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Application Data (Overlay histogram showing Hela cells stained with AAA18857 (red line). The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min. The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (10ug/1x10^6cells) for 1 h at 4 degree C. The secondary antibody used was FITC goat anti-mouse IgG (H+L) at 1/200 dilution for 1 h at 4 degree C. Isotype control antibody (green line) was mouse IgG1 (10ug/1x10^6cells) used under the same conditions. Acquisition of >10,000 events was performed.)

Mouse Nestin Monoclonal Antibody | anti-NES antibody

Mouse Anti-Nestin monoclonal Antibody

Gene Names
NES; Nbla00170
Applications
ELISA, Western Blot, Immunohistochemistry, Immunofluorescence, Flow Cytometry, Functional Assay
Purity
>95%, Protein G Purified
Synonyms
Nestin; Monoclonal Antibody; Mouse Anti-Nestin monoclonal Antibody; Nbla00170; anti-NES antibody
Ordering
For Research Use Only!
Host
Mouse
Clonality
Monoclonal
Isotype
IgG1
Specificity
Specific for Human Nestin denatured and native forms
Purity/Purification
>95%, Protein G Purified
Sequence Length
1621
Applicable Applications for anti-NES antibody
ELISA (EIA), Western Blot (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FC/FACS)
Storage Buffer
Preservative: 0.03% Proclin 300
Constituents: 50% Glycerol, 0.01M PBS, PH 7.4
Conjugate
Non-conjugated
Immunogen
Recombinant nestin Protein
Santa Cruz Alternative
Potential replacement for Santa Cruz Biotechnology antibody catalog# sc-23927 / sc-71665 / sc-73489
Preparation and Storage
Shipped at 4 degree C. Upon delivery aliquot and store at -20 degree C or -80 degree C. Avoid repeated freeze.

Application Data

(Overlay histogram showing Hela cells stained with AAA18857 (red line). The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min. The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (10ug/1x10^6cells) for 1 h at 4 degree C. The secondary antibody used was FITC goat anti-mouse IgG (H+L) at 1/200 dilution for 1 h at 4 degree C. Isotype control antibody (green line) was mouse IgG1 (10ug/1x10^6cells) used under the same conditions. Acquisition of >10,000 events was performed.)

Application Data (Overlay histogram showing Hela cells stained with AAA18857 (red line). The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min. The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (10ug/1x10^6cells) for 1 h at 4 degree C. The secondary antibody used was FITC goat anti-mouse IgG (H+L) at 1/200 dilution for 1 h at 4 degree C. Isotype control antibody (green line) was mouse IgG1 (10ug/1x10^6cells) used under the same conditions. Acquisition of >10,000 events was performed.)

Application Data

(Overlay histogram showing U251 cells stained with AAA18857 (red line). The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min. The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (10ug/1x10^6cells) for 1 h at 4 degree C. The secondary antibody used was FITC goat anti-mouse IgG (H+L) at 1/200 dilution for 1 h at 4 degree C. Isotype control antibody (green line) was mouse IgG1 (10ug/1x10^6cells) used under the same conditions. Acquisition of >10,000 events was performed.)

Application Data (Overlay histogram showing U251 cells stained with AAA18857 (red line). The cells were fixed with 70% Ethylalcohol (18h) and then permeabilized with 0.3% Triton X-100 for 2 min. The cells were then incubated in 1x PBS /10% normal goat serum to block non-specific protein-protein interactions followed by the antibody (10ug/1x10^6cells) for 1 h at 4 degree C. The secondary antibody used was FITC goat anti-mouse IgG (H+L) at 1/200 dilution for 1 h at 4 degree C. Isotype control antibody (green line) was mouse IgG1 (10ug/1x10^6cells) used under the same conditions. Acquisition of >10,000 events was performed.)

IF (Immunofluorescence)

(Immunofluorescent analysis of U251 cells using AAA18857 at a dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L))

IF (Immunofluorescence) (Immunofluorescent analysis of U251 cells using AAA18857 at a dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L))

IF (Immunofluorescence)

(Immunofluorescent analysis of PC-3 cells using AAA18857 at a dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L))

IF (Immunofluorescence) (Immunofluorescent analysis of PC-3 cells using AAA18857 at a dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L))

IF (Immunofluorescence)

(Immunofluorescent analysis of Hela cells using AAA18857 at a dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L))

IF (Immunofluorescence) (Immunofluorescent analysis of Hela cells using AAA18857 at a dilution of 1:100 and Alexa Fluor 488-congugated AffiniPure Goat Anti-Mouse IgG(H+L))

IHC (Immunohistochemistry)

(Immunohistochemistry of paraffin-embedded human melanoma using AAA18857 at dilution of 1:100.)

IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human melanoma using AAA18857 at dilution of 1:100.)

IHC (Immunohistochemistry)

(Immunohistochemistry of paraffin-embedded human kidney tissue using AAA18857 at dilution of 1:100.)

IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human kidney tissue using AAA18857 at dilution of 1:100.)

IHC (Immunohistochemistry)

(Immunohistochemistry of paraffin-embedded human tonsil tissue using AAA18857 at dilution of 1:100.)

IHC (Immunohistochemistry) (Immunohistochemistry of paraffin-embedded human tonsil tissue using AAA18857 at dilution of 1:100.)

WB (Western Blot)

(Western Blot Positive WB detected in: U251 whole cell lysate, SH-Sy5y whole cell lysate All lanes: NES antibody at 3 ug/mlPredicted band size: 260 kDa Observed band size: 260 kDa )

WB (Western Blot) (Western Blot Positive WB detected in: U251 whole cell lysate, SH-Sy5y whole cell lysate All lanes: NES antibody at 3 ug/mlPredicted band size: 260 kDa Observed band size: 260 kDa )
Related Product Information for anti-NES antibody
Required for brain and eye development. Promotes the disassembly of phosphorylated vimentin intermediate filaments (IF) during mitosis and may play a role in the trafficking and distribution of IF proteins and other cellular factors to daughter cells during progenitor cell division. Required for survival, renewal and mitogen-stimulated proliferation of neural progenitor cells.

NCBI and Uniprot Product Information

NCBI GI #
NCBI GeneID
NCBI Accession #
NCBI GenBank Nucleotide #
UniProt Accession #
Molecular Weight
177,439 Da
NCBI Official Full Name
nestin
NCBI Official Synonym Full Names
nestin
NCBI Official Symbol
NES
NCBI Official Synonym Symbols
Nbla00170
NCBI Protein Information
nestin
UniProt Protein Name
Nestin
UniProt Gene Name
NES
UniProt Entry Name
NEST_HUMAN

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Product Notes

The NES nes (Catalog #AAA18857) is an Antibody produced from Mouse and is intended for research purposes only. The product is available for immediate purchase. AAA Biotech's Nestin can be used in a range of immunoassay formats including, but not limited to, ELISA (EIA), Western Blot (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (FC/FACS). Researchers should empirically determine the suitability of the NES nes for an application not listed in the data sheet. Researchers commonly develop new applications and it is an integral, important part of the investigative research process. It is sometimes possible for the material contained within the vial of "Nestin, Monoclonal Antibody" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.

Precautions

All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.

Disclaimer

Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.

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