santa cruz biotechnology, inc.
SCBT Logo

Benvenuto!       Visualizza carrello     Quick Order

XKRY (C-14) Anticorpo: sc-83952

 |  Scheda tecnica
  • rabbit polyclonal IgG, 100 µg/ml
  • epitope mapping near the C-terminus of XKRY of human origin
  • recommended for detection of XKRY of human origin by WB, IF and ELISA
  • blocking peptide, sc-83952 P
 
Altri XKR Anticorpi ...
 
Informazioni ordini
Recommended Support Products:
(click button of application of choice)
WB   IF   siRNA  
 
Specie Nome del gene Codice del gene Locus cromosoma Isoform (mRNA) Accession # codice accesso proteina Numero d'ordine
Umano XKRY 9082 Yq11.221 O14609
400015
 
Seleziona la valuta

 Informazioni ordini
Nome del prodottoCodice del prodottoUnitàPrezzoQuantitàAggiungiFavorites
XKRY (C-14) sc-83952 100 µg/ml $279
XKRY (C-14) P sc-83952 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gene Silencers (click product name for more information)
Nome del prodottoCodice del prodottoUnitàPrezzoQuantitàAggiungiFavorites
XKRY siRNA (h) sc-91541 10 µM $258
XKRY (h)-PR sc-91541-PR 10 µM $23
 shRNA plasmidi (click product name for more information)
Nome del prodottoCodice del prodottoUnitàPrezzoQuantitàAggiungiFavorites
XKRY shRNA Plasmid (h) sc-91541-SH 20 µg $520
 shRNA particelle lentivirali (click product name for more information)
Nome del prodottoCodice del prodottoUnitàPrezzoQuantitàAggiungiFavorites
XKRY shRNA (h) Lentiviral Particles sc-91541-V 200 µl $625

XKRY Background Information
XKRY (Kell blood group complex subunit-related, Y-linked), also known as testis-specific XK-related protein Y-linked, is a 159 amino acid protein belonging to the XK family. The gene that encodes XKRY is present as two identical copies within a palindromic and nonrecombining portion of the Y chromosome. The more centromeric copy of the XKRY gene is designated XKRY and the more telomeric copy is designated XKRY2. Localized to the plasma membrane, both XKRY and XKRY2 are expressed specifically in testis. XKRY and XKRY2 are similar to XK (X-linked Kell blood group precursor), a putative membrane transport protein that is associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems.