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Thermo Fisher Scientific SNRPN Polyclonal Antibody
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Thermo Fisher Scientific SNRPN Polyclonal Antibody

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SNRPN 단백질을 인식하는 토끼 폴리클로날 항체로, Western blot에 적합합니다. 인간 시료 반응성이 있으며, 합성 펩타이드 항원을 이용해 제작되었습니다. 액상 형태로 제공되며, -20°C에서 보관합니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오전 05:34
Thermo Fisher Scientific PA541767 SNRPN Polyclonal Antibody 100 ul pk판매 단위 pk ·
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630,500원VAT 포함 693,550원

Thermo Fisher Scientific · Thermo Fisher Scientific SNRPN Polyclonal Antibody

Applications

  • Western Blot (WB): 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide directed towards the N-terminal of human SNRPN (aa 46–95)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS with 2% sucrose
Contains 0.09% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2608337

Product Specific Information

Peptide sequence:
DEFRKIKPKN AKQPEREEKR VLGLVLLRGE NLVSMTVEGP PPKDTGIARV

Sequence homology:
Cow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 100%; Rabbit: 100%; Rat: 100%; Zebrafish: 93%

Target Information

The protein encoded by this gene is one polypeptide of a small nuclear ribonucleoprotein complex and belongs to the snRNP SMB/SMN family. The protein plays a role in pre-mRNA processing, possibly in tissue-specific alternative splicing events. Although individual snRNPs are believed to recognize specific nucleic acid sequences through RNA-RNA base pairing, the specific role of this family member is unknown. The protein arises from a bicistronic transcript that also encodes a protein identified as the SNRPN upstream reading frame (SNURF). Multiple transcription initiation sites have been identified and extensive alternative splicing occurs in the 5′ untranslated region. Additional splice variants have been described but sequences for the complete transcripts have not been determined. The 5′ UTR of this gene has been identified as an imprinting center. Alternative splicing or deletion caused by a translocation event in this paternally-expressed region is responsible for Angelman syndrome or Prader-Willi syndrome due to parental imprint switch failure.


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

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