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商品編號


AG-40B-0107-C010



品牌


Adipogen



公司


Adipogen



公司分類(lèi)


Immunology



Size

10 ?g


商品信息


More Information



Product Details



Synonyms

MultimericCD40L?; ACRP30
headless
:CD40L; ACRP30
headless
:CD154; ACRP30
headless
:TNFSF5;
ADI
POQ-CD40L



Product Type

Protein



Properties



Source/Host

CHO cells



Sequence

Rat CD40L (aa 115-260) is fused at the N-terminus to mouse ACRP30
headless
(aa 18-111) and a FLAG
?
-tag.



Crossreactivity

Human
Mouse
Rat



Specificity

Binds to rat, human and mouse CD40.



BIOLOG
ical Activity

Induces B cell activation (as demonstrated by dose-dependent upregulation of CD86).



MW

~35-40kDa



Purity

≥95% (SDS-PAGE)



Endotoxin Content

<0.02eu mu;g="" purified="" protein="" (lal="" test;="" lonza).="">0.02eu>



Concentration

0.1mg/ml after reconstitution.



Reconstitution

Reconstitute with 100μl sterile water.



Formulation

Lyophilized. Contains PBS.



Other Product Data


Uniprot link Q9Z2V2: CD40L (rat)

FLAG is a registered trademark of
Sigma-Aldrich
Co.




Shipping and Handling



Shipping

BLUE ICE



Short Term Storage

+4°C



Long Term Storage

-20°C



Handling Advice

After reconstitution, prepare aliquots and store at -20°C.
Avoid freeze/thaw cycles.
PBS containing at least 0.1% BSA should be used for further dilutions.



Use/St
ABI
lity

Stable for at least 6 months after receipt when stored at -20°C.



Documents



MSD
S


Download PDF



Product Specification Sheet



Datasheet


Download PDF





MultimericCD40L? is a high activity construct in which two trimeric CD40 ligands are artificially linked via the collagen domain of ACRP30. This construct very effectively simulates the natural membrane-assisted aggregation of CD40L
in vivo
. It provides a simple and equally potent alternative to CD40L+enhancer combinations. MultimericCD40L? has been shown to suppress alum-induced IL-1β release and caspase-1 activation in a dose-, CD40- and time dependent manner, without affecting BMDM (Bone marrow-derived macrophages) vi
ABI
lity. It also effectively suppressed the inflammasome function triggered by NLRP3 activators. The secretion of caspase-1 independent inflammatory mediators has been shown to be unaltered or even enhanced.