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GOLPH3 Antibodies

Santa Cruz Biotechnology, Inc. offers a broad range of gene silencers in the form of siRNAs, shRNA Plasmids and shRNA Lentiviral Particles. GOLPH3 gene silencers are available as GOLPH3 siRNA, GOLPH3 shRNA Plasmid and GOLPH3 shRNA Lentiviral Particles. Gene silencers are useful for gene studies in combination with antibodies used for protein detection.

Introducing HOVERcruz™,

a unique system for rapid identification of GOLPH3 Antibodies. Hover over product names in the table to see representative data for each product.

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PRODUCT NAMECAT. #ISOTYPEEPITOPEAPPLICATIONSSPECIESCITATIONSRATING
GOLPH3L (N-18)sc-242931goat IgGN-terminal (h)WB, IF, ELISAhuman

GOLPH3 siRNA, shRNA Plasmid and shRNA Lentiviral Particles gene silencers include:

siRNAsshRNA PlasmidsshRNA Lentiviral ParticlesCITATIONSRANKING
GOLPH3 siRNA (h): sc-91952GOLPH3 shRNA Plasmid (h):
sc-91952-SH
GOLPH3 shRNA (h)
Lentiviral Particles: sc-91952-V
GOLPH3 siRNA (m): sc-145671GOLPH3 shRNA Plasmid (m):
sc-145671-SH
GOLPH3 shRNA (m)
Lentiviral Particles: sc-145671-V
GOLPH3 siRNA (r): sc-270270GOLPH3 shRNA Plasmid (r):
sc-270270-SH
GOLPH3 shRNA (r)
Lentiviral Particles: sc-270270-V
GOLPH3L siRNA (h): sc-88799GOLPH3L shRNA Plasmid (h):
sc-88799-SH
GOLPH3L shRNA (h)
Lentiviral Particles: sc-88799-V
GOLPH3L siRNA (m): sc-145672GOLPH3L shRNA Plasmid (m):
sc-145672-SH
GOLPH3L shRNA (m)
Lentiviral Particles: sc-145672-V

The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. GOLPH3L (golgi phosphoprotein 3-like), also known as GPP34R, is a 285 amino acid cytoplasmic protein that localizes to the Golgi apparatus. Belonging to the GOLPH3/VPS74 family, GOLPH3L may have a regulatory role in Golgi trafficking. GOLPH3L is encoded by a gene located on human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.