Recombinant Human SPG11 cell lysate

• Cat.No.: SPG11-1681HCL

Specification

• Description: The protein encoded by this gene is a potential transmembrane protein that is phosphorylated upon DNA damage. Defects in this gene are a cause of spastic paraplegia type 11 (SPG11). Multiple transcript variants encoding different isoforms have been found for this gene.
• Species: Human
• Size: 100 ul
• Storage Buffer: 1X Sample Buffer (50 mM Tris-HCl, 2% SDS, 10% glycerol, 300 mM 2-mercaptoethanol, 0.01% Bromophenol blue)
• Applications: Western Blot

Gene Information

• Gene Name: SPG11 spastic paraplegia 11 (autosomal recessive) [ Homo sapiens ]
• Official Symbol: SPG11
• Synonyms: SPG11; spastic paraplegia 11 (autosomal recessive); KIAA1840; spatacsin; FLJ21439; spastic paraplegia 11 protein; colorectal carcinoma-associated protein; DKFZp762B1512
• Gene ID: 80208
• mRNA Refseq: NM_001160227
• Protein Refseq: NP_001153699
• MIM: 610844
• UniProt ID: Q96JI7
• Chromosome Location: 15q13-q15
• Function: protein binding