NK2 Homeobox 5 (NKX2-5) Antibody

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312€ (60 µl)

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935106861
info@markelab.com
name
NK2 Homeobox 5 (NKX2-5) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx004321
tested applications
WB

Description

NKX2-5 Antibody is a Rabbit Polyclonal antibody against NKX2-5. This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
NK2 Homeobox 5 (NKX2-5)
Host
Rabbit
Reactivity
Human, Mouse, Rat
Recommended Dilution
WB: 1/500 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
60 µl
Size 2
120 µl
Size 3
200 µl
Form
Liquid
Tested Applications
WB
Buffer
PBS, pH 7.3, containing 0.02% sodium azide, 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
P52952
Gene ID
1482
NCBI Accession
NP_004378.1
Background
Antibody anti-NKX2-5
Status
RUO
Note
Concentration: 1 mg/ml - 

Descripción

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NK2 Homeobox 5 (NKX2-5) Antibody

NKX2-5 Antibody is a Rabbit Polyclonal antibody against NKX2-5. This gene encodes a homeobox-containing transcription factor. This transcription factor functions in heart formation and development. Mutations in this gene cause atrial septal defect with atrioventricular conduction defect, and also tetralogy of Fallot, which are both heart malformation diseases. Mutations in this gene can also cause congenital hypothyroidism non-goitrous type 5, a non-autoimmune condition. Alternative splicing results in multiple transcript variants.

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