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FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02609] Electronic Pipette Translocation t(11|19)(q21|p13) with MAML2

SKU: 36675909283

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FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02609] Electronic Pipette Translocation t(11|19)(q21|p13) with MAML2disease: Defects in F8 are the cause of hemophilia A (HEMA)

Store: humanprojects.de · Domain: humanprojects.de

Description

Translocation t(11|19)(q21|p13) with MAML2

Mutations in this gene are associated with Leigh syndrome resulting from mitochondrial complex I deficiency

Neuronal PAS domain-containing protein 2 encoded by NPAS2 is a member of the basic helix-loop-helix (bHLH)-PAS family of transcription factors

Both SSF1 and ppan are essential for cell growth and proliferation

with 1 rxn/μl

FA8A Rabbit Polyclonal Antibody, 50ul[BT-AP02609] Electronic Pipette Translocation t(11|19)(q21|p13) with MAML2disease: Defects in F8 are the cause of hemophilia A (HEMA)

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