Rabbit Polyclonal Anti-TGFbeta3 antibody (STJ98771)


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

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Rabbit Polyclonal Anti-TGFbeta3 antibody (STJ98771)

Supplier: St John’s Laboratory Ltd.

Recommended applications: IHC-P, ELISA

Recommended dilution: IHC-P 1:50-300; ELISA 1:5000-20000

Recommended protocols: check protocols

Image descriptions:

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Alternative names:

Check alternative names for the antibody


|ARVD antibody|ARVD1 antibody|FLJ16571 antibody|LDS5 antibody|MGC105479 antibody|MGC118722 antibody|prepro-transforming growth factor beta-3 antibody|RNHF antibody|TGF beta 3 antibody|TGF beta3 antibody|TGF-beta-3 antibody|TGFB 3 antibody|Tgfb3 antibody|TGFB3_HUMAN antibody|transforming growth factor beta 3 antibody|Transforming growth factor beta-3 antibody|Anti-TGF beta antibody (ab66043)
SCBT cat No: sc-80151|sc-34830|sc-160486|sc-81610|sc-19784|sc-28541|sc-19783|sc-376270|sc-398601|sc-271958|sc-514618|sc-365462|


Anti-TGFbeta3 antibody

Catalogue No.



Human, Mouse, Rat


Anti-TGFbeta3 antibody detects endogenous TGFbeta3.


Synthetic peptide from human protein at AA range: 221-270.












Anti-TGFbeta3 antibody was tube-contained in PBS, pH 7.4, containing 0.02% sodium azide as Preservative and 50% Glycerol.


1 mg/ml


Anti-TGFbeta3 antibody was affinity-purified from rabbit serum by affinity-chromatography using specific immunogen.


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

Alternative antibody names

ARVD antibody, ARVD1 antibody, FLJ16571 antibody, LDS5 antibody, MGC105479 antibody, MGC118722 antibody, prepro-transforming growth factor beta-3 antibody, RNHF antibody, TGF beta 3 antibody, TGF beta3 antibody, TGF-beta-3 antibody, TGFB 3 antibody, Tgfb3 antibody, TGFB3_HUMAN antibody, transforming growth factor beta 3 antibody, Transforming growth factor beta-3 antibody

Protein function

Involved in embryogenesis and cell differentiation.

Involvement in disease

Arrhythmogenic right ventricular dysplasia, familial, 1 (ARVD1) [MIM:107970]: A congenital heart disease characterized by infiltration of adipose and fibrous tissue into the right ventricle and loss of myocardial cells, resulting in ventricular and supraventricular arrhythmias. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Loeys-Dietz syndrome 5 (LDS5) [MIM:615582]: A form of Loeys-Dietz syndrome, a syndrome with widespread systemic involvement characterized by arterial tortuosity and aneurysms, hypertelorism, and bifid uvula or cleft palate. LDS5 additional variable features include mitral valve disease, skeletal overgrowth, cervical spine instability, and clubfoot deformity. LDS5 patients do not manifest remarkable aortic or arterial tortuosity, and there is no strong evidence for early aortic dissection. . Note=The disease is caused by mutations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the TGF-beta family.

Protein post-translational modifications

The precursor is cleaved into mature TGF-beta-3 and LAP, which remains non-covalently linked to mature TGF-beta-3 rendering it inactive. .

Protein cellular localization



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St John’s Laboratory Ltd.

Product type

Primary antibody


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