Anti-TCOF1 Antibody

$99.00$319.00

Reactivity: Human
Applications: ELISA,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-TCOF1 Antibody (CSB-PA619765DSR2HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

Treacher Collins syndrome protein Antibody,TCOF1 Antibody

More alternative names for the antibody
Mandibulofacial dysostosis antibody|MFD1 antibody|Nucleolar trafficking phosphoprotein antibody|TCOF 1 antibody|TCOF_HUMAN antibody|TCOF1 antibody|TCS antibody|TCS1 antibody|Treacher Collins Franceschetti syndrome 1 antibody|Treacher Collins syndrome antibody|Treacher Collins syndrome protein antibody|Treacle antibody|Treacle protein antibody
Anti-Treacher Collins syndrome protein antibody – ChIP Grade (ab65212)
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Recommended applications: ELISA, IHC

Recommended dilution: Recommended dilution:IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-TCOF1 Antibody

Catalogue No.

CSB-PA619765DSR2HU

Reactivity

Human

Immunogen

Recombinant human Treacle protein (1189-1488AA)

Host

Rabbit

Applications

ELISA, IHC

Recommended dilution

Recommended dilution:IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

152 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:6949( Human), Entrez Gene:21453( Mouse), Omim:154500( Human), SwissProt:Q13428( Human), SwissProt:O08784( Mouse), Unigene:519672( Human), Unigene:605019( Human), Unigene:2215( Mouse)

Protein function

May be involved in nucleolar-cytoplasmic transport. May play a fundamental role in early embryonic development, particularly in development of the craniofacial complex (By similarity). May participate in certain stages of ribosome biogenesis. .

Involvement in disease

Treacher Collins syndrome 1 (TCS1) [MIM:154500]: A form of Treacher Collins syndrome, a disorder of craniofacial development. Treacher Collins syndrome is characterized by a combination of bilateral downward slanting of the palpebral fissures, colobomas of the lower eyelids with a paucity of eyelashes medial to the defect, hypoplasia of the facial bones, cleft palate, malformation of the external ears, atresia of the external auditory canals, and bilateral conductive hearing loss. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein cellular localization

Nucleus, nucleolus .

Research area

All research areas>Transcription Regulators>Treacle
(View all antibody categories related to Transcription Regulators)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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