Descrizione Azione

The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts witHuman, Mouseany other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Codice: E-AB-13234_20μL Confezionamento: 20μL
Dettagli

The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts witHuman, Mouseany other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Codice: E-AB-13234_60μL Confezionamento: 60μL
Dettagli

The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts witHuman, Mouseany other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Codice: E-AB-13234_120μL Confezionamento: 120μL
Dettagli

The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts witHuman, Mouseany other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Codice: E-AB-16424_20μL Confezionamento: 20μL
Dettagli

The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts witHuman, Mouseany other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Codice: E-AB-16424_200μL Confezionamento: 200μL
Dettagli

The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts witHuman, Mouseany other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Codice: E-AB-16424_120μL Confezionamento: 120μL
Dettagli

The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts witHuman, Mouseany other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).

Codice: E-AB-16424_60μL Confezionamento: 60μL
Dettagli

A synthesized peptide derived from human AMFR, corresponding to a region within the internal amino acids.

Codice: DF7718 Confezionamento: 100ul
Dettagli

A synthesized peptide derived from human AMH, corresponding to a region within C-terminal amino acids.

Codice: DF13527 Confezionamento: 100ul
Dettagli

Anti-Mullerian hormone is a member of the transforming growth factor-beta gene family which mediates male sexual differentiation. Anti-Mullerian hormone causes the regression of Mullerian ducts which would otherwise differentiate into the uterus and fallopian tubes. Some mutations in the anti-Mullerian hormone result in persistent Mullerian duct syndrome.

Codice: AN200148P_100μL Confezionamento: 100μL
Dettagli
Codice: A54922-100 Confezionamento: 100 µl
Dettagli
Codice: A54922-100 Confezionamento: 100 µl
Dettagli