Vergleich

Cytokeratin 2 [AE3]

ArtNr 20-272-191266
Hersteller GENWAY
Menge 0.1 ml
Kategorie
Typ Antibody
Applikationen WB, IHC
Clon AE3
Specific against other
ECLASS 10.1 32160702
ECLASS 11.0 32160702
UNSPSC 12352203
Alias GWB-DFC680
Similar products 20-272-191266
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Genway ID:
GWB-DFC680
Clone:
AE3
Isotype:
IgG1
Immunogen:
Human epidermal Keratins.
Antigen Species:
Human
Specificity:
This antibody is specific for all basic (type II) human keratins K1 K2 K3 K4 K5 K6 K7 and K8
Target:
Cytokeratin 2 Storage
Preservative:
0. 1% Sodium Azide; Constituents: PBS
Application Note:
Electron Microscopy: Use at an assay dependent dilution. IHC-P: Use at an assay dependent dilution. WB: Use at a dilution of 1/1000 - 1/3000. Use BSA (instead of milk which contains some keratins) to block nonspecific binding to immunoblots. Predicted
Molecular Weight:
56-70 kDa. Not tested in other applications. Optimal dilutions/concentrations should be determined by the end user. Myeloma: P3-X63 Ag8. 3
Function:
Probably contributes to terminal cornification. Associated with keratinocyte activation proliferation and keratinization.
Subunit:
Heterotetramer of two type I and two type II keratins. Associates with KRT10 (By similarity).
Tissue Specificity:
Expressed in the upper spinous and granular suprabasal layers of normal adult epidermal tissues from most body sites including thigh breast nipple foot sole penile shaft and axilla. Not present in foreskin squamous metaplasias and carcinomas. Expression in hypertrophic and keloid scars begins in the deepest suprabasal layer. Weakly expressed in normal gingiva and tongue however expression is induced in benign keratoses of lingual mucosa and in mild-to-moderate oral dysplasia with orthokeratinization. Developmental Stage: Synthesized during maturation of epidermal keratinocytes and localized in the upper intermediate cells of fetal skin. Earliest expression is at 10 weeks in the developing embryo in the presumptive nail bed of developing digits shifting to the proximal nail fold by 13. 5 weeks. At 12. 5 weeks detected in scattered cells of the intermediate layer of trunk skin. At 19. 3 weeks regional expression patterns were observed in upper intermediate keratinocytes of cheek trunk dorsal and ventral knee elbow and dorsal hand. Distal areas around the periumbilical region showed increased number of positive cells and by 15 weeks is expressed in small groups of cells in the fetal hair follicles.
Disease:
Defects in KRT2 are a cause of ichthyosis bullosa of Siemens (IBS) [MIM:146800]. IBS is a rare autosomal dominant skin disorder displaying a type of epidermolytic hyperkeratosis characterized by generalized erythema and extensive blistering from birth. Large dark gray hyperkeratoses are observed in later weeks. The skin of IBS patients is unusually fragile and has a tendency to shed the outer layers of the epidermis producing localized denuded areas (molting effect). IBS usually improves with age so that in most middle-aged patients the hyperkeratosis and keratotic lichenification is limited to the flexural folds of the major joints.
Miscellaneous:
There are two types of cytoskeletal and microfibrillar keratin: I (acidic; 40-55 kDa) and II (neutral to basic; 56-70 kDa).
Similarity:
Belongs to the intermediate filament family.

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Alle Produkte sind nur für Forschungszwecke bestimmt. Nicht für den menschlichen, tierärztlichen oder therapeutischen Gebrauch.

Menge: 0.1 ml
Lieferbar: In stock
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