HSPB7 Polyclonal Antibody, 50ul Liquid Handling ＆Storage Mutations in the gene are

Mutations in the gene are known to cause autosomal recessive hypophosphatemia

and is a member of the sodium:neurotransmitter symporter family

A nuclear localization signal (NLS) is present at the amino terminal end of the nuclear form but is lacking in the cytoplasmic form due to use of an alternate translation start codon

Multiple transcript variants encoding different protein isoforms were identified through sequence analysis

which in turn plays a role in myelination

HSPB7 Polyclonal Antibody, 50ul Liquid Handling ＆Storage Mutations in the gene areBelongs to the small heat shock protein (HSP20) family.,subunit: Interacts with C terminal domain of actin binding protein 280.,tissue specificity: Isoform 1 is highly expressed in adult and fetal heart, skeletal muscle, and at a much lower levels in adipose tissue and in aorta. Undetectable in other tissues. Isoform 2 and isoform 3 are poorly detected in heart.,