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

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Thermo Fisher Scientific의 PABPN1 Polyclonal Antibody는 인간 PABPN1 단백질(1–50번 잔기)을 인식하는 Rabbit IgG 항체입니다. WB, IHC, IP 등 다양한 응용에 적합하며, 액상 형태로 제공되고 4°C에서 보관합니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 02. 오후 10:06
Thermo Fisher Scientific A303523AM PABPN1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
477,300원VAT 포함 525,030원
Thermo Fisher Scientific A303523AT PABPN1 Polyclonal Antibody 10 ul pk판매 단위 pk ·
재고 확인 필요
194,600원VAT 포함 214,060원

Thermo Fisher Scientific · Thermo Fisher Scientific PABPN1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:2,000–1:10,000
Immunohistochemistry (IHC) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:500–1:2,000
Immunoprecipitation (IP) 2–10 µg/mg lysate

Product Specifications

Property Description
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 1 and 50 of human Poly(A) Binding Protein, Nuclear 1 (PABPN1)
Conjugate Unconjugated
Form Liquid
Concentration 0.20 mg/mL
Storage Conditions 4°C
Shipping Conditions Wet ice

Product Specific Information

  • Recommended shelf life: 1 year from date of receipt
  • Application Note: For IHC, epitope retrieval with citrate buffer (pH 6.0) is recommended for FFPE tissue sections.
  • Based on 100% sequence identity, this antibody is predicted to react with Bovine.

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 poly(A) tail size to about 250 nt. At steady state, the protein is localized in the nucleus, whereas a different poly(A) binding protein is localized in the cytoplasm.

The gene contains a GCG trinucleotide repeat at the 5′ end of the coding region; expansion from 6 to 8–13 copies leads to autosomal dominant oculopharyngeal muscular dystrophy (OPMD). Related pseudogenes exist on chromosomes 19 and X. Read-through transcription also occurs 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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