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BAALC (A-14) Antibody: sc-70020

 |  Datasheet
  • goat polyclonal IgG, 200µg/ml
  • epitope mapping within an internal region of BAALC of human origin
  • recommended for detection of BAALC of mouse, rat and human origin by ELISA; also reactive with additional species, including bovine and porcine
  • blocking peptide, sc-70020 P
 
Additional BAALC Antibodies ...
 
Ordering Information
 
Species Gene Name Gene ID Chromosome Location Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human BAALC 79870 8q22.3 Q8WXS3
606602
 
Set Currency

 Ordering Information
Product NameCatalog #UnitPriceQtyAddFavorites
BAALC (A-14) sc-70020 200 µg/ml $279
BAALC (A-14) P sc-70020 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
BAALC siRNA (h) sc-72595 10 µM $258
BAALC siRNA (m) sc-72596 10 µM $258
BAALC (h)-PR sc-72595-PR 10 µM $23
BAALC (m)-PR sc-72596-PR 10 µM $23
 shRNA Plasmids (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
BAALC shRNA Plasmid (h) sc-72595-SH 20 µg $520
BAALC shRNA Plasmid (m) sc-72596-SH 20 µg $520
 shRNA Lentiviral Particles (click product name for more information)
Product NameCatalog #UnitPriceQtyAddFavorites
BAALC shRNA (h) Lentiviral Particles sc-72595-V 200 µl $625
BAALC shRNA (m) Lentiviral Particles sc-72596-V 200 µl $625

BAALC Background Information
BAALC (brain and acute leukemia, cytoplasmic) is a 180 amino acid protein that localizes to both the membrane and the cytoplasm and exists as multiple alternatively spliced isoforms. Expressed by hematopoetic and neural cells, BAALC interacts with CaMKIIå and is thought to play a role in synaptic function at postsynaptic lipid rafts. BAALC may be overexpressed in acute myeloid leukemia (AML), suggesting a role in tumorigenesis. The gene encoding BAALC maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that maps to chromosome 8.