7
What did the customer think? Antibody Specificity: Antibody RPPA Rating: Testing results were provided independently by J. Huang at Newcastle University. They stated “A unique assumed Puma protein band was detected at the position of 30KD (in red) and is higher than the suggested 23KD from provided data sheet by anti-Puma (STJ95272) antibody with 1:500 dilutions and a rabbit Alexa fluor 680 secondary antibody. An actin band is also illustrated in green at 46KD using the actin antibody from Abcam (ab6276) and the mouse Dylight 800 conjugated secondary antibody.” 46 32 57 76 100 22 17 25 Actin Puma (KD)

Western Blot Antibody Customer Review for Anti-PUMA Polyclonal Antibody (STJ95272)

Embed Size (px)

Citation preview

Page 1: Western Blot Antibody Customer Review for Anti-PUMA Polyclonal Antibody (STJ95272)

What did the customer think?Antibody Specificity:

Antibody RPPA Rating:

Testing results were provided independently by J. Huang at Newcastle University. They stated “A unique assumed Puma protein band was detected at the position of 30KD (in red) and is higher than the suggested 23KD from provided data sheet by anti-Puma (STJ95272) antibody with 1:500 dilutions and a rabbit Alexa fluor 680 secondary antibody. An actin band is also illustrated in green at 46KD using the actin antibody from Abcam (ab6276) and the mouse Dylight 800 conjugated secondary antibody.”

46

32

57

76

100

2217

25

Actin

Puma

(KD)

Page 2: Western Blot Antibody Customer Review for Anti-PUMA Polyclonal Antibody (STJ95272)

What was used?Primary antibody: STJ95272 anti-PUMA Antibody

Provider: St John's Laboratory Ltd.

Dilution ratio: 1:500

Application: Western Blot

Materials for validation: Lysates from Hela cell line

Click for product data sheet PDF

Page 3: Western Blot Antibody Customer Review for Anti-PUMA Polyclonal Antibody (STJ95272)

What Was The Protocol?Treatment of Materials When cells were cultured to 70%-80% plating density, lysis buffer with protease inhibitors

(Sigma) and equal volume of 2X loading buffer were added and heated at 100˚C for 10 minutes. Supernatant was collected after centrifugation at 12,000 rpm for 25 minutes at 4°C and used for 10% Bis-Tris plus gel for protein separation.

Gel Electrophoresis 10% polyacrylamide gel, constant voltage 160 V, 60 minutes.

Transfer 0.45 µm PVDF membrane, 1 piece of gel (wet transfer), constant current 80 Amp for 90 minutes.

Blocking 1X Odyssey blocking solution for 2 hours at RT

Primary Antibody Probing Primary antibody was added to the 1X Odyssey blocking solution with 1:500 dilution, and the membrane was incubated at 4˚C overnight with agitation.

Membrane Wash 1X TBST wash 3 times

Secondary Antibody Probing Secondary antibody was added to 1X Odyssey blocking solution with 1:1000 dilution ratio, for 1.5 hours at RT

Membrane Wash 1X TBST wash 3 times

Visualization Fluorescent signals were visualized using a Li-Cor Odyseey machine using 700nm and 800nm detecting channels

Page 4: Western Blot Antibody Customer Review for Anti-PUMA Polyclonal Antibody (STJ95272)

What was the protocol?10% polyacrylamide gel, constant voltage 160 V, 60 minutes.

0.45 µm PVDF membrane, 1 piece of gel (wet transfer), constant current 80 Amp for 90 minutes.

No. Antigen Loading amount

Primary antibody

Primary antibody

dilution ratio

Secondaryantibody

dilution ratioTarget band KD Visualization

time

1 Hela lysate 10µg (total protein)

STJ95272 anti-PUMA Antibody

1:500 1:0000 ~23KD N/A

2 ~46KD N/A1:0000Actin-beta 1:1000

Page 6: Western Blot Antibody Customer Review for Anti-PUMA Polyclonal Antibody (STJ95272)

1. Order any STJ9 catalogued product using this online form.

2. Test it in your laboratory using your preferred method.

3. Return a fully completed review form to receive rewards.

…in 3 simple steps…

Page 7: Western Blot Antibody Customer Review for Anti-PUMA Polyclonal Antibody (STJ95272)

@StJohnsLabs

http://www.slideshare.net/stjohnslabs