Citations

Citations

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4784 total record number 156 records this year

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Page 113 out of 479
4784 citations found

AgRP neurons control compulsive exercise and survival in an activity-based anorexia model

Miletta, MC;Iyilikci, O;Shanabrough, M;estan-Pea, M;Cammisa, A;Zeiss, CJ;Dietrich, MO;Horvath, TL;

Product: Diphtheria Toxin, Unnicked, from Corynebacterium diphtheriae

T cell-intrinsic role for Nod2 in protection against Th17-mediated uveitis

Napier, RJ;Lee, EJ;Davey, MP;Vance, EE;Furtado, JM;Snow, PE;Samson, KA;Lashley, SJ;Brown, BR;Horai, R;Mattapallil, MJ;Xu, B;Callegan, MC;Uebelhoer, LS;Lancioni, CL;Vehe, RK;Binstadt, BA;Smith, JR;Caspi, RR;Rosenzweig, HL;

Product: Pertussis Toxin from B. pertussis, Lyophilized in Buffer

Product: Cholera Toxin B Subunit (Choleragenoid) from Vibrio cholerae in Low Salt

  • 5.2. Retrograde tracer injections

    Rats were anaesthetized with an intraperitoneal injection of ketamine (40 mg/kg) and xylazine (2.5 mg/kg). The head was shaved and the rat was placed in a stereotaxic frame in the “flat skull” position. Following a subcutaneous injection of local anaesthetic, an incision was made along the midline of the scalp and using a dental drill a small craniotomy was made on the midline of the skull, 3 mm caudal to bregma. Under stereotaxic guidance, using Paxinos and Watson (2005) as a reference, a glass micropipette (tip diameter 5-10um) filled with Cholera-toxin subunit B (CTB, List Biological Laboratories) was lowered through a small hole in the dura, into the paraventricular thalamus to a depth of 6 mm below the exposed cortical surface. Over a 20-minute period, 50 nl of CTB was deposited via an automated air-pressure system (9 ms air pulses). …

    Product #104 – Cholera Toxin B Subunit (Choleragenoid) from Vibrio cholerae in Low Salt

Median preoptic area neurons are required for the cooling and febrile activations of brown adipose tissue thermogenesis in rat

da Conceio, EPS;Morrison, SF;Cano, G;Chiavetta, P;Tupone, D;

Product: Anti-Cholera Toxin B Subunit (Goat)

  • Neuroanatomical experimental procedures

    Following the 2 h cold or warm exposure, rats were deeply anesthetized with pentobarbital (80 mg/kg i.p.) and transcardially perfused with saline followed by 4% paraformaldehyde (PFA). The brains were removed and post-fixed in 4% PFA for 2 h and equilibrated overnight in 20% sucrose in 10 mM sodium phosphate buffered saline (PBS; pH 7.4) with 0.01% sodium azide. Serial coronal Sects. (30 µm) were cut with a freezing-stage microtome, collected sequentially in 6 sets, and stored in cryoprotectant with 0.01% sodium azide at − 20 °C. Sections containing the preoptic area were pre-incubated for 3 h in an antibody dilution solution (ADS) containing PBS, 0.3% Triton-X 100, 0.25% carrageenan, 0.02% NaN3, and 1% normal donkey serum, and incubated overnight at room temperature in ADS containing the primary antibodies for c-Fos (rabbit anti-c-Fos , 1:10 K, Calbiochem) and for CTb (goat anti-CTb, 1:10 K, List Biologicals). …

    Product #703 – Anti-Cholera Toxin B Subunit (Goat)

Go-sha-jinki-Gan Alleviates Inflammation in Neurological Disorders via p38-TNF Signaling in the Central Nervous System

Jiang, S;Baba, K;Okuno, T;Kinoshita, M;Choong, CJ;Hayakawa, H;Sakiyama, H;Ikenaka, K;Nagano, S;Sasaki, T;Shimamura, M;Nagai, Y;Hagihara, K;Mochizuki, H;

Product: Pertussis Toxin from B. pertussis, Lyophilized in Buffer

Decreased Histone Acetylation Levels at Th1 and Regulatory Loci after Induction of Food Allergy

Alashkar Alhamwe, B;Meulenbroek, LAPM;Veening-Griffioen, DH;Wehkamp, TMD;Alhamdan, F;Miethe, S;Harb, H;Hogenkamp, A;Knippels, LMJ;Pogge von Strandmann, E;Renz, H;Garssen, J;van Esch, BCAM;Garn, H;Potaczek, DP;Tiemessen, MM;

Product: Cholera Toxin (AZIDE-FREE) from Vibrio cholerae

  • 2.2. Experimental Design—Sensitization and Challenges

    Mice were sensitized and treated as described previously [32]. In short, after an acclimatization period of 5 days, mice in the sensitization group were sensitized intragastrically (i.g.) with 20 mg whey protein (DMV International, Veghel, The Netherlands) and 15 µg cholera toxin (List Biological Laboratories, Campbell, CA, USA), which was used as an adjuvant, in 0.5 mL phosphate-buffered saline (PBS), once a week, for 5 consecutive weeks.

    Product #100B – Cholera Toxin (AZIDE-FREE) from Vibrio cholerae

Amnion-Derived Multipotent Progenitor Cells Suppress Experimental Optic Neuritis and Myelitis

Khan, RS;Ross, AG;Willett, K;Dine, K;Banas, R;Brown, LR;Shindler, KS;

Product: Pertussis Toxin from B. pertussis, Lyophilized in Buffer

Molecular Fingerprint and Developmental Regulation of the Tegmental GABAergic and Glutamatergic Neurons Derived from the Anterior Hindbrain

Morello, F;Borshagovski, D;Survila, M;Tikker, L;Sadik-Ogli, S;Kirjavainen, A;Estarts, N;Knaapi, L;Lahti, L;Trnen, P;Mazutis, L;Delogu, A;Salminen, M;Achim, K;Partanen, J;

Product: Anti-Cholera Toxin B Subunit (Goat)

  • Stereotaxic surgery and neuronal labeling

    For retrograde tracing, eight week old wild-type ICR mice were used. Mice were anesthetized with isoflurane and attached to the stereotaxic frame. Small hole was drilled into the skull and unilateral, intracranial injections of 300nl of 0.2% Choleratoxin B subunit (CtB; List Biological Lab.Inc. Cat#104) was injected at the speed of 50nl/min using a microinjector (UltraMicroPump III, World Precision Instruments) and microsyringe (Hamilton, Cat#7803-06). Stereotaxic coordinates were measured from bregma in mm. To trace the LDTg neurons, CtB was injected into VTA: −3.1 (AP); 0.36 (ML); −4.65 (DV). Four to six days after the injections mice were intracardially perfused with 4% PFA and brains were collected, thereafter brains were fixed in 4% PFA for 24 h. 100 μm vibratome sections were cut for IHC stainings. Sections were blocked for 1 h in 10% donkey serum in PBS containing 05% Triton X-100 (PBS-T), followed by incubation overnight at room temperature with following antibodies diluted in PBS-T: rabbit anti-Nkx6-1 (1:400, Novus Biologicals); goat anti-CtB (1:5000, List Biologicals #703); mouse anti-TH (1:1000, Merck Millipore) and DAPI. Secondary antibodies conjugated to Alexa 488, 594, or 647 were used for detection. ProLong Gold anti-fade mounting media was used for mounting (Thermo Fisher Scientific, P36930).

    Product #104 – Cholera Toxin B Subunit (Choleragenoid) from Vibrio cholerae in Low Salt
    Product #703 – Anti-Cholera Toxin B Subunit (Goat)

Oligodendrocyte-specific Argonaute profiling identifies microRNAs associated with experimental autoimmune encephalomyelitis

Ma, Q;Matsunaga, A;Ho, B;Oksenberg, JR;Didonna, A;

Product: Pertussis Toxin from B. pertussis, Lyophilized in Buffer

Intranasal mesenchymal stem cell therapy to boost myelination after encephalopathy of prematurity

Vaes, JEG;van Kammen, CM;Trayford, C;van der Toorn, A;Ruhwedel, T;Benders, MJNL;Dijkhuizen, RM;Mbius, W;van Rijt, SH;Nijboer, CH;

Product: Unspecified List Labs LPS

  • 2.2 In vivo mouse model of dWMI

    … After a recovery period of 75 min pups were exposed to 35 min of hypoxia (6% O2) in a temperature‐controlled hypoxic incubator (35.8–36.0°C). Directly following hypoxia, pups were i.p. injected with 1 mg/kg LPS (List Biological Laboratories, Campbell, CA) dissolved in 0.9% NaCl. …

    Author did not specify which List Labs LPS product was utilized in their research.
    List Labs provides the following LPS products: https://listlabs.com/product-information/lipopolysaccharides/