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Merck

RPTMAG-86K

Millipore

MILLIPLEX® Rat Pituitary Magnetic Bead Panel - Endocrine Multiplex Assay

The analytes available for this multiplex kit are: ACTH, BDNF, FSH, GH, LH, Prolactin, TSH.

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About This Item

UNSPSC-Code:
12161503
eCl@ss:
32161000
NACRES:
NA.84

Qualitätsniveau

Speziesreaktivität

rat

Hersteller/Markenname

Milliplex®

assay range

accuracy: 75%
(GH)

accuracy: 88%
(ACTH)

accuracy: 89%
(LH)

accuracy: 90%
(TSH)

sensitivity: 0.38 pg/mL
(BDNF)

sensitivity: 0.87 pg/mL
(TSH)

sensitivity: 1.95 pg/mL
(ACTH)

sensitivity: 3.28 pg/mL
(LH)

sensitivity: 4.64 pg/mL
(Prolactin)

sensitivity: 6.50 pg/mL
(GH)

sensitivity: 7.62 pg/mL
(FSH)

standard curve range: 16-50,000 pg/mL
(GH, Prolactin)

standard curve range: 3.2-10,000 pg/mL
(ACTH, BDNF, LH, TSH)

standard curve range: 32-100,000 pg/mL
(FSH)

inter-assay cv: <20%
intra-assay cv: <10%

Methode(n)

multiplexing: suitable

Nachweisverfahren

fluorometric (Luminex xMAP)

Versandbedingung

wet ice

Allgemeine Beschreibung

Called the “master gland” because it controls many other endocrine glands, the pituitary secretes several key hormones that play important roles in the regulation of metabolism, growth, and reproduction. Piuitary hormones are responsible for the stimulation of the adrenal gland (ACTH), thyroid gland (TSH), ovaries and testes (FSH, LH) and breast milk production (prolactin), as well as blood pressure and the amount of water excreted by the kidneys. Through its connection with the pituitary, the hypothalamus modulates endocrine function by detecting hormone levels. Brain-Derived Neurotrophic Factor (BDNF) is a member of NGF family of neurotrophic factors which are required for differentiation and survival of specific neuronal sub-populations.

MILLIPLEX® Rat Pituitary Panel is a 7-plex kit to be used for the simultaneous quantification of any or all of the following analytes in rat serum or plasma samples, rat tissue extract, or cell/tissue culture supernatant samples: Growth Hormone (GH), Thyroid-Stimulating Hormone (TSH), Adrenocorticotropic Hormone (ACTH), Luteinizing Hormone (LH), Prolactin, Follicle-Stimulating Hormone (FSH), and Brain-Derived Neurotrophic Factor (BDNF). This kit uses a 96-well format, contains a lyophilized standard cocktail, two internal assay quality controls and can measure up to 38 samples in duplicate.

The Luminex® xMAP® platform uses a magnetic bead immunoassay format for ideal speed and sensitivity to quantitate multiple analytes simultaneously, dramatically improving productivity while conserving valuable sample volume.

Panel Type: Endocrine

Anwendung

  • Analytes: Adrenocorticotropic Hormone (ACTH), Brain-Derived Neurotrophic Factor (BDNF), Follicle-Stimulating Hormone (FSH), Growth Hormone (GH), Luteinizing Hormone (LH), Prolactin, Thyroid-Stimulating Hormone (TSH)
  • Recommended Sample Type: Rat serum, plasma, cell/tissue culture supernatants or lysates
  • Recommended Sample Dilution: 25 μL per well 1:3 diluted serum or plasma; cell/tissue culture samples may require dilution in an appropriate control medium.
  • Assay Run Time: Overnight (16-18 hours) at 2-8°C
  • Research Category: Endocrine
  • Research Subcategory: Metabolism

Leistungsmerkmale und Vorteile

Design your multiplex kit by choosing available analytes within this panel.

Rechtliche Hinweise

Luminex is a registered trademark of Luminex Corp
MILLIPLEX is a registered trademark of Merck KGaA, Darmstadt, Germany
xMAP is a registered trademark of Luminex Corp

Piktogramme

Skull and crossbonesEnvironment

Signalwort

Danger

Gefahreneinstufungen

Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Irrit. 2 - Skin Sens. 1

Lagerklassenschlüssel

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects


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Global but not gonadotrope-specific disruption of Bmal1 abolishes the luteinizing hormone surge without affecting ovulation.
Chu, A; Zhu, L; Blum, ID; Mai, O; Leliavski, A; Fahrenkrug, J; Oster, H; Boehm, U; Storch, KF
Endocrinology null
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The obese rodent serves as an indispensable tool for proof-of-concept efficacy and mode-of-action pharmacology studies. Yet the utility of this disease model as an adjunct to the conventional healthy animal in the nonclinical safety evaluation of anti-obesity pharmacotherapies has not

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