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Thermo Fisher Scientific FAM111A Polyclonal Antibody
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Thermo Fisher Scientific FAM111A Polyclonal Antibody

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FAM111A 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot에 적합하며 Human, Mouse, Rat 반응성. 높은 순도(>95%)로 항원 친화 크로마토그래피 정제. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 03. 오전 01:55
Thermo Fisher Scientific PA575167 FAM111A Polyclonal Antibody 100 ul pk판매 단위 pk ·
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642,300원VAT 포함 706,530원

Thermo Fisher Scientific · Thermo Fisher Scientific FAM111A Polyclonal Antibody

Thermo Fisher Scientific FAM111A Polyclonal Antibody

Applications

  • Western Blot (WB): 1:500–1:1,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide corresponding to residues in Human FAM111A
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
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_2718895

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using an epitope-specific immunogen, and the purity is >95% (by SDS-PAGE).

Target Information

Chromosome 11 comprises approximately 135 million base pairs and 1,400 genes, accounting for about 4% of human genomic DNA. It is considered a gene- and disease-association dense chromosome.
The chromosome 11 encoded Atm gene regulates cell cycle arrest and apoptosis following double-strand DNA breaks; mutations lead to ataxia telangiectasia.
Blood disorders such as sickle cell anemia and β-thalassemia arise from HBB gene mutations.
Wilms' tumors, WAGR syndrome, and Denys-Drash syndrome are linked to WT1 gene mutations.
Other disorders associated with chromosome 11 defects include Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome.
The FAM111A gene product has been provisionally designated FAM111A pending further characterization.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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