Mouse Monoclonal p63 antibody [4E5] (STJ98303)

$379.00

Reactivity: Human, Mouse, Rat, Monkey
Applications: WB, IHC, ELISA
Conjugation: Unconjugated
Supplier: St John’s Laboratory Ltd.

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Mouse Monoclonal p63 antibody [4E5] (STJ98303)

Supplier: St John’s Laboratory Ltd.

Recommended applications: WB, IHC, ELISA

Recommended dilution: WB 1:500-1:2000; IHC 1:200-1:1000; ELISA 1:10000

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody

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SCBT cat No: To be updated

 

Name

p63 Monoclonal Antibody

Catalogue No.

STJ98303

Reactivity

Human, Mouse, Rat, Monkey

Specificity

p63 Monoclonal Antibody detects endogenous levels of p63 protein.

Immunogen

Synthesized peptide of human p63

Host

Mouse

Applications

WB, IHC, ELISA

Recommended dilution

WB 1:500-1:2000; IHC 1:200-1:1000; ELISA 1:10000

Clonality

Monoclonal

Conjugation

Unconjugated

Isotype

IgG1

Formulation

p63 Antibody was tube-contained. Ascitic fluid containing 0.03% sodium azide.

Concentration

1 mg/ml

Purification

p63 Antibody was purified using affinity purification.

Storage

-20 Celsius degree. Avoid repeated freeze/thaw cycles.

Alternative antibody names

Tumor protein 63 antibody, p63 antibody, Chronic ulcerative stomatitis protein antibody, CUSP antibody, Keratinocyte transcription factor KET antibody, Transformation-related protein 63 antibody, TP63 antibody, Tumor protein p73-like antibody, p73L antibody, p40 antibody, p51 antibody

Database links

Human UniProt/Swiss-Prot:Q9H3D4;Mouse UniPort/Swiss-Prot: O88898;Rat UniProt/Swiss-Port: Q9JJP6;Human Entrez Gene: 8626;Mouse Entrez Gene: 22061;Rat Entrez Gene: Rn.42907

Protein names

Tumor protein 63 , p63 , Chronic ulcerative stomatitis protein , CUSP , Keratinocyte transcription factor KET , Transformation-related protein 63 , TP63 , Tumor protein p73-like , p73L , p40 , p51

Involvement in disease

Acro-dermato-ungual-lacrimal-tooth syndrome (ADULT syndrome) [MIM:103285]: A form of ectodermal dysplasia. Ectodermal dysplasia defines a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. ADULT syndrome involves ectrodactyly, syndactyly, finger- and toenail dysplasia, hypoplastic breasts and nipples, intensive freckling, lacrimal duct atresia, frontal alopecia, primary hypodontia and loss of permanent teeth. ADULT syndrome differs significantly from EEC3 syndrome by the absence of facial clefting. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Ankyloblepharon-ectodermal defects-cleft lip/palate (AEC) [MIM:106260]: An autosomal dominant condition characterized by congenital ectodermal dysplasia with coarse, wiry, sparse hair, dystrophic nails, slight hypohidrosis, scalp infections, ankyloblepharon filiform adnatum, maxillary hypoplasia, hypodontia and cleft lip/palate. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3) [MIM:604292]: A form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. It is an autosomal dominant syndrome characterized by ectrodactyly of hands and feet, ectodermal dysplasia and facial clefting. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Split-hand/foot malformation 4 (SHFM4) [MIM:605289]: A limb malformation involving the central rays of the autopod and presenting with syndactyly, median clefts of the hands and feet, and aplasia and/or hypoplasia of the phalanges, metacarpals, and metatarsals. Some patients have been found to have mental retardation, ectodermal and craniofacial findings, and orofacial clefting. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Limb-mammary syndrome (LMS) [MIM:603543]: Characterized by ectrodactyly, cleft palate and mammary-gland abnormalities. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Note: Defects in TP63 are a cause of cervical, colon, head and neck, lung and ovarian cancers.; Ectodermal dysplasia, Rapp-Hodgkin type (EDRH) [MIM:129400]: A form of ectodermal dysplasia, a heterogeneous group of disorders due to abnormal development of two or more ectodermal structures. Characterized by the combination of anhidrotic ectodermal dysplasia, cleft lip, and cleft palate. The clinical syndrome is comprised of a characteristic facies (narrow nose and small mouth), wiry, slow-growing, and uncombable hair, sparse eyelashes and eyebrows, obstructed lacrimal puncta/epiphora, bilateral stenosis of external auditory canals, microsomia, hypodontia, cone-shaped incisors, enamel hypoplasia, dystrophic nails, and cleft lip/cleft palate. . Note: The disease is caused by mutations affecting the gene represented in this entry.; Non-syndromic orofacial cleft 8 (OFC8) [MIM:129400]: A birth defect consisting of cleft lips with or without cleft palate. Cleft lips are associated with cleft palate in two-third of cases. A cleft lip can occur on one or both sides and range in severity from a simple notch in the upper lip to a complete opening in the lip extending into the floor of the nostril and involving the upper gum. Note: The disease is caused by mutations affecting the gene represented in this entry.

Research area

All research areas>Transcription Regulators>TAF Basal Transcription Factor
(View all antibody categories related to Transcription Regulators)

Note

AntibodyPlus can customize p63 Antibody according to your requirement, including bulk product size,etc. Please contact info@antibodyplus.com. AntibodyPlus provide antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

St John’s Laboratory Ltd.

Product type

Primary antibody

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