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EVC2 antibody, C-term

Anti-EVC2 antibody, C-term used in IHC (Paraffin sections) (IHC-P). GTX89863

Cat. No. GTX89863

Host

 Goat

Clonality

 Polyclonal

Isotype

 IgG

Application

 IHC-P

Reactivity

 Human
Package
100 μg ($419)
See all EVC2 products

APPLICATION

Application Note

*Optimal dilutions/concentrations should be determined by the researcher.
Application Recommended Dilution
IHC-P 2-4μg/ml

Note :

IHC-P
Human Placenta shows strong staining of the cytotrophoblasts.
Not tested in other applications.

Positive Control

The peptide used to generate this antibody is available for purchase (GTX89863-PEP).

Product Note

This antibody is expected to recognise isoform 1 (NP_667338.3) and isoform 2 (NP_001159608.1).

PROPERTIES

Form

Liquid

Buffer

TBS, 0.5% BSA

Preservative

0.02% Sodium azide

Storage

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

Concentration

0.50 mg/ml (Please refer to the vial label for the specific concentration.)

Antigen Species

Human

Immunogen

Peptide with sequence C-LNAKKAMRALGMD, from the C Terminus of the protein sequence according to NP_667338.3; NP_001159608.1.

Purification

Purified by ammonium sulphate precipitation followed by antigen affinity chromatography

Conjugation

Unconjugated

Note

For laboratory research use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.

Purchasers shall not, and agree not to enable third parties to, analyze, copy, reverse engineer or otherwise attempt to determine the structure or sequence of the product.

TARGET

Synonyms

EvC ciliary complex subunit 2 , LBN , WAD

Cellular Localization

Cell membrane , Nucleus

Background

This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Oct 2009]

Database

Research Area

DATA IMAGES

Anti-EVC2 antibody, C-term used in IHC (Paraffin sections) (IHC-P). GTX89863

GTX89863 IHC-P Image

IHC-P analysis of human placenta using GTX89863 EVC2 antibody, C-term.
Antigen retrieval : citrate buffer pH 6
Dilution : 2μg/ml

REFERENCE

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REVIEW

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SDS
Sodium Azide.pdf
Package List Price ($)
$ 419