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Rat Growth hormone receptor (Ghr) ELISA Kit (RTEB0583)

SKU:
RTEB0583
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P16310
ELISA Type:
Sandwich
Reactivity:
Rat
€649
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Description

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Rat Growth hormone receptor (Ghr) ELISA Kit

The Rat Growth Hormone Receptor (GHR) ELISA Kit is specifically designed for the precise measurement of rat growth hormone receptor levels in biological samples such as serum, plasma, and tissue lysates. With its high sensitivity and specificity, this kit provides accurate and reproducible results, making it an ideal tool for a wide range of research applications.The growth hormone receptor plays a critical role in the regulation of growth and metabolism in the body, making it a key target for studying growth disorders, metabolic diseases, and other related conditions.

By detecting and quantifying the levels of GHR in biological samples, researchers can gain valuable insights into the mechanisms underlying these conditions and potentially develop new therapeutic strategies.Overall, the Rat Growth Hormone Receptor (GHR) ELISA Kit offers a reliable and efficient solution for studying the role of GHR in various physiological and pathological processes, making it a valuable tool for researchers in the field of endocrinology and related disciplines.

Product Name:Rat Growth hormone receptor (Ghr) ELISA Kit
SKU:RTEB0583
Size:96T
Target:Rat Growth hormone receptor (Ghr)
Synonyms:Somatotropin receptor, GH receptor
Assay Type:Sandwich
Detection Method:ELISA
Reactivity:Rat
Detection Range:0.156-10ng/mL
Sensitivity:0.085ng/mL
Intra CV:Provided with the Kit
Inter CV:Provided with the Kit
Linearity:Provided with the Kit
Recovery:Provided with the Kit
Function:The soluble form (GHBP) acts as a reservoir of growth hormone in plasma and may be a modulator/inhibitor of GH signaling.
Uniprot:P16310
Sample Type:Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Specificity:Natural and recombinant rat Growth hormone receptor
Sub Unit:On growth hormone (GH) binding, forms homodimers and binds JAK2 via a box 1-containing domain. Binding to SOCS3 inhibits JAK2 activation, binding to CIS and SOCS2 inhibits STAT5 activation.
Research Area:Cancer
Subcellular Location:Growth hormone-binding protein Secreted Complexed to a substantial fraction of circulating GH.
Storage:Please see kit components below for exact storage details
Note:For research use only
UniProt Protein Function:GH receptor: Receptor for pituitary gland growth hormone involved in regulating postnatal body growth. On ligand binding, couples to the JAK2/STAT5 pathway. Defects in GHR are a cause of Laron syndrome (LARS). A severe form of growth hormone insensitivity characterized by growth impairment, short stature, dysfunctional growth hormone receptor, and failure to generate insulin-like growth factor I in response to growth hormone. Defects in GHR may be a cause of idiopathic short stature autosomal (ISSA). Short stature is defined by a subnormal rate of growth. Belongs to the type I cytokine receptor family. Type 1 subfamily. 4 isoforms of the human protein are produced by alternative splicing.Protein type: Membrane protein, integral; Receptor, cytokineCellular Component: cell soma; cell surface; cytoplasm; extracellular space; extrinsic to membrane; integral to membrane; integral to plasma membrane; mitochondrion; nucleus; plasma membrane; receptor complexMolecular Function: growth factor binding; growth hormone receptor activity; peptide hormone binding; protein homodimerization activity; protein kinase binding; protein phosphatase binding; SH2 domain bindingBiological Process: 2-oxoglutarate metabolic process; activation of JAK protein; activation of MAPK activity; allantoin metabolic process; cellular response to hormone stimulus; cellular response to insulin stimulus; citrate metabolic process; creatine metabolic process; creatinine metabolic process; fatty acid metabolic process; hormone-mediated signaling; insulin-like growth factor receptor signaling pathway; isoleucine metabolic process; JAK-STAT cascade; multicellular organismal metabolic process; oxaloacetate metabolic process; positive regulation of cell differentiation; positive regulation of JAK-STAT cascade; positive regulation of multicellular organism growth; positive regulation of peptidyl-tyrosine phosphorylation; receptor internalization; regulation of multicellular organism growth; response to cycloheximide; response to cytokine stimulus; response to estradiol stimulus; response to food; response to glucocorticoid stimulus; response to hormone stimulus; response to morphine; response to peptide hormone stimulus; succinate metabolic process; taurine metabolic process; tyrosine phosphorylation of JAK2 protein; valine metabolic process
UniProt Protein Details:
NCBI Summary:
UniProt Code:P16310
NCBI GenInfo Identifier:8393434
NCBI Gene ID:25235
NCBI Accession:NP_058790.1
UniProt Secondary Accession:P16310,Q64236, Q80XW9
UniProt Related Accession:P16310
Molecular Weight:31,957 Da
NCBI Full Name:growth hormone receptor
NCBI Synonym Full Names:growth hormone receptor
NCBI Official Symbol:Ghr
NCBI Official Synonym Symbols:GHR/BP
NCBI Protein Information:growth hormone receptor
UniProt Protein Name:Growth hormone receptor
UniProt Synonym Protein Names:Somatotropin receptor
Protein Family:Growth hormone receptor
UniProt Gene Name:Ghr
UniProt Entry Name:GHR_RAT
Component Quantity (96 Assays) Storage
ELISA Microplate (Dismountable) 8×12 strips -20°C
Lyophilized Standard 2 -20°C
Sample Diluent 20ml -20°C
Assay Diluent A 10mL -20°C
Assay Diluent B 10mL -20°C
Detection Reagent A 120µL -20°C
Detection Reagent B 120µL -20°C
Wash Buffer 30mL 4°C
Substrate 10mL 4°C
Stop Solution 10mL 4°C
Plate Sealer 5 -

Other materials and equipment required:

  • Microplate reader with 450 nm wavelength filter
  • Multichannel Pipette, Pipette, microcentrifuge tubes and disposable pipette tips
  • Incubator
  • Deionized or distilled water
  • Absorbent paper
  • Buffer resevoir

*Note: The below protocol is a sample protocol. Protocols are specific to each batch/lot. For the correct instructions please follow the protocol included in your kit.

Allow all reagents to reach room temperature (Please do not dissolve the reagents at 37°C directly). All the reagents should be mixed thoroughly by gently swirling before pipetting. Avoid foaming. Keep appropriate numbers of strips for 1 experiment and remove extra strips from microtiter plate. Removed strips should be resealed and stored at -20°C until the kits expiry date. Prepare all reagents, working standards and samples as directed in the previous sections. Please predict the concentration before assaying. If values for these are not within the range of the standard curve, users must determine the optimal sample dilutions for their experiments. We recommend running all samples in duplicate.

Step
1. Add Sample: Add 100µL of Standard, Blank, or Sample per well. The blank well is added with Sample diluent. Solutions are added to the bottom of micro ELISA plate well, avoid inside wall touching and foaming as possible. Mix it gently. Cover the plate with sealer we provided. Incubate for 120 minutes at 37°C.
2. Remove the liquid from each well, don't wash. Add 100µL of Detection Reagent A working solution to each well. Cover with the Plate sealer. Gently tap the plate to ensure thorough mixing. Incubate for 1 hour at 37°C. Note: if Detection Reagent A appears cloudy warm to room temperature until solution is uniform.
3. Aspirate each well and wash, repeating the process three times. Wash by filling each well with Wash Buffer (approximately 400µL) (a squirt bottle, multi-channel pipette,manifold dispenser or automated washer are needed). Complete removal of liquid at each step is essential. After the last wash, completely remove remaining Wash Buffer by aspirating or decanting. Invert the plate and pat it against thick clean absorbent paper.
4. Add 100µL of Detection Reagent B working solution to each well. Cover with the Plate sealer. Incubate for 60 minutes at 37°C.
5. Repeat the wash process for five times as conducted in step 3.
6. Add 90µL of Substrate Solution to each well. Cover with a new Plate sealer and incubate for 10-20 minutes at 37°C. Protect the plate from light. The reaction time can be shortened or extended according to the actual color change, but this should not exceed more than 30 minutes. When apparent gradient appears in standard wells, user should terminatethe reaction.
7. Add 50µL of Stop Solution to each well. If color change does not appear uniform, gently tap the plate to ensure thorough mixing.
8. Determine the optical density (OD value) of each well at once, using a micro-plate reader set to 450 nm. User should open the micro-plate reader in advance, preheat the instrument, and set the testing parameters.
9. After experiment, store all reagents according to the specified storage temperature respectively until their expiry.

When carrying out an ELISA assay it is important to prepare your samples in order to achieve the best possible results. Below we have a list of procedures for the preparation of samples for different sample types.

Sample Type Protocol
Serum If using serum separator tubes, allow samples to clot for 30 minutes at room temperature. Centrifuge for 10 minutes at 1,000x g. Collect the serum fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. If serum separator tubes are not being used, allow samples to clot overnight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Remove serum and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles.
Plasma Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples at 4°C for 15 mins at 1000 × g within 30 mins of collection. Collect the plasma fraction and assay promptly or aliquot and store the samples at -80°C. Avoid multiple freeze-thaw cycles. Note: Over haemolysed samples are not suitable for use with this kit.
Urine & Cerebrospinal Fluid Collect the urine (mid-stream) in a sterile container, centrifuge for 20 mins at 2000-3000 rpm. Remove supernatant and assay immediately. If any precipitation is detected, repeat the centrifugation step. A similar protocol can be used for cerebrospinal fluid.
Cell culture supernatant Collect the cell culture media by pipette, followed by centrifugation at 4°C for 20 mins at 1500 rpm. Collect the clear supernatant and assay immediately.
Cell lysates Solubilize cells in lysis buffer and allow to sit on ice for 30 minutes. Centrifuge tubes at 14,000 x g for 5 minutes to remove insoluble material. Aliquot the supernatant into a new tube and discard the remaining whole cell extract. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.
Tissue homogenates The preparation of tissue homogenates will vary depending upon tissue type. Rinse tissue with 1X PBS to remove excess blood & homogenize in 20ml of 1X PBS (including protease inhibitors) and store overnight at ≤ -20°C. Two freeze-thaw cycles are required to break the cell membranes. To further disrupt the cell membranes you can sonicate the samples. Centrifuge homogenates for 5 mins at 5000xg. Remove the supernatant and assay immediately or aliquot and store at -20°C or -80°C.
Tissue lysates Rinse tissue with PBS, cut into 1-2 mm pieces, and homogenize with a tissue homogenizer in PBS. Add an equal volume of RIPA buffer containing protease inhibitors and lyse tissues at room temperature for 30 minutes with gentle agitation. Centrifuge to remove debris. Quantify total protein concentration using a total protein assay. Assay immediately or aliquot and store at ≤ -20 °C.
Breast Milk Collect milk samples and centrifuge at 10,000 x g for 60 min at 4°C. Aliquot the supernatant and assay. For long term use, store samples at -80°C. Minimize freeze/thaw cycles.

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