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Thermo Fisher Scientific PABPN1 Polyclonal Antibody
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Thermo Fisher Scientific PABPN1 Polyclonal Antibody

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PABPN1 단백질을 인식하는 Thermo Fisher Scientific의 폴리클로날 항체로, Western blot 및 IHC(P) 검증 완료. 인간 및 마우스 반응성. 항원 친화 크로마토그래피 정제, 액상 형태, 장기 보관 시 -20°C 권장. 연구용 전용 제품.

카탈로그번호
PA551430
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 06:43
Thermo Fisher Scientific PA551430 PABPN1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific PABPN1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution Publications
Western Blot (WB) 0.04–0.4 µg/mL View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Mouse
Published Species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human Bcl-W. Recombinant protein control fragment (Product #RP-88906)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% 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 Wet ice
RRID AB_2638516

Product Specific Information

Immunogen sequence:
MSIEEKMEAD ARSIYVGNVD YGATAEELEA HFHGCGSVNR VTILCDKFSG HPKGFAYIEF SDKESVRTSL ALDESLFRGR QIKVIPKRTN RPGISTTDRG FPRARYRART TNYNSSRSRF YSGFNSRPRG RVYRGRARAT SWY

Antigen sequence identity:

  • Mouse: 98%
  • Rat: 99%

Target Information

This gene encodes an abundant nuclear protein that binds with high affinity to nascent poly(A) tails. The protein 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 to about 250 nt.
At steady-state, this protein is localized in the nucleus, while a different poly(A) binding protein is localized in the cytoplasm.
Expansion of the GCG trinucleotide repeat from 6 to 8–13 copies in this gene leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD).
Related pseudogenes have been identified on chromosomes 19 and X. Read-through transcription also exists between this gene and the neighboring upstream BCL2-like 2 (BCL2L2) gene.


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

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