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Cytokeratin 13 (ABT-CK13) mouse mAb (Ready to Use)

-YM6163R

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Catalog: YM6163R
Size
Price
Status
Qty.
10mL
$240.00
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6mL
$180.00
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3mL
$120.00
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Main Information
Target

Cytokeratin 13

Host Species

Mouse

Reactivity

Human,

Applications

IHC

Conjugate/Modification


Unmodified

Detailed Information
Recommended Dilution Ratio
Ready to use for IHC
Formulation
The prediluted ready-to-use antibody is diluted in phosphate buffer saline containing stabilizing protein and 0.05% Proclin 300
Specificity
The antibody can specifically recognize human CK13 protein.
Purification
The antibody was affinity-purified from ascites by affinity-chromatography using specific immunogen.
Storage
2°C to 8°C/1 year
Modification
Unmodified
Clonality
Monoclonal
Clone Number
ABT-CK13
Isotype
IgG1,Kappa
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Antigen&Target Information
Immunogen:
Synthesized peptide derived from human Cytokeratin 13 AA range: 400-458
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Specificity:
The antibody can specifically recognize human CK13 protein.
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Gene Name:
KRT13
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Protein Name:
Keratin, type I cytoskeletal 13 (Cytokeratin-13) (CK-13) (Keratin-13) (K13)
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Database Link:
Organism Gene ID SwissProt
Human 3860; P13646;
Background:
The protein encoded by this gene is a member of the keratin gene family. The keratins are intermediate filament proteins responsible for the structural integrity of epithelial cells and are subdivided into cytokeratins and hair keratins. Most of the type I cytokeratins consist of acidic proteins which are arranged in pairs of heterotypic keratin chains. This type I cytokeratin is paired with keratin 4 and expressed in the suprabasal layers of non-cornified stratified epithelia. Mutations in this gene and keratin 4 have been associated with the autosomal dominant disorder White Sponge Nevus. The type I cytokeratins are clustered in a region of chromosome 17q21.2. Alternative splicing of this gene results in multiple transcript variants; however, not all variants have been described. [provided by RefSeq, Jul 2008],
Function:
Disease:Defects in KRT13 are a cause of white sponge nevus of cannon (WSN) [MIM:193900]. WSN is a rare autosomal dominant disorder which predominantly affects non-cornified stratified squamous epithelia. Clinically, it is characterized by the presence of soft, white, and spongy plaques in the oral mucosa. The characteristic histopathologic features are epithelial thickening, parakeratosis, and vacuolization of the suprabasal layer of oral epithelial keratinocytes. Less frequently the mucous membranes of the nose, esophagus, genitalia and rectum are involved.,miscellaneous:There are two types of cytoskeletal and microfibrillar keratin: I (acidic; 40-55 kDa) and II (neutral to basic; 56-70 kDa).,online information:Keratin-13 entry,PTM:O-glycosylated; glycans consist of single N-acetylglucosamine residues.,similarity:Belongs to the intermediate filament family.,subunit:Heterotetramer of two type I and two type II keratins. keratin-13 is generally associated with keratin-4.,tissue specificity:Expressed in some epidermal sweat gland ducts (at protein level) and in exocervix, esophagus and placenta.,
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Cellular Localization:
Cytoplasmic, Membranous
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Tissue Expression:
Expressed in some epidermal sweat gland ducts (at protein level) and in exocervix, esophagus and placenta.
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Research Areas:
>>Estrogen signaling pathway ;
>>Staphylococcus aureus infection
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Catalog: YM6163R
Size
Price
Status
Qty.
10mL
$240.00
In stock

0

6mL
$180.00
In stock

0

3mL
$120.00
In stock

0

Add to cart

Collected

Collect

Customized Service

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