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PCP4L1 Antibodies

Santa Cruz Biotechnology, Inc. offers a broad range of PCP4L1 antibodies. Select PCP4L1 antibodies from several monoclonal and/or polyclonal PCP4L1 antibodies listed below. View detailed PCP4L1 antibody specifications by linking to the specific product blocks. Select appropriate PCP4L1 antibodies for your research by isotype, epitope, applications and species reactivity. PCP4L1 gene silencer products in siRNA, shRNA Plasmid and shRNA Lentiviral Particle formats are also available.

Introducing HOVERcruz™,

a unique system for rapid identification of PCP4L1 Antibodies. Hover over product names in the table to see representative data for each product.

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Our live chat system is available to answer your product and ordering questions.

PRODUCT NAMECAT. #ISOTYPEEPITOPEAPPLICATIONSSPECIESCITATIONSRATING
PCP4L1 (N-14)sc-241598goat IgGN-terminal (h)WB, IF, ELISAm, r, h

PCP4L1 siRNA, shRNA Plasmid and shRNA Lentiviral Particles gene silencers include:

siRNAsshRNA PlasmidsshRNA Lentiviral ParticlesCITATIONSRANKING
PCP4L1 siRNA (m): sc-152116PCP4L1 shRNA Plasmid (m):
sc-152116-SH
PCP4L1 shRNA (m)
Lentiviral Particles: sc-152116-V

PCP4L1 (purkinje cell protein 4-like protein 1), also known as IQM1, is a 68 amino acid protein that contains one IQ domain and belongs to the PCP4 family. The gene that encodes PCP4L1 consists of approximately 26,724 bases and maps to human chromosome 1q23.3. Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8% of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1.