chlorotoxin (Alomone Labs)


Structured Review

Chlorotoxin, supplied by Alomone Labs, used in various techniques. Bioz Stars score: 93/100, based on 14 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/chlorotoxin/product/Alomone Labs
Average 93 stars, based on 14 article reviews
Price from $9.99 to $1999.99
Images
1) Product Images from "A ligand-mediated nanovector for targeted gene delivery and transfection in cancer cells"
Article Title: A ligand-mediated nanovector for targeted gene delivery and transfection in cancer cells
Journal: Biomaterials
doi: 10.1016/j.biomaterials.2008.10.003

Figure Legend Snippet: 1 H NMR spectra showing characteristic peaks of the chlorotoxin peptide (CTX) at 2.60–3.10 and 3.65–3.80 ppm, SIAX-functionalized P-PEG polymer (P-PEG-SIAX) at 3.60–3.65 for the -O-CH2-CH2- repeating unit of PEG and at 2.50–3.10
Techniques Used: Nuclear Magnetic Resonance

Figure Legend Snippet: Nanovector preparation scheme. (a) PEGylation of PEI polymer and modification with Alexa Fluor 647 fluorophores (AF). (b) P-PEG-AF modification with SIAX, modification of chlorotoxin (CTX) with traut’s reagent to produce free thiols on peptide
Techniques Used: Modification
2) Product Images from "Chlorotoxin Labeled Magnetic Nanovectors for Targeted Gene Delivery to Glioma"
Article Title: Chlorotoxin Labeled Magnetic Nanovectors for Targeted Gene Delivery to Glioma
Journal: ACS nano
doi: 10.1021/nn1008512

Figure Legend Snippet: Enhanced delivery of GFP encoding DNA to C6 glioma cells in vivo using chlorotoxin labeled NPs. a) Xenogen images of tumors, livers, kidneys, and spleens from C6 xenograft tumor bearing mice, harvested 48 hrs after treatment, indicating GFP fluorescence
Techniques Used: In Vivo, Labeling, Mouse Assay, Fluorescence
3) Product Images from "Specific targeting of brain tumors with an optical/MR imaging nanoprobe across the blood brain barrier"
Article Title: Specific targeting of brain tumors with an optical/MR imaging nanoprobe across the blood brain barrier
Journal:
doi: 10.1158/0008-5472.CAN-09-1157

Figure Legend Snippet: In vivo NIRF imaging of autochthonous medulloblastoma tumors in genetically engineered ND2:SmoA1 mice. ( a and b ) Fluorescence imaging of medulloblastoma tumors in ND2:SmoA1 mice injected with either NPCP-Cy5.5-CTX or NPCP-Cy5.5, or receiving no injection
Techniques Used: In Vivo, Imaging, Mouse Assay, Fluorescence, Injection

Figure Legend Snippet: Histological examination of mouse cerebellum 5 days post injection of NPCP-Cy5.5-CTX or NPCP-Cy5.5. ( a ) The H E stained cerebellum section of symptomatic ND2:SmoA1 mice confirming presence of medulloblastoma, and ( b ) for comparison, the cerebellum
Techniques Used: Injection, Staining, Mouse Assay

Figure Legend Snippet: Biodistribution of nanoprobes. Accumulation of nanoprobes in various tissues assessed by NIRF signal measurements of tissues/organs excised from ND2:SmoA1 mice receiving no injection and 120 hours after receiving injection of either targeting NPCP-Cy5.5-CTX
Techniques Used: Mouse Assay, Injection

Figure Legend Snippet: Synthesis and characterization of NPCP-Cy5.5-CTX nanoprobes. Chemical reaction schematic for the syntheses of ( a ) PEG-grafted chitosan, ( b ) sulfhydryl functionalization of chlorotoxin (CTX), and ( c ) chlorotoxin and Cy5.5 conjugation to NPCP. ( d ) Summary
Techniques Used: Conjugation Assay
4) Product Images from "Properties of single-channel and whole cell Cl− currents in guinea pig detrusor smooth muscle cells"
Article Title: Properties of single-channel and whole cell Cl− currents in guinea pig detrusor smooth muscle cells
Journal: American Journal of Physiology - Cell Physiology
doi: 10.1152/ajpcell.00327.2018

Figure Legend Snippet: Niflumic acid and DIDS inhibit outwardly rectifying Cl − current in detrusor smooth muscle (DSM) cells while chlorotoxin does not. A – C : normalized leak-unsubtracted time courses of Cl − currents measured at +100 mV caused by repetitive 1 s voltage ramps from −100 mM to +100 mV. Data were normalized to the first data point value. Arrow indicates the beginning of local perfusion (also marked as “Flow”). Isochronic drug applications show inhibitory effects of niflumic acid (NA, n = 5, N = 3) ( A ) and DIDS ( n = 4, N = 3) ( B ), and no effect of chlorotoxin (CTX, n = 5, N = 3) ( C ) on Cl − current.
Techniques Used:
5) Product Images from "Properties of single-channel and whole cell Cl− currents in guinea pig detrusor smooth muscle cells"
Article Title: Properties of single-channel and whole cell Cl− currents in guinea pig detrusor smooth muscle cells
Journal: American Journal of Physiology - Cell Physiology
doi: 10.1152/ajpcell.00327.2018

Figure Legend Snippet: Niflumic acid and DIDS inhibit outwardly rectifying Cl − current in detrusor smooth muscle (DSM) cells while chlorotoxin does not. A – C : normalized leak-unsubtracted time courses of Cl − currents measured at +100 mV caused by repetitive 1 s voltage ramps from −100 mM to +100 mV. Data were normalized to the first data point value. Arrow indicates the beginning of local perfusion (also marked as “Flow”). Isochronic drug applications show inhibitory effects of niflumic acid (NA, n = 5, N = 3) ( A ) and DIDS ( n = 4, N = 3) ( B ), and no effect of chlorotoxin (CTX, n = 5, N = 3) ( C ) on Cl − current.
Techniques Used: