EML1 Antibody - BSA Free

Novus Biologicals | Catalog # NBP3-46572

Novus Biologicals
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Key Product Details

Species Reactivity

Human, Mouse, Rat

Applications

Western Blot, ELISA, Immunocytochemistry/ Immunofluorescence

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Format

BSA Free
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Product Specifications

Immunogen

echinoderm microtubule associated protein like 1. (Uniprot# O00423)

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Theoretical MW

90 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Scientific Data Images for EML1 Antibody - BSA Free

EML1 Antibody - BSA Free

Immunocytochemistry/ Immunofluorescence: EML1 Antibody - BSA Free [NBP3-46572] -

Immunocytochemistry/ Immunofluorescence: EML1 Antibody - BSA Free [NBP3-46572] - Immunofluorescent analysis of HepG2 cells, using EML1 antibody at 1:25 dilution and Rhodamine-labeled goat anti-rabbit IgG (EML1
EML1 Antibody - BSA Free

Western Blot: EML1 Antibody - BSA Free [NBP3-46572] -

Western Blot: EML1 Antibody - BSA Free [NBP3-46572] - HepG2 cells were subjected to SDS PAGE followed by western blot with (EML1 antibody) at dilution of 1:300

Applications for EML1 Antibody - BSA Free

Application
Recommended Usage

Immunocytochemistry/ Immunofluorescence

1:10-1:100

Western Blot

1:500-1:2000

Formulation, Preparation, and Storage

Purification

Immunogen affinity purified

Formulation

PBS, 50% Glycerol, pH (7.3)

Format

BSA Free

Preservative

0.02% Sodium Azide

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at -20C. Avoid freeze-thaw cycles.

Background: EML1

Human echinoderm microtubule-associated protein-like is a strong candidate for the Usher syndrome type 1A gene. Usher syndromes (USHs) are a group of genetic disorders consisting of congenital deafness, retinitis pigmentosa, and vestibular dysfunction of variable onset and severity depending on the genetic type. The disease process in USHs involves the entire brain and is not limited to the posterior fossa or auditory and visual systems. The USHs are catagorized as type I (USH1A, USH1B, USH1C, USH1D, USH1E and USH1F), type II (USH2A and USH2B) and type III (USH3). The type I is the most severe form. Gene loci responsible for these three types are all mapped. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]

Alternate Names

echinoderm microtubule associated protein like 1, ELP79, EMAP1, EMAP-1, EMAPechinoderm microtubule-associated protein-like 1, EMAPL1, EMAPLhuEMAP-1, FLJ45033, HuEMAP, HuEMAP-1

Gene Symbol

EML1

Additional EML1 Products

Product Documents for EML1 Antibody - BSA Free

Certificate of Analysis

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Product Specific Notices for EML1 Antibody - BSA Free

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Protocols

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