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Thermo Fisher Scientific PABPN1 Recombinant Rabbit Monoclonal Antibody (ARC0730)
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Thermo Fisher Scientific PABPN1 Recombinant Rabbit Monoclonal Antibody (ARC0730)

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PABPN1 단백질을 인식하는 토끼 리콤비넌트 단클론 항체. Western blot, IHC, ICC/IF, ELISA에 적합. 인간, 마우스, 랫트 반응성. HEK293 발현, Affinity Chromatography 정제. -20°C 보관, 연구용 전용.

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MA535184
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오후 12:10
Thermo Fisher Scientific MA535184 PABPN1 Recombinant Rabbit Monoclonal Antibody (ARC0730) 100 ul pk판매 단위 pk ·
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598,300원VAT 포함 658,130원

Thermo Fisher Scientific · Thermo Fisher Scientific PABPN1 Recombinant Rabbit Monoclonal Antibody (ARC0730)

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:1,000–1:6,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:2,000
Immunocytochemistry (ICC/IF) 1:200–1:2,000
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone ARC0730
Immunogen Synthetic peptide corresponding to amino acids 1–100 of human PABPN1 (Q86U42)
Conjugate Unconjugated
Form Liquid
Concentration 0.19 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol, 0.05% BSA
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2849089

Product Specific Information

Immunogen sequence:
MAAAAAAAAA AGAAGGRGSG PGRRRHLVPG AGGEAGEGAP GGAGDYGNGL ESEELEPEEL LLEPEPEPEP EEEPPRPRAP PGAPGPGPGS GAPGSQEEEE


Target Information

This gene encodes an abundant nuclear protein that binds with high affinity to nascent poly(A) tails. It is required for progressive and efficient polymerization of poly(A) tails at the 3′ ends of eukaryotic transcripts and controls the size of the poly(A) tail (~250 nt). At steady-state, this protein is localized in the nucleus, whereas a different poly(A) binding protein is localized in the cytoplasm. Expansion of the GCG trinucleotide repeat (normally 6 copies to 8–13 copies) leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD). Related pseudogenes exist on chromosomes 19 and X, and read-through transcription occurs with the neighboring BCL2L2 gene.


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

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