Rat Pfkm / 6-phosphofructokinase ELISA Kit

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SKU:
RTFI00235
Product Type:
ELISA Kit
Size:
96 Assays
Uniprot:
P47858
Sensitivity:
0.188ng/ml
Range:
0.313-20ng/ml
ELISA Type:
Sandwich ELISA, Double Antibody
Synonyms:
Pfkm, GSD7, PFK-1, PFK-A, PFKM, PFKX, Phosphofructokinase-1, Phosphofructokinase-M, Phosphohexokinase, 6-phosphofructokinase, muscle type, EC 2.7.1, 6-phosphofructo-1-kinase, EC 2.7.1.11, GSD7, MGC8699, PFK1, PFKA, PFK-A, PFKX, Phosphofructo-1-kinase
Reactivity:
Rat
Frequently bought together:

Description

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Product Name:Rat Pfkm (6-phosphofructokinase, muscle type) ELISA Kit
Product Code:RTFI00235
Size:96 Assays
Target:Rat Pfkm
Alias:Pfkm, GSD7, PFK-1, PFK-A, PFKM, PFKX, Phosphofructokinase-1, Phosphofructokinase-M, Phosphohexokinase, 6-phosphofructokinase, muscle type, EC 2.7.1, 6-phosphofructo-1-kinase, EC 2.7.1.11, GSD7, MGC8699, PFK1, PFKA, PFK-A, PFKX, Phosphofructo-1-kinase isozyme A, Phosphofructokinase 1, phosphofructokinase, muscle, phosphofructokinase, polypeptide X, phosphofructokinase-M, Phosphofructokinase-M, phosphohexokinase, Phosphohexokinase
Reactivity:Rat
Detection Method:Sandwich ELISA, Double Antibody
Sensitivity:0.188ng/ml
Range:0.313-20ng/ml
Storage:4°C for 6 months
Note:For Research Use Only
Recovery:Matrices listed below were spiked with certain level of Rat Pfkm and the recovery rates were calculated by comparing the measured value to the expected amount of Rat Pfkm in samples.
MatrixRecovery range(%)Average(%)
serum(n=5)87-10396
EDTA plasma(n=5)90-10497
UFH plasma(n=5)90-10497
Linearity:The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Rat Pfkm and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
Sample1:21:41:8
serum(n=5)88-102%86-96%90-101%
EDTA plasma(n=5)82-98%83-98%83-101%
UFH plasma(n=5)83-95%80-100%88-97%
Intra-Assay:CV <8%
Inter-Assay:CV <10%
Uniprot:P47858
UniProt Protein Function:PFKM: phosphofructokinase, muscle type. An ubiquitous metabolic enzyme involved in the synthesis and degradation of fructose 2,6-bisphosphate. Key control step of glycolysis. An allosteric enzyme activated by ADP, AMP, or fructose bisphosphate and inhibited by ATP or citrate. Activity: ATP D-fructose 6-phosphate = ADP D-fructose 1,6-bisphosphate. The holoenzyme consists of 4 subunits. The liver and muscle enzymes are homo-tetramers of four liver or muscle isoforms, respectively. The red blood cell enzyme consists hetero-tetramers of the muscle and liver isoforms. A subunit composition with a higher proportion of platelet type subunits is found in platelets, brain and fibroblasts. Defects in PFKM are the cause of glycogen storage disease VII (GSD-VII) also known as Tarui disease. Two alternatively spliced isoforms have been described.
UniProt Protein Details:

Protein type:Carbohydrate Metabolism - galactose; Carbohydrate Metabolism - glycolysis and gluconeogenesis; Carbohydrate Metabolism - fructose and mannose; Kinase, other; EC 2.7.1.11; Carbohydrate Metabolism - pentose phosphate pathway

Cellular Component: 6-phosphofructokinase complex; apical plasma membrane; cytoplasm; cytosol

Molecular Function:6-phosphofructokinase activity; AMP binding; ATP binding; carbohydrate binding; identical protein binding; kinase binding; metal ion binding; phosphofructokinase activity; protein C-terminus binding; protein homodimerization activity

Biological Process: carbohydrate phosphorylation; cell glucose homeostasis; fructose 1,6-bisphosphate metabolic process; fructose 6-phosphate metabolic process; glucose homeostasis; glycogen catabolic process; glycolysis; muscle maintenance; positive regulation of insulin secretion; protein homotetramerization; protein oligomerization

NCBI Summary:phosphofructokinase isozyme A; may regulate glycolytic flux and influence insulin secretion [RGD, Feb 2006]
UniProt Code:P47858
NCBI GenInfo Identifier:13929002
NCBI Gene ID:65152
NCBI Accession:NP_113903.1
UniProt Secondary Accession:P47858,Q63736,
UniProt Related Accession:P47858
Molecular Weight:85,560 Da
NCBI Full Name:ATP-dependent 6-phosphofructokinase, muscle type
NCBI Synonym Full Names:phosphofructokinase, muscle
NCBI Official Symbol:Pfkm  
NCBI Official Synonym Symbols:PFK-A; Pfk-M; ATP-PFK  
NCBI Protein Information:ATP-dependent 6-phosphofructokinase, muscle type
UniProt Protein Name:ATP-dependent 6-phosphofructokinase, muscle type
UniProt Synonym Protein Names:6-phosphofructokinase type A; Phosphofructo-1-kinase isozyme A; PFK-A; Phosphohexokinase
Protein Family:ATP-dependent 6-phosphofructokinase
UniProt Gene Name:Pfkm  
UniProt Entry Name:PFKAM_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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