"SPG11" Related Products

Recombinant Human SPG11 cell lysate

Cat.No.: SPG11-1681HCL
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 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;

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