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Rat Microtubule-associated protein RP/EB family member 1 (Mapre1) ELISA Kit (RTEB1421)

SKU:
RTEB1421
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
Q66HR2
ELISA Type:
Sandwich
Reactivity:
Rat
€649
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Description

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Rat Microtubule-associated protein RP/EB family member 1 (Mapre1) ELISA Kit

The Rat Microtubule-Associated Protein RP/EB Family Member 1 (MAPRE1) ELISA Kit is a specialized tool for the precise measurement of MAPRE1 levels in rat samples. This kit is highly sensitive and specific, providing accurate and consistent results for research purposes.MAPRE1 is a key protein that plays a role in microtubule dynamics, cell migration, and intracellular transport. It is involved in various cellular processes and is essential for proper cell function.

By measuring MAPRE1 levels, researchers can better understand its function and its implications in diseases such as cancer, neurological disorders, and immune system dysregulation.Overall, the Rat MAPRE1 ELISA Kit is an invaluable resource for studying the role of MAPRE1 in cellular processes and disease pathology, paving the way for potential therapeutic interventions.

Product Name:Rat Microtubule-associated protein RP/EB family member 1 (Mapre1) ELISA Kit
SKU:RTEB1421
Size:96T
Target:Rat Microtubule-associated protein RP/EB family member 1 (Mapre1)
Synonyms:APC-binding protein EB1, End-binding protein 1, EB1
Assay Type:Sandwich
Detection Method:ELISA
Reactivity:Rat
Detection Range:0.156-10ng/mL
Sensitivity:0.091ng/mL
Intra CV:Provided with the Kit
Inter CV:Provided with the Kit
Linearity:Provided with the Kit
Recovery:Provided with the Kit
Function:Binds to the plus end of microtubules and regulates the dynamics of the microtubule cytoskeleton. Promotes cytoplasmic microtubule nucleation and elongation. May be involved in spindle function by stabilizing microtubules and anchoring them at centrosomes. May play a role in cell migration.
Uniprot:Q66HR2
Sample Type:Serum, plasma, tissue homogenates, cell culture supernates and other biological fluids
Specificity:Natural and recombinant rat Microtubule-associated protein RP/EB family member 1
Sub Unit:Homodimer. Heterodimer with MAPRE3. Interacts with DCTN1, DCTN2, DIAPH1, DIAPH2, TERF1 and dynein intermediate chain. Interacts with APC (via C-terminal domain), CLASP2, DST, KIF2C and STIM1; probably required for their targeting to the growing microtubule plus ends. Interacts with MTUS2; interaction is direct and probably targets MTUS2 to microtubules. Interacts with APC2. Interacts with CLASP1 (By similarity). According to PubMed:19553473, MAPRE1 does not interact with CDK5RAP2 (By similarity). Interacts with MACF1. Interacts (via C-terminus) with CLIP1. Interacts with SLAIN (By similarity). Interacts with KIF18B; this interaction is required for efficient accumulation of KIF18B at microtubule plus ends (By similarity). Interacts with MISP (By similarity). Interacts with KCNAB2 (PubMed:21357749) Interacts with RABL2/RABL2A; binds preferentially to GTP-bound RABL2. Interacts with KNSTRN. Interacts with NCKAP5L.
Subcellular Location:Cytoplasm Cytoplasm Cytoskeleton Cytoplasm Cytoskeleton Microtubule organizing center Centrosome Associated with the microtubule network at the growing distal tip of microtubules. Detected along microtubules. Also enriched at the centrosome (By similarity).
Storage:Please see kit components below for exact storage details
Note:For research use only
UniProt Protein Function:EB1: a microtubule-associated protein of the RP/EB family. Binds to the APC protein which is often mutated in familial and sporadic forms of colorectal cancer. Localizes to microtubules, especially the growing ends, in interphase cells. Associates with the centrosomes and spindle microtubules during mitosis. Also associates with components of the dynactin complex and the intermediate chain of cytoplasmic dynein. May be involved in the regulation of microtubule structures and chromosome stability.Protein type: Cytoskeletal; Cell cycle regulation; Microtubule-binding; Motility/polarity/chemotaxisCellular Component: cell projection; cell projection membrane; centrosome; cortical microtubule cytoskeleton; cytoplasm; cytoplasmic microtubule; Golgi apparatus; microtubule; microtubule cytoskeleton; spindleMolecular Function: microtubule binding; microtubule plus-end bindingBiological Process: cell division; mitosis; negative regulation of microtubule polymerization
UniProt Protein Details:
NCBI Summary:expressed specifically at growing microtubule distal tips [RGD, Feb 2006]
UniProt Code:Q66HR2
NCBI GenInfo Identifier:78097100
NCBI Gene ID:114764
NCBI Accession:NP_612518.2
UniProt Secondary Accession:Q66HR2
UniProt Related Accession:Q66HR2
Molecular Weight:30,004 Da
NCBI Full Name:microtubule-associated protein RP/EB family member 1
NCBI Synonym Full Names:microtubule-associated protein, RP/EB family, member 1
NCBI Official Symbol:Mapre1
NCBI Official Synonym Symbols:Eb1
NCBI Protein Information:microtubule-associated protein RP/EB family member 1
UniProt Protein Name:Microtubule-associated protein RP/EB family member 1
UniProt Synonym Protein Names:APC-binding protein EB1; End-binding protein 1; EB1
Protein Family:Microtubule-associated protein RP/EB family
UniProt Gene Name:Mapre1
UniProt Entry Name:MARE1_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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