Soluble Calcium Activated Nucleotidase 1 (CANT1) Antibody

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195€ (20 µl)

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935106861
info@markelab.com
name
Soluble Calcium Activated Nucleotidase 1 (CANT1) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx004847
tested applications
ELISA, WB

Description

CANT1 Antibody is a Rabbit Polyclonal antibody against CANT1. This protein encoded by this gene belongs to the apyrase family. It functions as a calcium-dependent nucleotidase with a preference for UDP. Mutations in this gene are associated with Desbuquois dysplasia with hand anomalies. Alternatively spliced transcript variants have been noted for this gene.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Target: Soluble Calcium Activated Nucleotidase 1 (CANT1)
Immunogen: Recombinant protein corresponding to CANT1. The exact sequence is proprietary.
Host
Rabbit
Reactivity
Human
Assay Type
Concentration: > 0.2 mg/ml
Recommended Dilution
ELISA: 1 µg/ml, WB: 1/500 - 1/1000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Observed MW
Calculated MW: 45 kDa  Observed MW: 45 kDa
Purification
Purified by affinity chromatography.
Size 1
20 µl
Size 2
100 µl
Size 3
2 × 100 µl
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS, pH 7.3, containing 0.05% Proclin-300, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
Q8WVQ1
Gene ID
124583
NCBI Accession
NP_620148.1
Background
Antibody anti-CANT1
Status
RUO
Note
THIS PRODUCT IS FOR RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC, THERAPEUTIC OR COSMETIC PROCEDURES. NOT FOR HUMAN OR ANIMAL CONSUMPTION.

Descripción

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CANT1 Antibody is a Rabbit Polyclonal antibody against CANT1. This protein encoded by this gene belongs to the apyrase family. It functions as a calcium-dependent nucleotidase with a preference for UDP. Mutations in this gene are associated with Desbuquois dysplasia with hand anomalies. Alternatively spliced transcript variants have been noted for this gene.

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