase (cytoplasm marker)

Art no: AS05 086
Price: 310
Order:
Qty: 

Shipping:
World-wide

Info More information Add review Related products Product suggestions Tell a friend

product information

background  

UDP-glucose pyrophosphorylase (UGPase, UDPGP) E.C=2.7.7.9.  is a key enzyme of synthesis of sucrose, cellulose and other saccharides.

immunogen  

recombinant UGPase overexpressed and purified from E.coli Q43772 

antibody format  

rabbit

polyclonal

serum,

lyophilized

quantity  

200 µl,

for reconstitution add 200 µl of sterile water.

storage  

store lyophilized/reconstituted at -20°C; once reconstituted make aliquots to avoid repeated freeze-thaw cycles. Please, remember to spin tubes briefly prior to opening them to avoid any losses that might occur from lyophilized material adhering to the cap or sides of the tubes.

tested applications  

western blot (WB)

related products  

For cytoplasmic marker for Chlamydomonas reinhardtii - please check NAB1

collection of antibodies to carbohydrate metabolism

recommended secondary antibody

additional information  

cellular [compartment marker] of cytoplasm, UGPse is a cytoplasmic protein Martz et al. (2002)

application information

recommended dilution  

1: 1000 - 1: 3000  with standard ECL (WB)

expected | apparent MW  

51.6 kDa

confirmed reactivity  

Arabidopsis thaliana, C. annuum, C. sativus, F. arundinacea,  Hordeum vulgare, L. esculentum, L. chilense, N. tabacum, Oryza sativa, Populus sp., S. tuberosum, S. sogarandinum,

predicted reactivity  

dicots including: Gossipium hirsutum, Ricinus communis, Solanum tuberosum, Vitis vinifera, monocots including: Saccharum officinarumZea mays, trees: Populus tremula, conifers: Pinus taeda

not reactive in  

no confirmed exceptions from predicted reactivity known in the moment

additional information  

this antibody detectes 1 ng of UGPase in a western blot

selected references  

Yu et al. (2011). Comparative proteomic study reveals the involvement of diurnal cycle in cell division, enlargement and starch accumulation in developing endosperm of Oryza sativa. J of Proteome Res. Nov, ahead of print

Estavillo et al. (2011). Evidence for a SAL1-PAP Chloroplast Retrograde Pathway That Functions in Drought and High Light Signaling in Arabidopsis. Plant Cell Nov. 29 (ahead of print).

Sullivan et al. (2007). In Vivo Phosphorylation Site Mapping and Functional Characterization of Arabidopsis Phototropin 1. Mol. Plant-published on-line.

Kuras et al. (2007). A specific c-type cytochrome maturation system is required for oxygenic photosynthesi. PNAS 104:9906-9910.


UGPase

 A 1-year-old greehouse grown plant was dissectedinto different tissues, which were then used for enzyme assays and immunoblot analyses. Equal amounts of total protein (7.5 μg) were loaded on each lane. SDS-PAGE was run on a 7.5% gel. Immunoblot was done using Amersham PVDF transfer membrane. Primary antibodies against barley UGPase were used in 1: 1000 dilution. Secondary antibodies (Amersham ECL Rabbit IgG, HRP-Linked Whole Antibody from donkey) were used at 1:10 000.

ff - female flower, mf - male flower, yl - young leaf, ml - mature leaf, sbk - stem bark, sph - stem phloem and cambium, sxy - stem xylem, rxy - root xylem

 

western blot using plant anti-UGPase antibodies

15 µg of  total  soluble protein  extract from leaves and stems of  Solanum tuberosum (1),  Solanum sogarandinum (2),   Lycopersicum esculentum (3)Lycopersicum chilense  (4) , Arabidopsis thaliana (5) , Cucumis sativus (6)Festuca arundinacea  (7) , Nicotiana tabacum (8) and Capsicum annuum (9)  were separated  on 10% SDS-PAGE and blotted onto nitrocellulose .  After blocking with 5% milk in TBST , blots were incubated with the primary antibody at a dilution of 1:1500 in TBST for 1h  at room temperature. Following incubation and wash steps, blots were incubated with SIGMA secondary Anti-Rabbit IgG , Alkaline Phosphatase Conjugate for 1 hour at a dilution of 1:40000 . Blots were developed with the alkaline phosphatase detection system using NBT/BCIP (SIGMA).

Courtesy of Bartosz Szabala, Institute of Plant Genetics, Polish Academy of Science .


||| For applications or usage on species others than stated above Agrisera offers a payment-after-testing option. To learn more about this or for any questions on this product, please use the LiveChat option in the left menue bar or contact us at  support@agrisera.com



Save as PDF


Bookmark and Share

 
Agrisera AB Box 57, SE-911 21 Vännäs, SWEDEN | Phone: +46(0)935 33000 | Fax: +46(0)935 33044 | VAT nr: SE556263276901 |
OLAW/NIH nr: A5783-01 | orders@agrisera.com