WHRN

Deafness, autosomal recessive 31

DFNB31 is thought to function in the organization and stabilization of sterocilia elongation and actin cystoskeletal assembly, based on studies of the related mouse gene. Mutations in this gene have been associated with autosomal recessive non-syndromic deafness and Usher Syndrome. Alternative splicing of this gene results in multiple transcript variants encoding different isoforms.

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Proteins (3)

Type

Over-Expression Lysate (2)

Recombinant (1)

Target

WHRN (3)

Publications

No (3)

Tag

GST (1)

Myc-DDK (Flag) (2)

Species

Human (2)

Source

293T Cells (1)

HEK 293 Cells (1)

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Human WHRN Protein (Recombinant GST) - LS-G132159

Tag:

GST

Molecular Weight:

36.74kDa

Price:

10 µg/$479; 25 µg/$670

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WHRN Protein (Over-Expression Lysate Myc-DDK (Flag)) (Full Length) - LS-G113241

Source:

HEK 293 Cells

Tag:

Myc-DDK (Flag)

Molecular Weight:

96.4 kDa

Price:

100 µg/$710

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Human WHRN Protein (Over-Expression Lysate Myc-DDK (Flag)) (Full Length) - LS-G94449

Source:

293T Cells

Tag:

Myc-DDK (Flag)

Molecular Weight:

96.4 kDa

Price:

20 µg/$215

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