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Bovine Progesterone(PROG) Elisa Kit

Bovine Progesterone(PROG) Elisa Kit

Bovine Progesterone(PROG) Elisa Kit
Bovine Progesterone(PROG) Elisa Kit

Large Image :  Bovine Progesterone(PROG) Elisa Kit Get Best Price

Product Details:
Place of Origin: CHINA
Brand Name: SPAN
Certification: PROG
Model Number: PROG
Payment & Shipping Terms:
Minimum Order Quantity: 1 KIT
Price: U$300/Kit
Packaging Details: 96T/Box
Delivery Time: within 3-5 working days
Payment Terms: T/T, Western Union,Paypal
Supply Ability: PROG
Detailed Product Description
Specificity: 100%

Intended Use

This kit is used to assay the Progesterone(PROG)in the sample of Bovine ’s serum, blood plasma, and other related tissue Liquid.

 

Test principle

The kit uses a double-antibody sandwich enzyme-linked immunosorbent assay (ELISA) to assay the level of Bovine Progesterone(PROG)in samples. Add Progesterone(PROG) to monoclonal antibody Enzyme well which is pre-coated with Bovine Progesterone(PROG)monoclonal antibody, incubation; then, add Progesterone(PROG)antibodies labeled with biotin, and combined with Streptavidin-HRP to form immune complex; then carry out incubation and washing again to remove the uncombined enzyme. Then add Chromogen Solution A, B, the color of the liquid changes into the blue, And at the effect of acid, the color finally becomes yellow. The chroma of color and the concentration of the Bovine Substance Progesterone(PROG)of sample were positively correlated.

 

Materials supplied in the Test Kit

1 Standard(128ng/ml) 0.5ml 7 Chromogen Solution A 6ml
2 Standard diluent 3ml 8 Chromogen Solution B 6ml
3 Microelisa Stripplate 12w×8s 9 Stop Solution 6ml
4 Str- HRP-Conjugate Reagent 6ml 10 Instruction 1
5 30×wash solution 20ml 11 Closure plate membrane 2
6 Biotin-PROG Ab 1ml 12 Sealed bags 1

 

Materials required but not supplied

1. 37 ℃ incubator 2. Standard Enzyme reader

3. Precision pipettes and Disposable pipette tips 4. Distilled water

5. Disposable tubes for sample dilution 6. Absorbent paper

 

Important Notes

1. Beening taken out from the 2-8℃ environment, the kit should be balanced 30 minutes in the ambient temperature then use. If the Coated plates of Enzyme haven’t been used up after opened, the remaining plates should be stored in Sealed bag.

2. For each step, add Sample with sample injector which should be calibrated frequently, in order to avoid unnecessary experimental tolerance.

3. he operation shall be carried out accordance to the instructions strictly. And test results must be based on the readings of the Enzyme reader.

4. In order to avoid cross-contamination, it is forbidden to re-use the suction head and seal plate membrane in your hands.

5. All samples, washing buffer and each kind of reject should according to infective material process.

6. The idle agents shall be put up or covered. Do not use reagent with different batches. And use them before expired date.

7. The substrate B is light-sensitive. Prolonged exposure to light is forbidden.

 

Washing method

Manually washing method: shake away the remain liquid in the enzyme plates; place some bibulous papers on the test-bed, and flap the plates on the upside down strongly. Inject at least 0.35ml after-dilution washing solution into the well, and marinate 1~2 minutes. Repeat this process according to your requirements.

Automatic washing method: if there is automatic washing machine, it should only be used in the test when you are quite familiar with its function and performance.

 

Precision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Bovine PROG were tested 20 times on one plate, respectively.

Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Bovine PROG were tested on 3 different plates, 8 replicates in each plate.

CV(%) = SD/meanX100

Intra-Assay: CV<10%

Inter-Assay: CV<12%

 

Specimen requirements

1. Can’t detect the sample which contain NaN3, because NaN3 inhibits HRP active.

2. extract as soon as possible after Specimen collection,and according to the relevant literature, and should be experiment as soon as possible after the extraction. If it can’t, specimen can be kept in -20 ℃ to preserve, Avoid repeated freeze-thaw cycles.

3. serum- coagulation at room temperature 10-20 mins,centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again.

4.plasma-use suited EDTA or citrate plasma as an anticoagulant,mix 10-20 mins ,centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again.

5. Urine-collect sue a sterile container, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again. The Operation ofHydrothorax and cerebrospinal fluid Reference to it.

6.cell culture supernatant-detect secretory components, collect sue a sterile container, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant,detect the composition of cells, Dilut cell suspension with PBS(PH7.2-7.4), Cell concentration reached 1 million / ml, repeated freeze-thaw cycles, damage cells and release of intracellular components, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant, If precipitation appeared, Centrifugal again.

7.Tissue samples- After cutting samples, check the weight,add PBS(PH7.2-7.4), Rapidly frozen with liquid nitrogen, maintain samples at 2-8℃ after melting,add PBS(PH7.4), Homogenized by hand or Grinders, centrifugation 20-min at the speed of 2000-3000 r.p.m. remove supernatant.

 

 

 

Rebecca Yan
 
Product Manager
Span Biotech Ltd.
Tel: +86(755)89589611
Cell Phone:+8618823462100(WhatsApp)
Web:www.spanbio.com

 

 

Contact Details
SPAN BIOTECH LTD.

Contact Person: Ms. Anna Lee

Tel: +86-755-89589611

Fax: 86-755-89580096

Send your inquiry directly to us
www.spanbio.com