Cytokeratin 17 rabbit pAb

Cytokeratin 17 rabbit pAb

AO-06-ES2127-50

Cytokeratin 17 rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES2127
Product nameCytokeratin 17 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;IHC;IF;ELISA
Other nameKRT17; Keratin; type I cytoskeletal 17; 39.1; Cytokeratin-17; CK-17; Keratin-17; K17
Size50μL
Unit price ($)148
Human gene ID3872
Human Swiss-ProtQ04695
SourceRabbit
IsotypeIgG
TargetCytokeratin 17
Fields>>Estrogen signaling pathway;>>Staphylococcus aureus infection
Gene nameKRT17
Protein nameKeratin type I cytoskeletal 17
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID16667
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtQ9QWL7
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID287702
Rat gene linkView Rat Gene
Rat Swiss-ProtQ6IFU8
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human Keratin 17. AA range:381-430
SpecificityCytokeratin 17 Polyclonal Antibody detects endogenous levels of Cytokeratin 17 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. Immunofluorescence: 1/200 - 1/1000. ELISA: 1/20000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)48kD
BackgroundThis gene encodes the type I intermediate filament chain keratin 17, expressed in nail bed, hair follicle, sebaceous glands, and other epidermal appendages. Mutations in this gene lead to Jackson-Lawler type pachyonychia congenita and steatocystoma multiplex. [provided by RefSeq, Aug 2008],
Functiondisease:Defects in KRT17 are a cause of pachyonychia congenita type 2 (PC2) [MIM:167210]; also known as pachyonychia congenita Jackson-Lawler type. PC2 is an autosomal dominant ectodermal dysplasia characterized by hypertrophic nail dystrophy resulting in onchyogryposis (thickening and increase in curvature of the nail), palmoplantar keratoderma and hyperhidrosis, follicular hyperkeratosis, multiple epidermal cysts, absent/sparse eyebrow and body hair, and by the presence of natal teeth.,disease:Defects in KRT17 are a cause of steatocystoma multiplex (SM) [MIM:184500]. SM is a disease characterized by round or oval cystic tumors widely distributed on the back, anterior trunk, arms, scrotum, and thighs.,disease:KRT16 and KRT17 are coexpressed only in pathological situations such as metaplasias and carcinomas of the uterine cervix and in psoriasis vulgaris.,function:May play a role in the
Subcellular locationCytoplasm .
ExpressionExpressed in the outer root sheath and medulla region of hair follicle specifically from eyebrow and beard, digital pulp, nail matrix and nail bed epithelium, mucosal stratified squamous epithelia and in basal cells of oral epithelium, palmoplantar epidermis and sweat and mammary glands. Also expressed in myoepithelium of prostate, basal layer of urinary bladder, cambial cells of sebaceous gland and in exocervix (at protein level).

Additional Images

Image 1
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Western Blot analysis of various cells using Cytokeratin 17 Polyclonal Antibody diluted at 1:2000
Image 2
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Immunofluorescence analysis of HepG2 cells, using Keratin 17 Antibody. The picture on the right is blocked with the synthesized peptide.
Image 3
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Immunohistochemistry analysis of paraffin-embedded human breast carcinoma tissue, using Keratin 17 Antibody. The picture on the right is blocked with the synthesized peptide.
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Western blot analysis of lysates from HUVEC cells, using Keratin 17 Antibody. The lane on the right is blocked with the synthesized peptide.
: AO-06-ES2127-50
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