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PEA-15 Antibodies

We offer PEA-15 Antibodies for use in common research applications: ELISA, Immunocytochemistry/Immunofluorescence, Immunohistochemistry, Immunohistochemistry-Paraffin, Western Blot. Each PEA-15 Antibody is fully covered by our Guarantee+, to give you complete peace of mind and the support when you need it. Our PEA-15 Antibodies can be used in a variety of model species: Human, Mouse, Rat. Use the list below to choose the PEA-15 Antibody which is most appropriate for your research; you can click on each one to view full technical details, images, references, reviews and related products. Choose from our PEA-15 polyclonal antibodies.

Alternate Names for PEA-15 Antibodies

anti-PEA-15 antibody, anti-PEA15 antibody, anti-HMAT115kD antibody, anti-PED15 kDa phosphoprotein enriched in astrocytes antibody, anti-phosphoprotein enriched in astrocytes 15 antibody, anti-Phosphoprotein enriched in diabetes antibody

9 Results for "pea-15" in Primary Antibodies

AF5588

PEA-15 Antibody

(1 Publication)

100 μg

AF5588

Western blot shows lysates of A172 human glioblastoma cell line and human cortex tissue. PVDF membrane was probed with 1 µg/mL of Sheep Anti-Human/Mouse PEA-15 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5588) followed by HRP-conjugated Anti-Sheep IgG Secondary Antibody (Catalog # HAF016). A specific band was detected for PEA-15 at approximately 15 kDa (as indicated). This experiment was conducted under reducing conditions and using Immunoblot Buffer Group 8.

PEA-15 was detected in immersion fixed paraffin-embedded sections of human brain (cortex) using Sheep Anti-Human/Mouse PEA-15 Antigen Affinity-purified Polyclonal Antibody (Catalog # AF5588) at 1 µg/mL overnight at 4 °C. Tissue was stained using the Anti-Sheep HRP-DAB Cell & Tissue Staining Kit (brown; Catalog # CTS019) and counterstained with hematoxylin (blue). Specific staining was localized to neurons. View our protocol for Chromogenic IHC Staining of Paraffin-embedded Tissue Sections.

PED is inversely correlated to HNF4 alpha expression. (a) SNU-449 cells were co-transfected with 100 ng of pPED477 PED promoter-luciferase or pGL3 basic construct and treated with siRNA against HNF4 alpha or siRNA control. Luciferase activity was normalized for Renilla activity and is presented as mean±S.D. A representative experiment in triplicate is shown. (b,c) PED expression levels in HCC samples (b; n=59) or corresponding non-tumoral liver tissue (c, n=59) were correlated with HNF4 alpha expression. Correlation was calculated by Spearman test. Data are reported as probe intensity of an mRNA transcriptome array. (d) Western blot analysis for HNF4 alpha and PED in two HCC patient tumor samples and their corresponding non-tumoral (NT) tissues. Calnexin was used as loading control. Arrow: canonical full length HNF4 alpha (52 kDa); other bands are isoforms or truncated forms of the protein. (e,f) HuH-7 and PLC/PRF/5 cell lines were transfected with siRNA against HNF4 alpha (siHNF4 alpha ) or siRNA control. After 72 h the protein expression of HNF4 alpha and PED was measured by western blot (e) and beta -actin served as control. mRNA expression was measured by qPCR (f) using RNA 18 S as internal control at 48 h for HuH-7 and 72 h for PLC/PRF/5. Data are reported as mean±S.D. of two independent experiments performed in triplicate. (g) SNU-449 cells were transfected with siRNA against HNF4 alpha or siRNA against PED alone or in combination, or siRNA control, as indicated. Migration was assessed by CIM plate with xCELLigence apparatus after 12 h and 24 h. Data are reported as mean±S.D. of two independent experiments performed in triplicate. (h) Western blot analysis of pERKThr202/Tyr204 and ERK in SNU-449, Hep3B and HuH-7 cell lines transfected with PED-MYC. beta -Actin was used as loading control. (i) pERKThr202/Tyr204 expression in two HCC patients and their non-tumoral counterpart. Calnexin was used as loading control. *P<0.05, **P<0.01, ****P<0.0001 Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/cddis2017512), licensed under a CC-BY license. Not internally tested by R&D Systems.

PED confers resistance to sorafenib therapy. (a) HuH-7 and SNU-449 cells were transfected with siRNA against PED or siRNA control. Afterwards, HuH-7 and SNU-449 cells were treated with 10 μM and 20 μm respectively of sorafenib or left untreated. Cell growth was evaluated by using the xCELLigence instrument at the indicated time. Data are reported as mean±S.D. of two independent experiments performed in triplicate. (b) HuH-7 and Hep3B cells were transfected with PED-MYC vector for 24 h and then seeded in a 96-well plate. 10 μm of sorafenib was added and 24 h or 48 h later, cell viability was measured by a MTT assay. Data are reported as mean±S.D. of two independent experiments perfomed in triplicate. (c) HuH-7 cells were transfected with PED-MYC or empty vector (Ctrl) and siRNA against PED or siRNA control (Ctrl), as indicated. After 24 h, cells were treated with 10 μM or 7 μM sorafenib, respectively, for 48 h and caspase-3 activation was measured by western blot. (d) HuH-7 cells were transfected with siRNA against PED or control siRNA. Afterwards, cells were treated with 10 μM sorafenib and 48 h later caspase-3/7 assay activation was measured. Data are reported as mean±SD of one experiment performed in triplicate. *P<0.1, **P<0.01, ***P<0.001, ****P<0.0001 Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/cddis2017512), licensed under a CC-BY license. Not internally tested by R&D Systems.

PED is inversely correlated to HNF4 alpha expression. (a) SNU-449 cells were co-transfected with 100 ng of pPED477 PED promoter-luciferase or pGL3 basic construct and treated with siRNA against HNF4 alpha or siRNA control. Luciferase activity was normalized for Renilla activity and is presented as mean±S.D. A representative experiment in triplicate is shown. (b,c) PED expression levels in HCC samples (b; n=59) or corresponding non-tumoral liver tissue (c, n=59) were correlated with HNF4 alpha expression. Correlation was calculated by Spearman test. Data are reported as probe intensity of an mRNA transcriptome array. (d) Western blot analysis for HNF4 alpha and PED in two HCC patient tumor samples and their corresponding non-tumoral (NT) tissues. Calnexin was used as loading control. Arrow: canonical full length HNF4 alpha (52 kDa); other bands are isoforms or truncated forms of the protein. (e,f) HuH-7 and PLC/PRF/5 cell lines were transfected with siRNA against HNF4 alpha (siHNF4 alpha ) or siRNA control. After 72 h the protein expression of HNF4 alpha and PED was measured by western blot (e) and beta -actin served as control. mRNA expression was measured by qPCR (f) using RNA 18 S as internal control at 48 h for HuH-7 and 72 h for PLC/PRF/5. Data are reported as mean±S.D. of two independent experiments performed in triplicate. (g) SNU-449 cells were transfected with siRNA against HNF4 alpha or siRNA against PED alone or in combination, or siRNA control, as indicated. Migration was assessed by CIM plate with xCELLigence apparatus after 12 h and 24 h. Data are reported as mean±S.D. of two independent experiments performed in triplicate. (h) Western blot analysis of pERKThr202/Tyr204 and ERK in SNU-449, Hep3B and HuH-7 cell lines transfected with PED-MYC. beta -Actin was used as loading control. (i) pERKThr202/Tyr204 expression in two HCC patients and their non-tumoral counterpart. Calnexin was used as loading control. *P<0.05, **P<0.01, ****P<0.0001 Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/cddis2017512), licensed under a CC-BY license. Not internally tested by R&D Systems.

PED is inversely correlated to HNF4 alpha expression. (a) SNU-449 cells were co-transfected with 100 ng of pPED477 PED promoter-luciferase or pGL3 basic construct and treated with siRNA against HNF4 alpha or siRNA control. Luciferase activity was normalized for Renilla activity and is presented as mean±S.D. A representative experiment in triplicate is shown. (b,c) PED expression levels in HCC samples (b; n=59) or corresponding non-tumoral liver tissue (c, n=59) were correlated with HNF4 alpha expression. Correlation was calculated by Spearman test. Data are reported as probe intensity of an mRNA transcriptome array. (d) Western blot analysis for HNF4 alpha and PED in two HCC patient tumor samples and their corresponding non-tumoral (NT) tissues. Calnexin was used as loading control. Arrow: canonical full length HNF4 alpha (52 kDa); other bands are isoforms or truncated forms of the protein. (e,f) HuH-7 and PLC/PRF/5 cell lines were transfected with siRNA against HNF4 alpha (siHNF4 alpha ) or siRNA control. After 72 h the protein expression of HNF4 alpha and PED was measured by western blot (e) and beta -actin served as control. mRNA expression was measured by qPCR (f) using RNA 18 S as internal control at 48 h for HuH-7 and 72 h for PLC/PRF/5. Data are reported as mean±S.D. of two independent experiments performed in triplicate. (g) SNU-449 cells were transfected with siRNA against HNF4 alpha or siRNA against PED alone or in combination, or siRNA control, as indicated. Migration was assessed by CIM plate with xCELLigence apparatus after 12 h and 24 h. Data are reported as mean±S.D. of two independent experiments performed in triplicate. (h) Western blot analysis of pERKThr202/Tyr204 and ERK in SNU-449, Hep3B and HuH-7 cell lines transfected with PED-MYC. beta -Actin was used as loading control. (i) pERKThr202/Tyr204 expression in two HCC patients and their non-tumoral counterpart. Calnexin was used as loading control. *P<0.05, **P<0.01, ****P<0.0001 Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/cddis2017512), licensed under a CC-BY license. Not internally tested by R&D Systems.

PED is overexpressed in HCC samples. (a) PED expression levels in HCC samples and their matched non-tumoral (NT) counterpart measured by an mRNA gene expression microarray. Data are reported as probe intensity. (b) PED mRNA was measured by qRT-PCR in a separate cohort of 14 HCC patients and compared with the 10 available non-tumoral counterpart. 18 S was used as internal control and 2− delta delta Ct formula was applied to determine relative expression levels. Statistical analysis (a,b) with paired Student t-test. (c) Representative immunohistochemical staining from an HCC tumor (left) with positive (3+) PED staining and non-tumoral liver tissue (NT) showing negative PED staining (right). Scale bar=20 μm. (d) Percentage and h-score (staining intensity × percentage of positive tumor cells) of PED positivity in HCC samples and non-tumoral (NT) liver tissues by immunohistochemistry. (e) Western blot analysis of total PED and phosphorylated PED (PED S116 and PED S104) in two HCC patient samples and their corresponding NT control tissues. Calnexin was used as internal control. *P<0.05, ***P<0.001 Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/cddis2017512), licensed under a CC-BY license. Not internally tested by R&D Systems.

PED modulates cell migration. (a) Western blot analysis of PED protein expression in 10 different HCC cell lines. beta -Actin was used as loading control. (b) HuH-7 and SNU-449 cells were transfected with PED-MYC or an empty control vector as wells as with siRNA against PED (siRNA PED) or control siRNA. Cell growth properties were evaluated by using xCELLigence instrument at the time indicated. Data are reported as mean±S.D. of two independent experiments performed at least in triplicate. Difference was evaluated between PED overexpressing (PED-MYC), PED silenced (siRNA PED), empty vector transfected and a siRNA control transfected cells (two-way ANOVA test). (c) HLE, SNU-449 and HuH-7 cell lines were transfected with a vector overexpressing PED (PED-MYC) or empty control vector, siRNA against PED (siRNA PED) or siRNA control. Migration was assessed using a transwell assay after 24 h. One representative image of crystal violet stained cells at 100 × is shown above and quantification by colorimetry below. ***P<0.001, ****P<0.0001 Image collected and cropped by CiteAb from the following publication (//www.nature.com/articles/cddis2017512), licensed under a CC-BY license. Not internally tested by R&D Systems.

Reactivity:

Hu, Mu

Species Glossary

Reactivity: Hu, Mu

Applications:

,

Applications: ,

Host:

Sheep Polyclonal

Host: Sheep Polyclonal

Sizes:

Sample Size Available

Sizes: Sample Size Available

Conjugate:

Unconjugated

Available Formulations

Formulation	Catalog #	Availability	Price
Carrier Free	AF5588-SP

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NBP3-05544

PEA-15 Antibody (4D2)

100 ul

NBP3-05544

Immunocytochemistry/Immunofluorescence: PEA-15 Antibody [NBP3-05544] - Western blot analysis of different tissue lysates using PEA-15 Antibody at a dilution of 1:1,000 in green: [1] protein standard (red), [2] rat whole brain, [3] rat cerebellum, [4] mouse whole brain, [5] cow cortex and [6] cow cerebellum. The single strong band at about 15kDa corresponds to the PEA-15 protein.

Immunocytochemistry/Immunofluorescence: PEA-15 Antibody [NBP3-05544] - Immunofluorescent analysis of rat brain section stained with PEA-15 Antibody at a dilution of 1:1,000 in red, and costained with rabbit pAb to GFAP at a dilution of 1:5,000 in green. The blue is Hoechst staining of nuclear DNA. Following transcardial perfusion of rat with 4% paraformaldehyde, brain was post fixed for 24 hours, cut to 45uM, and free-floating sections were stained with above antibodies. The PEA-15 antibody labels the cytoplasm of certain cells which are not labelled by the astrocyte specific GFAP antibody

Reactivity:

Hu, Mu, Rt, Bv

Species Glossary

Reactivity: Hu, Mu, Rt, Bv

Applications:

, ,

Applications: , ,

Host:

Mouse Monoclonal

Host: Mouse Monoclonal

Sizes:

Sample Size Available

Sizes: Sample Size Available

Conjugate:

Unconjugated

Available Conjugates:

Conjugate	Catalog #	Availability	Size	Price
Alexa Fluor 350	NBP3-05544AF350
Alexa Fluor 405	NBP3-05544AF405
Alexa Fluor 488	NBP3-05544AF488
Alexa Fluor 532	NBP3-05544AF532
Alexa Fluor 594	NBP3-05544AF594
Alexa Fluor 647	NBP3-05544AF647
Alexa Fluor 700	NBP3-05544AF700
Alexa Fluor 750	NBP3-05544AF750
Allophycocyanin	NBP3-05544APC
Biotin	NBP3-05544B
CoraFluor 1	NBP3-05544CL1
DyLight 350	NBP3-05544UV
DyLight 405	NBP3-05544V
DyLight 488	NBP3-05544G
DyLight 550	NBP3-05544R
DyLight 594	NBP3-05544DL594
DyLight 650	NBP3-05544C
DyLight 680	NBP3-05544FR
DyLight 755	NBP3-05544IR
FITC	NBP3-05544F
HRP	NBP3-05544H
Janelia Fluor 525	NBP3-05544JF525
Janelia Fluor 549	NBP3-05544JF549
Janelia Fluor 646	NBP3-05544JF646
Janelia Fluor 669	NBP3-05544JF669
PE	NBP3-05544PE
PerCP	NBP3-05544PCP
mFluor Violet 450 SE	NBP3-05544MFV450
mFluor Violet 500 SE	NBP3-05544MFV500
mFluor Violet 610 SE	NBP3-05544MFV610

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NBP3-05543

PEA-15 Antibody (4D117)

100 ul

NBP3-05543

Western Blot: PEA-15 Antibody [NBP3-05543] - Western blot analysis of different tissue lysates using PEA-15 Antibody at a dilution of 1:1,000 in green: [1] protein standard (red), [2] rat whole brain, [3] rat cerebellum, [4] mouse whole brain, [5] cow cortex and [6] cow cerebellum. The strong band at about 15kDa corresponds to the PEA-15 protein.

Immunocytochemistry/Immunofluorescence: PEA-15 Antibody [NBP3-05543] - Immunofluorescent analysis of rat brain section stained with PEA-15 Antibody at a dilution of 1:1,000 in red, and costained with chicken pAb to MAP2 at a dilution of 1:5,000 in green. The blue is Hoechst staining of nuclear DNA. Following transcardial perfusion of rat with 4% paraformaldehyde, brain was post fixed for 24 hours, cut to 45uM, and free-floating sections were stained with above antibodies. The PEA-15 antibody labels the cytoplasm of certain presumably neuronal cells which are not labelled by the astrocyte specific GFAP antibody.

Reactivity:

Hu, Mu, Rt, Bv

Species Glossary

Reactivity: Hu, Mu, Rt, Bv

Applications:

,

Applications: ,

Host:

Mouse Monoclonal

Host: Mouse Monoclonal

Sizes:

Sample Size Available

Sizes: Sample Size Available

Conjugate:

Unconjugated

Available Conjugates:

Conjugate	Catalog #	Availability	Size	Price
Alexa Fluor 350	NBP3-05543AF350
Alexa Fluor 405	NBP3-05543AF405
Alexa Fluor 488	NBP3-05543AF488
Alexa Fluor 532	NBP3-05543AF532
Alexa Fluor 594	NBP3-05543AF594
Alexa Fluor 647	NBP3-05543AF647
Alexa Fluor 700	NBP3-05543AF700
Alexa Fluor 750	NBP3-05543AF750
Allophycocyanin	NBP3-05543APC
Biotin	NBP3-05543B
CoraFluor 1	NBP3-05543CL1
DyLight 350	NBP3-05543UV
DyLight 405	NBP3-05543V
DyLight 488	NBP3-05543G
DyLight 550	NBP3-05543R
DyLight 594	NBP3-05543DL594
DyLight 650	NBP3-05543C
DyLight 680	NBP3-05543FR
DyLight 755	NBP3-05543IR
FITC	NBP3-05543F
HRP	NBP3-05543H
Janelia Fluor 525	NBP3-05543JF525
Janelia Fluor 549	NBP3-05543JF549
Janelia Fluor 646	NBP3-05543JF646
Janelia Fluor 669	NBP3-05543JF669
PE	NBP3-05543PE
PerCP	NBP3-05543PCP
mFluor Violet 450 SE	NBP3-05543MFV450
mFluor Violet 500 SE	NBP3-05543MFV500
mFluor Violet 610 SE	NBP3-05543MFV610

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NBP2-88031

PEA-15 Antibody

100 ul

NBP2-88031

Western Blot: PEA-15 Antibody [NBP2-88031] - WB Suggested Anti-PEA15 Antibody Titration: 0.2-1 ug/ml. ELISA Titer: 1:1562500. Positive Control: Human brain

Immunohistochemistry-Paraffin: PEA-15 Antibody [NBP2-88031] - Rabbit Anti-PEA15 Antibody. Formalin Fixed Paraffin Embedded Tissue: Human heart Tissue. Observed Staining: Cytoplasmic. Primary Antibody Concentration: 1:100.

Western Blot: PEA-15 Antibody [NBP2-88031] - WB Suggested Anti-PEA15 Antibody. Positive Control: Lane 1: 20ug EGFP-transfected MCF7 lysate Lane 2: 20ug EGFP-PEA15 transfected MCF7 lysate. Primary Antibody Dilution : 1:1000. Secondary Antibody : Goat anti-rabbit-HRP. Secondry Antibody Dilution : 1:50

Reactivity:

Hu

Species Glossary

Reactivity: Hu

Applications:

,

Applications: ,

Host:

Rabbit Polyclonal

Host: Rabbit Polyclonal

Conjugate:

Unconjugated

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NBP2-62670

PEA-15 Antibody

100 ul

NBP2-62670

Immunohistochemistry-Paraffin: PEA-15 Antibody [NBP2-62670] - Staining of human cerebral cortex shows high expression.

<b>Orthogonal Strategies Validation. </b>Immunohistochemistry-Paraffin: PEA-15 Antibody [NBP2-62670] - Analysis in human cerebral cortex and colon tissues using Anti-PEA15 antibody. Corresponding PEA15 RNA-seq data are presented for the same tissues.

Immunohistochemistry-Paraffin: PEA-15 Antibody [NBP2-62670] - Staining of human colon shows low expression as expected.

Reactivity:

Hu

Species Glossary

Reactivity: Hu

Applications:

Applications:

Host:

Rabbit Polyclonal

Host: Rabbit Polyclonal

Sizes:

Sample Size Available

Sizes: Sample Size Available

Conjugate:

Unconjugated

Validated by:

Validated by:

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NBP2-93741

PEA-15 Antibody - BSA Free

0.1 ml

NBP2-93741

Western Blot: PEA-15 Antibody [NBP2-93741] - Analysis of extracts of various cell lines, using PEA-15 at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit . Exposure time: 90s.

Reactivity:

Hu, Mu

Species Glossary

Reactivity: Hu, Mu

Applications:

Applications:

Host:

Rabbit Polyclonal

Host: Rabbit Polyclonal

Sizes:

Sample Size Available

Sizes: Sample Size Available

Conjugate:

Unconjugated

Available Formulations

Formulation	Catalog #	Availability	Price
BSA Free	NBP2-93741-0.02ml

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NBP1-81732

PEA-15 Antibody

0.1 ml

NBP1-81732

Immunocytochemistry/Immunofluorescence: PEA-15 Antibody [NBP1-81732] - Staining of human cell line U-2 OS shows localization to nucleus & cytosol. Antibody staining is shown in green.

Reactivity:

Hu, Mu, Rt

Species Glossary

Reactivity: Hu, Mu, Rt

Applications:

Applications:

Host:

Rabbit Polyclonal

Host: Rabbit Polyclonal

Sizes:

Sample Size Available

Sizes: Sample Size Available

Conjugate:

Unconjugated

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NBP3-05544JF669

PEA-15 Antibody (4D2) [Janelia Fluor® 669]

0.1 ml

Reactivity:

Hu, Mu, Rt, Bv

Species Glossary

Reactivity: Hu, Mu, Rt, Bv

Applications:

, ,

Applications: , ,

Host:

Mouse Monoclonal

Host: Mouse Monoclonal

Conjugate:

Janelia Fluor 669

Available Conjugates:

Conjugate	Catalog #	Availability	Size	Price
Alexa Fluor 350	NBP3-05544AF350
Alexa Fluor 405	NBP3-05544AF405
Alexa Fluor 488	NBP3-05544AF488
Alexa Fluor 532	NBP3-05544AF532
Alexa Fluor 594	NBP3-05544AF594
Alexa Fluor 647	NBP3-05544AF647
Alexa Fluor 700	NBP3-05544AF700
Alexa Fluor 750	NBP3-05544AF750
Allophycocyanin	NBP3-05544APC
Biotin	NBP3-05544B
CoraFluor 1	NBP3-05544CL1
DyLight 350	NBP3-05544UV
DyLight 405	NBP3-05544V
DyLight 488	NBP3-05544G
DyLight 550	NBP3-05544R
DyLight 594	NBP3-05544DL594
DyLight 650	NBP3-05544C
DyLight 680	NBP3-05544FR
DyLight 755	NBP3-05544IR
FITC	NBP3-05544F
HRP	NBP3-05544H
Janelia Fluor 525	NBP3-05544JF525
Janelia Fluor 549	NBP3-05544JF549
Janelia Fluor 585	NBP3-05544JF585
Janelia Fluor 635	NBP3-05544JF635
Janelia Fluor 646	NBP3-05544JF646
PE	NBP3-05544PE
PerCP	NBP3-05544PCP
mFluor Violet 450 SE	NBP3-05544MFV450
mFluor Violet 500 SE	NBP3-05544MFV500
mFluor Violet 610 SE	NBP3-05544MFV610

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NBP3-05543JF669

PEA-15 Antibody (4D117) [Janelia Fluor® 669]

0.1 ml

Reactivity:

Hu, Mu, Rt, Bv

Species Glossary

Reactivity: Hu, Mu, Rt, Bv

Applications:

,

Applications: ,

Host:

Mouse Monoclonal

Host: Mouse Monoclonal

Conjugate:

Janelia Fluor 669

Available Conjugates:

Conjugate	Catalog #	Availability	Size	Price
Alexa Fluor 350	NBP3-05543AF350
Alexa Fluor 405	NBP3-05543AF405
Alexa Fluor 488	NBP3-05543AF488
Alexa Fluor 532	NBP3-05543AF532
Alexa Fluor 594	NBP3-05543AF594
Alexa Fluor 647	NBP3-05543AF647
Alexa Fluor 700	NBP3-05543AF700
Alexa Fluor 750	NBP3-05543AF750
Allophycocyanin	NBP3-05543APC
Biotin	NBP3-05543B
CoraFluor 1	NBP3-05543CL1
DyLight 350	NBP3-05543UV
DyLight 405	NBP3-05543V
DyLight 488	NBP3-05543G
DyLight 550	NBP3-05543R
DyLight 594	NBP3-05543DL594
DyLight 650	NBP3-05543C
DyLight 680	NBP3-05543FR
DyLight 755	NBP3-05543IR
FITC	NBP3-05543F
HRP	NBP3-05543H
Janelia Fluor 525	NBP3-05543JF525
Janelia Fluor 549	NBP3-05543JF549
Janelia Fluor 585	NBP3-05543JF585
Janelia Fluor 635	NBP3-05543JF635
Janelia Fluor 646	NBP3-05543JF646
PE	NBP3-05543PE
PerCP	NBP3-05543PCP
mFluor Violet 450 SE	NBP3-05543MFV450
mFluor Violet 500 SE	NBP3-05543MFV500
mFluor Violet 610 SE	NBP3-05543MFV610

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