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BAT9 (S-16) Antikörper: sc-167178

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  • goat polyclonal IgG, 200 µg/ml
  • epitope mapping within an internal region of BAT9 of human origin
  • recommended for detection of BAT9 of mouse, rat and human origin by WB, IF and ELISA; non cross-reactive with other BAT family members
  • blocking peptide, sc-167178 P
 
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WB   IF  
 
Spezies Gen Gen ID Chromosomaler Locus mRNA (Isoform) Accession # Protein Accession # OMIM™ Nummer
Human ZBTB12 221527 6p21.33 NM_181842 Q9Y330
n/a
Maus Zbtb12 193736 17 B1 NM_198886 NP_942589
n.n.
 
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ProduktKatalog #MengePreisAnzahlKaufFavorit
BAT9 (S-16) sc-167178 200 µg/ml $279
BAT9 (S-16) P sc-167178 P
(peptide)
100 µg/0.5 ml $61

BAT9 Background Information
BAT9, also known as Protein G10 or ZBTB12 (zinc finger and BTB domain containing 12), is a 459 amino acid protein that may be involved in transcriptional regulation. BAT9 localizes to nucleus, contains one BTB (POZ) domain and four C2H2-type zinc fingers. The BAT9 gene maps to human chromosome 6p21.32. Making up nearly 6% of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6.