Thermo Fisher Scientific SQSTM1 Monoclonal Antibody (GT1478)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
MA527800 | - | Thermo Fisher Scientific MA527800 SQSTM1 Monoclonal Antibody (GT1478) 100 ul pk | 재고문의 | pk | 733,000원 | - | 806,300원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
1:500-1:3,000
View 3 publications 3 publications
Immunohistochemistry (Frozen) (IHC (F))
1:100-1:1,000
Immunocytochemistry (ICC/IF)
1:100-1:1,000
View 1 publication 1 publication
Flow Cytometry (Flow)
1:50-1:200
Product Specifications
Species Reactivity
Human, Mouse
Published species
Human, Mouse
Host/Isotype
Mouse / IgG2b
Class
Monoclonal
Type
Antibody
Clone
GT1478
Immunogen
Recombinant protein encompassing a sequence within the center region of human SQSTM1. The exact sequence is proprietary.
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Purification
Protein G
Storage buffer
PBS, pH 7, with 20% glycerol
Contains
no preservative
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2735371
Product Specific Information
Positive Control: HepG2, A549, H1299, HCT116, Huh-7 (untreated), Huh-7 (3 µM Thapsigargin treatment for 12 hr), Huh-7 (3 µM Thapsigargin treatment for 24 hr), HepG2 (3 µM Thapsigargin treatment for 12 hr), HepG2 (3 µM Thapsigargin treatment for 24 hr), 2C4, MEF, MNT-1
Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.
Target Information
This gene encodes a multifunctional protein that binds ubiquitin and regulates activation of the nuclear factor kappa-B signaling pathway. The protein functions as a scaffolding/adaptor protein in concert with TNF receptor-associated factor 6 to mediate activation of NF-kB in response to upstream signals. Alternatively spliced transcript variants encoding either the same or different isoforms have been identified for this gene. Mutations in this gene result in sporadic and familial Paget disease of bone.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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