FKTN polyclonal (Center), anti-human
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In stock
SKU
AC-AP12786c
Catalog Number: AC-AP12786c
Size: 80 µl, 400 µl
Isotype: Rabbit IgG
Clone Name: RB31283
Applications: WB, IHC-P
Datasheet
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Size: 80 µl, 400 µl
Isotype: Rabbit IgG
Clone Name: RB31283
Applications: WB, IHC-P
Datasheet
Request Information
Background:
The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.
Other Names:
Fukutin, 2---, Fukuyama-type congenital muscular dystrophy protein, FKTN, FCMD
Target/Specificity:
This FKTN antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 177-206 amino acids from the Central region of human FKTN.
Antigen Region:
177-206
Antigen Type: Synthetic Peptide
Gene Name: FKTN (HGNC:3622)
Gene ID: 2218
Primary Accession: O75072
NCBI Accession: NP_001073270.1;NP_001185892.1;NP_006722.2
Other Accession: Q60HG0; NP_001073270.1; NP_006722.2
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
The protein encoded by this gene is a putative transmembrane protein that is localized to the cis-Golgi compartment, where it may be involved in the glycosylation of alpha-dystroglycan in skeletal muscle. The encoded protein is thought to be a glycosyltransferase and could play a role in brain development. Defects in this gene are a cause of Fukuyama-type congenital muscular dystrophy (FCMD), Walker-Warburg syndrome (WWS), limb-girdle muscular dystrophy type 2M (LGMD2M), and dilated cardiomyopathy type 1X (CMD1X). Alternatively spliced transcript variants have been found for this gene.
Other Names:
Fukutin, 2---, Fukuyama-type congenital muscular dystrophy protein, FKTN, FCMD
Target/Specificity:
This FKTN antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 177-206 amino acids from the Central region of human FKTN.
Antigen Region:
177-206
Antigen Type: Synthetic Peptide
Gene Name: FKTN (HGNC:3622)
Gene ID: 2218
Primary Accession: O75072
NCBI Accession: NP_001073270.1;NP_001185892.1;NP_006722.2
Other Accession: Q60HG0; NP_001073270.1; NP_006722.2
Format: Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
| Is Featured? | No |
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