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Rat CA2 (Carbonic Anhydrase 2) ELISA Kit (RTFI00622)

SKU:
RTFI00622
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P27139
Sensitivity:
0.094ng/ml
Range:
0.156-10ng/ml
ELISA Type:
Sandwich
Synonyms:
CA2, Carbonic Anhydrase II, Carbonic anhydrase 2, CA-II, Carbonic anhydrase C, CAC
Reactivity:
Rat
€649
Frequently bought together:

Description

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Rat CA2 (Carbonic Anhydrase 2) ELISA Kit

The Rat CA2 (Carbonic Anhydrase 2) ELISA Kit is specifically designed for the accurate quantification of CA2 levels in rat serum, plasma, and cell culture supernatants. With its high sensitivity and specificity, this kit delivers reliable and reproducible results, making it an invaluable tool for a variety of research applications.Carbonic anhydrase 2 is an enzyme that plays a critical role in regulating pH balance in the body and is involved in numerous physiological processes.

Dysregulation of CA2 has been linked to various diseases and conditions, making it a valuable biomarker for studying these disorders and potentially developing targeted therapies.Overall, the Rat CA2 ELISA Kit offers researchers a powerful tool for studying the role of carbonic anhydrase 2 in disease progression and identifying potential therapeutic targets.

Product Name:Rat CA2 (Carbonic Anhydrase II) ELISA Kit
Product Code:RTFI00622
Size:96 Assays
Target:Rat CA2
Alias:CA2, Carbonic Anhydrase II, Carbonic anhydrase 2, CA-II, Carbonic anhydrase C, CAC
Reactivity:Rat
Detection Method:Sandwich ELISA, Double Antibody
Sensitivity:0.094ng/ml
Range:0.156-10ng/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery:Matrices listed below were spiked with certain level of Rat CA2 and the recovery rates were calculated by comparing the measured value to the expected amount of Rat CA2 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)87-10096
EDTA plasma(n=5)93-10598
UFH plasma(n=5)86-10594
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat CA2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)88-104%88-101%86-104%
EDTA plasma(n=5)83-97%92-101%83-98%
UFH plasma(n=5)90-99%80-99%83-98%
Intra-Assay:CV <8%
Inter-Assay:CV <10%
Uniprot:P27139
UniProt Protein Function:CA2: Essential for bone resorption and osteoclast differentiation. Reversible hydration of carbon dioxide. Can hydrates cyanamide to urea. Involved in the regulation of fluid secretion into the anterior chamber of the eye. Interacts with SLC4A4. Interaction with SLC4A7 regulates SLC4A7 transporter activity. Activated by X-ray, histamine, L-adrenaline, L- and D-phenylalanine, L- and D-histidine, L-His-OMe and beta-Ala- His (carnosine). Competitively inhibited by saccharin, thioxolone, coumarins, 667-coumate, celecoxib (Celebrex), valdecoxib (Bextra), SC-125, SC-560, diclofenac, acetate, azide, bromide, sulfonamide derivatives such as acetazolamide (AZA), methazolamide (MZA), ethoxzolamide (EZA), dichlorophenamide (DCP), brinzolamide, dansylamide, thiabendazole-5-sulfonamide, trifluoromethane sulfonamide and N-hydroxysulfamide, fructose-based sugar sulfamate RWJ-37497, and Foscarnet (phosphonoformate trisodium salt). Repressed strongly by hydrogen sulfide(HS) and weakly by nitrate (NO(3)). Esterase activity weakly reduced by cyanamide. N- hydroxyurea interfers with zinc binding and inhibit activity. Belongs to the alpha-carbonic anhydrase family.
UniProt Protein Details:

Protein type:Energy Metabolism - nitrogen; EC 4.2.1.1; Lyase

Cellular Component: apical part of cell; axon; basolateral plasma membrane; cytoplasm; cytosol; extracellular space; microvillus; myelin sheath; plasma membrane

Molecular Function:arylesterase activity; carbonate dehydratase activity; protein binding; zinc ion binding

Biological Process: carbon dioxide transport; kidney development; morphogenesis of an epithelium; odontogenesis of dentine-containing teeth; one-carbon compound metabolic process; osteoclast differentiation; positive regulation of bone resorption; positive regulation of cellular pH reduction; positive regulation of osteoclast differentiation; positive regulation of synaptic transmission, GABAergic; regulation of bone resorption; regulation of cellular pH; regulation of intracellular pH; response to estrogen stimulus; response to organic substance; response to pH; response to steroid hormone stimulus; response to zinc ion; secretion

NCBI Summary:putative carbonic anhydrase; human homolog catalyzes the reversible hydration of carbon dioxide [RGD, Feb 2006]
UniProt Code:P27139
NCBI GenInfo Identifier:9506445
NCBI Gene ID:54231
NCBI Accession:NP_062164.1
UniProt Related Accession:P27139
Molecular Weight:29,114 Da
NCBI Full Name:carbonic anhydrase 2
NCBI Synonym Full Names:carbonic anhydrase 2
NCBI Official Symbol:Car2  
NCBI Official Synonym Symbols:Ca2  
NCBI Protein Information:carbonic anhydrase 2
UniProt Protein Name:Carbonic anhydrase 2
UniProt Synonym Protein Names:Carbonate dehydratase II; Carbonic anhydrase II; CA-II
Protein Family:Carbonic anhydrase
UniProt Gene Name:Ca2  
UniProt Entry Name:CAH2_RAT
StepProcedure
1. Set standard, test sample and control (zero) wells on the pre-coated plate respectively, and then, record their positions. It is recommended to measure each standard and sample in duplicate. Wash plate 2 times before adding standard, sample and control (zero) wells!
2.Aliquot 0.1ml standard solutions into the standard wells.
3. Add 0.1 ml of Sample / Standard dilution buffer into the control (zero) well.
4. Add 0.1 ml of properly diluted sample ( Human serum, plasma, tissue homogenates and other biological fluids.) into test sample wells.
5.Seal the plate with a cover and incubate at 37°C for 90 min.
6. Remove the cover and discard the plate content, clap the plate on the absorbent filter papers or other absorbent material. Do NOT let the wells completely dry at any time. Wash plate X2.
7. Add 0.1 ml of Biotin- detection antibody working solution into the above wells (standard, test sample & zero wells). Add the solution at the bottom of each well without touching the side wall.
8.Seal the plate with a cover and incubate at 37°C for 60 min.
9. Remove the cover, and wash plate 3 times with Wash buffer. Let wash buffer rest in wells for 1 min between each wash.
10. Add 0.1 ml of SABC working solution into each well, cover the plate and incubate at 37°C for 30 min.
11. Remove the cover and wash plate 5 times with Wash buffer, and each time let the wash buffer stay in the wells for 1-2 min.
12. Add 90 µL of TMB substrate into each well, cover the plate and incubate at 37°C in dark within 10-20 min. (Note: This incubation time is for reference use only, the optimal time should be determined by end user.) And the shades of blue can be seen in the first 3-4 wells (with most concentrated standard solutions), the other wells show no obvious color.
13. Add 50 µL of Stop solution into each well and mix thoroughly. The color changes into yellow immediately.
14. Read the O.D. absorbance at 450 nm in a microplate reader immediately after adding the stop solution.

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 clotovernight at 2-8°C. Centrifuge for 10 minutes at 1,000x g. Removeserum 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 anti-coagulant. 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 & homogenizein 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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