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Product Pathways - Protein Folding

HSP70 (6B3) Rat mAb #4873

Item# Description List Price Web Price Qty
4873S HSP70 (6B3) Rat mAb - 100 µl $372.00
$334.80
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*On-line ordering is for Canadian customers only. Web pricing is applicable only to orders placed online at www.neb.ca
VIEW COMPANION PRODUCTS HIDE COMPANION PRODUCTS
Application Dilution Species-Reactivity Sensitivity MW (kDa) Isotype
W Human, Monkey Endogenous 70 Rat IgG1
IP
IHC-P
IF-IC
F

Species cross-reactivity is determined by western blot.

Applications Key: W=Western Blotting, IP=Immunoprecipitation, IHC-P=Immunohistochemistry (Paraffin), IF-IC=Immunofluorescence (Immunocytochemistry), F=Flow Cytometry

Specificity / Sensitivity

HSP70 (6B3) Rat mAb detects endogenous levels of the inducible isoform of HSP70 protein. This antibody does not cross-react with other HSPs.  

Source / Purification

Monoclonal antibody is produced by immunizing animals with the recombinant human HSP70 expressed in E.coli.

Western Blotting

Western Blotting

Western blot analysis of extracts from HeLa and COS cells, using HSP70 (6B3) Rat mAb.

IHC-P (paraffin)

IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human breast carcinoma, using HSP70 (6B3) Rat mAb.

IHC-P (paraffin)

IHC-P (paraffin)

Immunohistochemical analysis of paraffin-embedded human lung carcinoma, showing cytoplasmic and nuclear localization using HSP70 (6B3) Rat mAb.


IF-IC

IF-IC

Confocal immunofluorescent analysis of HeLa cells, untreated (left) or heat shock-treated (right), using HSP70 (6B3) Rat mAb (green). Actin filaments have been labeled with Alexa Fluor® 555 phalloidin (red).

Flow Cytometry

Flow Cytometry

Flow cytometric analysis of Hela cells, using HSP70 (6B3) Rat mAb (blue) compared to a nonspecific negative control antibody (red).

Background

HSP70 and HSP90 are molecular chaperones expressed constitutively under normal conditions to maintain protein homeostasis and are induced upon environmental stress (1). Both HSP70 and HSP90 are able to interact with unfolded proteins to prevent irreversible aggregation and catalyze the refolding of their substrates in an ATP- and co-chaperone-dependent manner (1). HSP70 has a broad range of substrates including newly synthesized and denatured proteins, while HSP90 tends to have a more limited subset of substrates, most of which are signaling molecules. HSP70 and HSP90 often function collaboratively in a multi-chaperone system, which requires a minimal set of co-chaperones: HSP40, Hop, and p23 (2,3). The co-chaperones either regulate the intrinsic ATPase activity of the chaperones or recruit chaperones to specific substrates or subcellular compartments (1,4). When the ubiquitin ligase CHIP associates with the HSP70/HSP90 complex as a cofactor, the unfolded substrates are subjected to degradation by the proteasome (4). The biological functions of HSP70/HSP90 extend beyond their chaperone activity. They are essential for the maturation and inactivation of nuclear hormones and other signaling molecules (1,3). They also play a role in vesicle formation and protein trafficking (2).

Application References

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