Rat FADS2 / Fatty acid desaturase 2 ELISA Kit

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SKU:
RTFI00184
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
Q9Z122
Sensitivity:
0.469ng/ml
Range:
0.781-50ng/ml
ELISA Type:
Sandwich ELISA, Double Antibody
Synonyms:
Fads2, FADS2, Fatty acid desaturase 2, D6D, DES6, FADSD6, LLCDL2, SLL0262, TU13
Reactivity:
Rat
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Description

system_update_altデータシートsystem_update_alt安全性データシート
商品名:Rat Fads2 (Fatty acid desaturase 2) ELISA Kit
製品コード:RTFI00184
サイズ:96 Assays
目標:Rat Fads2
エイリアス:Fads2, FADS2, Fatty acid desaturase 2, D6D, DES6, FADSD6, LLCDL2, SLL0262, TU13
反応性:Rat
検出方法:Sandwich ELISA, Double Antibody
感度:0.469ng/ml
範囲:0.781-50ng/ml
保管所:4°C for 6 months
ノート:For Research Use Only
回復:Matrices listed below were spiked with certain level of Rat Fads2 and the recovery rates were calculated by comparing the measured value to the expected amount of Rat Fads2 in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)90-10398
EDTA plasma(n=5)91-10497
UFH plasma(n=5)90-10096
直線性:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat Fads2 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)90-102%86-104%94-101%
EDTA plasma(n=5)84-99%88-97%87-100%
UFH plasma(n=5)80-99%82-94%89-100%
Intra-Assay:CV <8%
Inter-Assay:CV <10%
Uniprot:Q9Z122
UniProt Protein Function:Component of a lipid metabolic pathway that catalyzes biosynthesis of highly unsaturated fatty acids (HUFA) from precursor essential polyunsaturated fatty acids (PUFA) linoleic acid (LA) (18:2n-6) and alpha-linolenic acid (ALA) (18:3n-3). Catalyzes the first and rate limiting step in this pathway which is the desaturation of LA (18:2n-6) and ALA (18:3n-3) into gamma-linoleic acid (GLA) (18:3n-6) and stearidonic acid (18:4n-3) respectively and other desaturation steps. Highly unsaturated fatty acids (HUFA) play pivotal roles in many biological functions.
UniProt Code:Q9Z122
NCBI GenInfo Identifier:13786182
NCBI Gene ID:83512
NCBI Accession:NP_112634.1
UniProt Secondary Accession:Q9Z122,H2BF31,
UniProt Related Accession:Q9Z122
Molecular Weight:52,380 Da
NCBI Full Name:fatty acid desaturase 2
NCBI Synonym Full Names:fatty acid desaturase 2
NCBI Official Symbol:Fads2  
NCBI Official Synonym Symbols:Fadsd6  
NCBI Protein Information:fatty acid desaturase 2
UniProt Protein Name:Fatty acid desaturase 2
UniProt Synonym Protein Names:Delta(6) fatty acid desaturase; D6D; Delta(6) desaturase; Delta-6 desaturase
Protein Family:Fatty acid desaturase
UniProt Gene Name:Fads2  
UniProt Entry Name:FADS2_RAT
ステッププロトコル
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.

ELISAアッセイを実施する場合、可能な限り最良の結果を達成するためにサンプルを準備することが重要です。以下に、さまざまなサンプルタイプのサンプルを準備するための手順のリストを示します。

サンプルタイプ プロトコル
血清

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.

プラズマ 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.
尿および脳脊髄液 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.
細胞培養上清 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.
細胞溶解物 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.
組織ホモジネート 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.
組織溶解物 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.
母乳 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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