Background:

This gene is a member of the kelch-like family. The encoded protein contains a BACK domain| a BTB/POZ domain| and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM)| a rare congenital muscle disorder.

Classification:

Primary antibody

Alternative names:

KBTBA

Species reactivity:

Human, Rat

Host:

Rabbit

Isotype:

IgG

Immunogen:

Synthesized peptide derived from human KBTBA

Concentration:

1 mg/ml

Molecular weight:

66660

Applications:

WB

Storage:

-20°C for 1 year

More info:

Email: info@sobekbio.com

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