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  • Immunofluorescence analysis of paraformaldehyde fixed HeLa cells,  permeabilized with 0.15% Triton. Primary incubation 1hr (1:100 dilution) followed by Alexa Fluor® 488 secondary antibody (1:1000 dilution), showing cytoplasmic and nuclear staining. The nuclear stain is DAPI (blue). Negative control: Mouse IgG1 negative control followed by Alexa Fluor® 488 secondary antibody.
  • (0.1µg/ml) staining in K562 cells lysate (35µg protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
  • HeLa lysate run on 4-12% Bis-Tris 2D gel in 1 x MOPS running buffer. Transfer to 0.45µm nitrocellulose. Membrane probed with 10E10 (anti-PABP). Anti-mouse IgG (whole molecule)-AP conjugate (1 in 2,000). Detection with BCIP/NBT substrate.

Current Image Legend:




PABP Monoclonal Antibody [10E10]

Catalogue Number: IQ216

Catalogue Number: IQ272

Catalogue Number: IQ216AF

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  • £328.90

Datasheet

Download Variant Datasheet
Primary Description: Mouse Anti-PABP [10E10]
Primary Description: PABP Antibody [10E10]
Primary Description: Mouse Anti-PABP [10E10]- BSA/Azide Free
Target Antigen: PABP
Target Antigen: PABP
Target Antigen: PABP
Catalogue Number: IQ216
Catalogue Number: IQ272
Catalogue Number: IQ216AF
Quantity: 0.1mg
Quantity: 0.05mg
Quantity: 0.05mg
Concentration: 1mg/ml
Concentration: 1mg/ml
Concentration: 1mg/ml
Clone: 10E10
Clone: 10E10
Clone: 10E10
Host: Mouse
Host: Mouse 
Host: Mouse
Isotype: IgG2b
Isotype: IgG2b
Isotype: IgG2b
Myeloma/Fusion Partners: SP2/0
Myeloma/Fusion Partners: SP2/0
Myeloma/Fusion Partners: Sp2/0
Immunogen: Recombinant PABP (Human) expressed from its 1.85 kbp cDNA, NcoI to SspI
Immunogen: Recombinant PABP (Human) expressed from its 1.85 kbp cDNA, NcoI to SspI
Immunogen: Recombinant PABP (Human) expressed from its 1.85 kbp cDNA, NcoI to SspI
Species Reactivity: Rabbit, Chicken, Human, Xenopus laevis, Hamster
Species Reactivity: Rabbit, Chicken, Human, Xenopus laevis, Hamster
Species Reactivity: Rabbit, Chicken, Human, Xenopus laevis, Hamster
Purification: Protein G
Purification: Protein G
Purification: Protein G
Format: Purified antibody (from supernatant) containing PBS + 0.1% sodium azide;
Format: Purified antibody (from supernatant) containing PBS + 0.1% sodium azide;
Format: Purified antibody (from supernatant) containing PBS. Does not contain sodium azide or BSA
Applications: ELISA, WB, IP, ICC/IF, Flow Cyt
Applications: ELISA, WB, IP, ICC/IF, Flow Cyt
Applications: ELISA, WB, IP, ICC/IF, Flow Cyt
Dilutions: Optimal antibody dilution should be determined by titration, however try:WB: Use at an assay dependent dilution. Detects a band of approximately 70 kDa (predicted molecular weight: 71 kDa)ICC/IF: Use at an assay dependent dilution. PubMed: 17977970Flow Cyt: Use 1µg for 106 cells
Dilutions: Optimal antibody dilution should be determined by titration, however try:WB: Use at an assay dependent dilution. Detects a band of approximately 70 kDa (predicted molecular weight: 71 kDa)ICC/IF: Use at an assay dependent dilution. PubMed: 17977970Flow Cyt: Use 1µg for 106 cells
Dilutions: Optimal antibody dilution should be determined by titration, however try:WB: Use at an assay dependent dilution. Detects a band of approximately 70 kDa (predicted molecular weight: 71 kDa)ICC/IF: Use at an assay dependent dilution. PubMed: 17977970Flow Cyt: Use 1µg for 106 cells
Pubmed ID(s): 22577345, 21518916, 20547756, 20453113, 18296717, 16716377, 16714065, 16407409, 16221671
Pubmed ID(s): 22577345, 21518916, 20547756, 20453113, 18296717, 16716377, 16714065, 16407409, 16221671
Pubmed ID(s): x22577345, 21518916, 20547756, 20453113, 18296717, 16716377, 16714065, 16407409, 16221671
Entrez Gene ID(s): 26986
Entrez Gene ID(s): 26986
Entrez Gene ID(s): 26986
SwissProt ID(s): P11940
SwissProt ID(s): P11940
SwissProt ID(s): P11940

Citations

Citation Count: 9
Citations:

Briggs JW  et al. The ezrin metastatic phenotype is associated with the initiation of protein translation. Neoplasia 14:297-310 (2012)
View Source


Gorgoni B  et al. Poly(A)-binding proteins are functionally distinct and have essential roles during vertebrate development. Proc Natl Acad Sci U S A 108:7844-9 (2011)
View Source


Rattenbacher B et al. Analysis of CUGBP1 targets identifies GU-repeat sequences that mediate rapid mRNA decay. Mol Cell Biol. 2010 Aug;30(16):3970-80. doi: 10.1128/MCB.00624-10. Epub 2010 Jun 14.  IP ; Human
View Source


Unsworth H  et al. mRNA escape from stress granule sequestration is dictated by localization to the endoplasmic reticulum. FASEB J 24:3370-80 (2010)
View Source


Kanno T et al. Expression of Kaposi's sarcoma-associated herpesvirus-encoded K10/10.1 protein in tissues and its interaction with poly(A)-binding protein. Virology. 2006 Aug 15;352(1):100-9. Epub 2006 May 22.  ICC/IF IP WB ; Human
View Source


Nagaoka K et al. Stability of casein mRNA is ensured by structural interactions between the 3'-untranslated region and poly(A) tail via the HuR and poly(A)-binding protein complex. Biochim Biophys Acta. 2006 Mar-Apr;1759(3-4):132-40. Epub 2006 Apr 20.  WB ; Rabbit
View Source


Hofmann I et al. Identification of the junctional plaque protein plakophilin 3 in cytoplasmic particles containing RNA-binding proteins and the recruitment of plakophilins 1 and 3 to stress granules. Mol Biol Cell. 2006 Mar;17(3):1388-98. Epub 2006 Jan 11. ICC/IF WB IP ; Human
View Source


Baez MV et al. Mammalian Smaug is a translational repressor that forms cytoplasmic foci similar to stress granules. J Biol Chem. 2005 Dec 30;280(52):43131-40. Epub 2005 Oct 12.  ICC/IF ; Hamster
View Source


The mRNA poly(A)binding protein: localization, abundance, and RNAbinding specificity. Grlach M ( Exp Cell Res.,April 1994) 
View Source


Protocols

Immunofluorescence protocol - Formaldehyde fixation
  1. Collect cells from T.c.unit and remove media from petri dish using suction.
  2. Wash with 1x PBS and remove.
  3. Incubate cells in pre-warm (37°C) Para-Formaldehyde for 12 minutes at room temperature on an orbital shaker.
  4. Remove PFA and incubate in 0.5% Triton X-IOO in 1x PBS for 5 minutes at room temperature.
  5. Prepare blocking reagent, this is also the antibody diluent.
  6. Wash cells 2x with 1x PBS at room temperature, for 4 minutes/wash on an orbital shaker.
  7. Block with 1 % NCS and 1x PBS for 30 minutes at room temperature.
  8. Prepare primary antibodies (50?l/coverslip) and moist staining chambers.
  9. Wash cells 2x with lx PBS at room temperature and air dry briefly.
  10. Incubate with primary antibody for 1 hr at room temperature in the dark in staining chambers. During this time prepare the secondary antibody.
  11. Wash cells 5x with 1x PBS (5 beaker changes/5 counts in each beaker)
  12. Incubate with secondary antibody for 1 hour at room temperature in the dark in staining chambers.
  13. Wash cells 5x with 1x PBS.
  14. Mount in Dapi.

Solutions (prepare fresh the same day of staining).

  • * 1x Phosphate buffered saline.
  • * Blocking reagent: 1% NCS in 1x PBS (use fresh l0x PBS).
  • * Fixation solution: 3.5% Para formaldehyde.

1.75g PFA in 20 ml d.H20 plus 5 drops 1M NaOH. Stir on a hot plate at 50-60°C until dissolved. Add 4 drops IN HCI and check pH indicator strip. PH should be 7.4. Complete volume with d.H20 to 25ml and add 25ml 2xPBS. Check pH before adding to cover slips.

Immunofluorescence protocol - Methanol/acetone fixation
  1. Collect cells from T.C.unit and remove media from petri dish using suction.
  2. Wash with 1x PBS and remove.
  3. Fix cells with cold methanol: acetone 1: 1 for 10 minutes on ice.
  4. Prepare blocking reagent, this is also the diluent for the antibodies.
  5. Remove fixative and wash cells 3x with Ix PBS at RT, for 4 minutes/wash on orbital shaker.
  6. Block with 1% NCS and Ix PBS for 30 minutes at RT.
  7. Prepare primary antibodies (50?l/coverslip) and moist staining chambers.
  8. Wash cells 2x with 1 x PBS at RT and air dry for approximately 7 minutes.
  9. Incubate with primary antibody for 1 hr at RT in the dark in staining chambers. During this time prepare secondary antibody.
  10. Wash cells 5x with 1x PBS (5 beaker changes/5 counts in each beaker)
  11. Incubate with secondary antibody for 1 hr at R T in the dark in staining chambers.
  12. Wash cells 5x with 1x PBS.
  13. Mount in Dapi.

Solutions (prepare fresh the same day of staining)

  • * 1x Phosphate buffered saline.
  • * Blocking reagent: 1% NCS in 1x PBS (use fresh 10x PBS).
  • * Fixation solution: methanol:acetone 1: 1 ice cold.
Western Blotting Protocol
  1. Transfer gel to PDVF or nitrocellulose membrane
  2. Place membrane in plastic tray in blocking buffer for one hour with agitation
  3. Rinse in wash buffer
  4. Incubate in wash buffer plus primary antibody for one hour
  5. Wash 6 X 5 minutes with wash buffer
  6. Incubate in wash buffer plus secondary antibody for one hour
  7. Wash 6X 5 minutes with wash buffer
  8. Detect (e.g. ECL, Amersham according to manufacturers instructions)
Wash buffer

PBS + 0.1% Tween 20

Blocking buffer

Wash buffer + 5% dried milk powder

The concentration of antibodies used depends on each antibody, the amount of antigen and the detection method used. Generally, dilution is in the range of a few hundred times dilution to a few thousand times dilution, but usually has to be determined empirically.

FAQ's

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Formal acceptance of an order will take place when the goods are dispatched. If prices should be changed between the time of receipt of an order and dispatch, ImmuQuest will contact you in advance.

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If items are ordered incorrectly by the customer, ImmuQuest will consider taking them back as long as they have been stored correctly and have not been opened or tampered with. Such orders may be subject to a 15% restocking charge on the items plus any shipping costs.

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We use federal Express for UK & international shipments, andfor standard shipments the cost is £30 UK & £55 international. If the customer uses their account, we charge a £20 handling fee (UK & international)

We are strongly committed to providing the best quality products, and the best service possible.

Should any product not perform as described in the product literature, it will be replaced or a full refund will be given. The customer must notify ImmuQuest within 30 days after the goods have been received to request a replacement, forwarding complete test data as requested by ImmuQuest.

If items are ordered incorrectly by the customer, ImmuQuest will consider taking them back as long as they have been stored correctly and have not been opened or tampered with. Such orders may be subject to a 15% restocking charge on the items plus any shipping costs.

Requests for returns must have prior authorization from ImmuQuest, and must be made within 7 days of receipt of the items. Items must be returned in the same or equivalent packaging as originally dispatched, and by an equivalent method of delivery.

Product Guarantee

We are strongly committed to providing the best quality products, and the best service possible. In order to do this we depend on your feedback.

Should any product not perform as described in the product literature, it will be replaced or a full refund will be given. The customer must notify ImmuQuest within 30 days after the goods have been received to request a replacement, forwarding complete test data as requested by ImmuQuest.

If items are ordered incorrectly by the customer, ImmuQuest will consider taking them back as long as they have been stored correctly and have not been opened or tampered with. Such orders may be subject to a 15% restocking charge on the items plus any shipping costs.

Requests for returns must have prior authorization from ImmuQuest, and must be made within 7 days of receipt of the items. Items must be returned in the same or equivalent packaging as originally dispatched, and by an equivalent method of delivery.

If you have any questions please contact us using the following details:

ImmuQuest Ltd
Springboard
Stokesley Business Park
24 Ellerbeck Way
Stokesley
TS9 5JZ
UK

Tel: 01642 713533
Fax: 01642 713988
International Tel: +44 1642 713533
International Fax: +44 1642 713988

When placing an order ImmuQuest require a purchase order number, plus name and contact details of the purchaser, and the person who will be using the product. ImmuQuest will also need a VAT number for customers in the European Union.UK customers that are VAT exempt need to fax an exemption certificate.

Orders can be placed either by our website, via email or by mail. Please see our contact us page for more details. All orders are subject to availability. Prices of products do not include shipping, VAT or import duties where these are applicable.

Price and other information provided are subject to change without notice. While every effort is made to keep information provided Up to date, ImmuQuest will not be liable if errors should occur in such information. Formal acceptance of an order will take place when the goods are dispatched. If prices should be changed between the time of receipt of an order and dispatch, ImmuQuest will contact you in advance.