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JAGN1 (N-19) Antibody (항체): sc-102629

 |  Datasheet (데이터 시트)
  • rabbit polyclonal IgG, 100µg/ml
  • epitope mapping near the N-terminus of JAGN1 of human origin
  • recommended for detection of JAGN1 of mouse and human origin by WB, IF and ELISA; also reactive with additional species, including equine, canine, bovine and porcine
  • blocking peptide, sc-102629 P
 
다른 JAGN1 Antibodies (항체) ...
 
주문정보
추천하는 보조제품:
원하시는 application에 클릭해 주세요.
WB   IF   siRNA  
 
Species 유전자 이름 (Gene Name) 유전자 ID 염색체 위치 Isoform (mRNA) Accession # Protein Accession # OMIM™ Number
Human JAGN1 84522 3p25.3 Q8N5M9
n/a
 
통화

 주문정보
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
JAGN1 (N-19) sc-102629 100 µg/ml $279
JAGN1 (N-19) P sc-102629 P
(peptide)
100 µg/0.5ml $61
 siRNA Gene Silencers (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
JAGN1 siRNA (h) sc-78313 10 µM $258
JAGN1 siRNA (m) sc-146316 10 µM $258
JAGN1 (h)-PR sc-78313-PR 10 µM $23
JAGN1 (m)-PR sc-146316-PR 10 µM $23
 shRNA Plasmids (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
JAGN1 shRNA Plasmid (h) sc-78313-SH 20 µg $520
JAGN1 shRNA Plasmid (m) sc-146316-SH 20 µg $520
 shRNA Lentiviral Particles (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
JAGN1 shRNA (h) Lentiviral Particles sc-78313-V 200 µl $625
JAGN1 shRNA (m) Lentiviral Particles sc-146316-V 200 µl $625
 WB Positive Control Cell Lysate (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
Jurkat Whole Cell Lysate sc-2204 500 µg/200 µl $104

JAGN1 Background Information
The gene encoding JAGN1, a 183 amino acid protein, maps to human chromosome 3. Chromosome 3 is made up of about 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.