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Creative Biolabs

NeuroMab™ Anti-SEZ6 Antibody(NRP-0422-P509)

[CAT#: NRP-0422-P509] Review(5) Q&As(3)

A functional antibody raised against Human, Mouse, Rat SEZ6.

Host Species:
Mouse
Species Reactivity:
Human; Mouse; Rat
Applications:
FC; IHC; In Vitro; In Vivo

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Product Overview

Description

The antibody specifically binds to a human SEZ6 protein, use for the treatment, diagnosis or prophylaxis of neoplastic disorders.

Immunogen

ECD portion of the human EZ6

Species Reactivity

Human; Mouse; Rat

Clonality

Monoclonal

Host Species

Mouse

Applications

FC; IHC; In Vitro; In Vivo

Relevant Diseases

Epilepsy
Product Properties

Formulation

PBS only

Preservatives

BSA Free

Concentration

1mg/mL

Purification

Purified recombinant IgG prepared by affinity chromatography on Protein A from a mammalian cell line

Purity

>95% by SDS PAGE or HPLC

Endotoxin Level

Regular Endotoxin < 5 EU/mg
Low Endotoxin < 1 EU/mg

Shipping

Gel Packs

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze-thaw cycles.

Research Use Only

For research use only
Target

Target

SEZ6

Official Name

SEZ6

Full Name

Seizure Related 6 Homolog

Alternative Names

Seizure Related 6 Homolog; Seizure Related 6 Homolog (Mouse); Seizure Protein 6 Homolog; HSEZ-6; BSRPC; SEZ-6;

Gene ID

20370(Mouse); 192247(Rat)

Uniprot ID

Q7TSK2(Mouse)
Product Pictures
FCM

Figure 1 shows the detection of SEZ6 protein expression in NTX tumor cells by flow cytometry using various anti-SEZ6 antibodies.

Axis corresponds to concentration of 3E antibody (Fab) and Y axis corresponds to NGF binding (percentage of maximal UR). Increasing concentrations of Fab E3 blocked the interaction of NGF with p75 and trkA, as indicated by a decrease in signal (measured in UR). When the concentration of E3 antibody (Fab) was equal to that of NGF, no NGF binding was observed (indicated by zero signal).

FuncS

Figure 2 shows the results of an in vitro disruption assay using anti-SEZ6 ADCs in HEK293 cells overexpressing SEZ6.

Axis corresponds to concentration of 3E antibody (Fab) and Y axis corresponds to NGF binding (percentage of maximal UR). Increasing concentrations of Fab E3 blocked the interaction of NGF with p75 and trkA, as indicated by a decrease in signal (measured in UR). When the concentration of E3 antibody (Fab) was equal to that of NGF, no NGF binding was observed (indicated by zero signal).

FuncS

Figure 3 shows the effect of anti-SEZ6 ADCs on the growth of SCLC (LU86) and LCNEC (Lu50) tumors in vivo.

Axis corresponds to concentration of 3E antibody (Fab) and Y axis corresponds to NGF binding (percentage of maximal UR). Increasing concentrations of Fab E3 blocked the interaction of NGF with p75 and trkA, as indicated by a decrease in signal (measured in UR). When the concentration of E3 antibody (Fab) was equal to that of NGF, no NGF binding was observed (indicated by zero signal).

FuncS

Figure 4 shows the ability of conjugated humanized anti-SEZ6 antibodies to delay the growth of four SCLC tumors (LU80, LU64, LU111 and LU117) in vivo and achieve durable remission in immunosuppressed mice.

Axis corresponds to concentration of 3E antibody (Fab) and Y axis corresponds to NGF binding (percentage of maximal UR). Increasing concentrations of Fab E3 blocked the interaction of NGF with p75 and trkA, as indicated by a decrease in signal (measured in UR). When the concentration of E3 antibody (Fab) was equal to that of NGF, no NGF binding was observed (indicated by zero signal).

FuncS

Figure 5 shows the ability of conjugated humanized anti-SEZ6 antibodies to delay the growth of four SCLC tumors (LU80, LU64, LU111 and LU117) in vivo and achieve durable remission in immunosuppressed mice.

Axis corresponds to concentration of 3E antibody (Fab) and Y axis corresponds to NGF binding (percentage of maximal UR). Increasing concentrations of Fab E3 blocked the interaction of NGF with p75 and trkA, as indicated by a decrease in signal (measured in UR). When the concentration of E3 antibody (Fab) was equal to that of NGF, no NGF binding was observed (indicated by zero signal).

Publications

Publications (0)

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Customer Reviews and Q&As
Customer Reviews Average Customer Ratings Overall
5.0
user
Excellent
A fantastic addition to our lab
We've used it extensively in our flow cytometry experiments and found it to be highly specific with minimal background noise. The results have significantly improved the quality of our research on neural pathways.
user
Excellent
Highly recommend it to other researchers
The antibody binds specifically to SEZ6, and we observed robust and reproducible staining. The product has contributed to our understanding of SEZ6's role in neurodevelopment, and we plan to continue using it in future studies.
user
Excellent
The antibody provided clear and distinct staining of SEZ6 in brain tissue samples
Its high specificity and low background have made our imaging results very reliable. We are extremely satisfied with the performance of this antibody.
user
Excellent
We are very pleased with the results
The antibody showed excellent specificity and sensitivity in our mouse models. It has allowed us to visualize SEZ6 expression in a way that was not possible with other antibodies.
user
Excellent
High accuracy
We've used it for both in vitro and in vivo experiments and found it to be highly specific and reliable. The antibody provided consistent and clear results, which has been crucial for our research on neural cell markers.
Q&As
How can I be sure that the antibody will work in my specific experimental conditions?
We provide detailed product datasheets, including recommended protocols and validation data, to help ensure successful use of the antibody in various experimental conditions. Additionally, our technical support team is available to provide guidance on protocol optimization and troubleshooting. If the antibody does not perform as expected, we offer a satisfaction guarantee and will work with you to resolve any issues.
What type of secondary antibody should I use with this antibody?
The choice of secondary antibody depends on the host species of the primary antibody and the detection method you plan to use. The antibody is a mouse monoclonal antibody, so an anti-mouse IgG secondary antibody conjugated to a suitable enzyme (e.g., HRP) or fluorophore (e.g., Alexa Fluor) is recommended. Ensure the secondary antibody is compatible with your detection system.
How can I determine the optimal antibody concentration for my experiments?
To determine the optimal concentration for your specific experiments, we recommend performing a titration experiment. Start with the suggested dilution range provided in the datasheet and test a series of dilutions to find the concentration that provides the best signal-to-noise ratio. This ensures the antibody performs optimally in your experimental conditions.
For Research Use Only. Not For Clinical Use.
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