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VCPIP1 (N-12) Antibody (항체): sc-98199

 |  Datasheet (데이터 시트)
  • rabbit polyclonal IgG, 100µg/ml
  • epitope mapping near the N-terminus of VCPIP1 of human origin
  • recommended for detection of VCPIP1 of mouse, rat and human origin by WB, IF and ELISA; also reactive with additional species, including equine, canine, bovine, porcine and avian
  • blocking peptide, sc-98199 P
 
다른 VCPIP 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 VCPIP1 80124 8q13.1 Q96JH7
611745
 
통화

 주문정보
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
VCPIP1 (N-12) sc-98199 100 µg/ml $279
VCPIP1 (N-12) P sc-98199 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gene Silencers (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
VCPIP1 siRNA (h) sc-77549 10 µM $258
VCPIP1 siRNA (m) sc-155098 10 µM $258
VCPIP1 (h)-PR sc-77549-PR 10 µM $23
VCPIP1 (m)-PR sc-155098-PR 10 µM $23
 shRNA Plasmids (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
VCPIP1 shRNA Plasmid (h) sc-77549-SH 20 µg $520
VCPIP1 shRNA Plasmid (m) sc-155098-SH 20 µg $520
 shRNA Lentiviral Particles (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
VCPIP1 shRNA (h) Lentiviral Particles sc-77549-V 200 µl $625
VCPIP1 shRNA (m) Lentiviral Particles sc-155098-V 200 µl $625

VCPIP1 Background Information
VCPIP1 (valosin containing protein (p97)/p47 complex interacting protein 1), also known as DUBA3 or VCIP135, is a 1,222 amino acid protein that contains one OTU domain and localizes to the endoplasmic reticulum (ER), as well as to golgi stacks within the golgi apparatus. Interacting with VCP (valosin-containing protein) and p47, VCPIP1 functions as a deubiquitinating enzyme that is necessary for post-mitotic golgi stack formation and may also play a role in the VCP-mediated creation of the transitional ER (tER). The gene encoding VCPIP1 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.