santa cruz biotechnology, inc.
SCBT Logo

환영 합니다!       장바구니에 품목이 있습니다.     빠른 구입

IFI-44 (N-18) Antibody (항체): sc-82937

 |  Datasheet (데이터 시트)
  • goat polyclonal IgG, 200µg/ml
  • epitope mapping at the N-terminus of IFI-44 of human origin
  • recommended for detection of IFI-44 of human origin by WB, IF and ELISA; non cross-reactive with other IFI family members
  • blocking peptide, sc-82937 P
 
다른 IFI 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 IFI44 10561 1p31.1 Q8TCB0
610468
 
통화

 주문정보
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
IFI-44 (N-18) sc-82937 200 µg/ml $279
IFI-44 (N-18) P sc-82937 P
(peptide)
100 µg/0.5 ml $61
 siRNA Gene Silencers (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
IFI-44 siRNA (h) sc-75320 10 µM $258
IFI-44 (h)-PR sc-75320-PR 10 µM $23
 shRNA Plasmids (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
IFI-44 shRNA Plasmid (h) sc-75320-SH 20 µg $520
 shRNA Lentiviral Particles (자세한 정보를 보시려면 제품명 클릭)
제품명카탈로그 번호 단위가격수량관심상품에 더하기즐겨찾기
IFI-44 shRNA (h) Lentiviral Particles sc-75320-V 200 µl $625

IFI-44 Background Information
The Interferon (IFN) family of proteins are able to alter the expression of a variety of target genes, thereby controlling a number of events within the cell. IFI-44 (interferon-induced protein 44), also known as p44 or MTAP44 (microtubule-associated protein 44), is a 444 amino acid protein that localizes to the cytoplasm and, upon induction by IFN-∫s, aggregates to form microtubular structures. Human IFI-44 shares 97% sequence similarity with its chimp counterpart, suggesting a conserved role between species. The gene encoding IFI-44 maps to human chromosome 1, which spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8% of the human genome. Chromosome 1 houses a large number of disease-associated genes, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson’s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.