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Thermo Fisher Scientific PAM Polyclonal Antibody
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Thermo Fisher Scientific PAM Polyclonal Antibody

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Thermo Fisher Scientific의 PAM 폴리클로날 항체는 Western blot, IHC(P), ICC/IF에 적합합니다. Human PAM 단백질을 면역원으로 사용하였으며, 항원 친화 크로마토그래피로 정제되었습니다. 0.1 mg/mL 농도의 액상 형태로 제공되며, 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 02. 오후 01:35
Thermo Fisher Scientific PA559929 PAM Polyclonal Antibody 100 ul pk판매 단위 pk ·
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799,600원VAT 포함 879,560원

Thermo Fisher Scientific · Thermo Fisher Scientific PAM Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution Publications
Western Blot (WB) 0.04–0.4 µg/mL View 1 publication
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:500 -
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL -

Product Specifications

항목 내용
Species Reactivity Human
Published Species Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human PAM. Recombinant protein control fragment (Product # RP-88689)
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, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2645191

Product Specific Information

Immunogen sequence:
HLGKVVSGYR VRNGQWTLIG RQSPQLPQAF YPVGHPVDVS FGDLLAARCV FTGEGRTEAT HIGGTSSDEM CNLYIMYYME AKHAVSFMTC TQNVAPDMFR TIPPEANIPI PVKSDMVMMH EHHKETEYKD KIPLLQQPKR EEEEVL

Highest antigen sequence identity to the following orthologs:

  • Mouse: 90%
  • Rat: 88%

Target Information

SNX33 (sorting nexin-33), also known as SH3PX3, SH3PXD3C, or SNX30, is a 574 amino acid protein that interacts with ADAM15 and FAS-L.
Belonging to the sorting nexin family, SNX33 contains one BAR domain, one PX (phox homology) domain, and one SH3 domain.
The gene encoding SNX33 spans over 14,000 bases and maps to human chromosome 15q24.2.
Chromosome 15 comprises approximately 106 million base pairs and encodes more than 700 genes, representing about 3% of the human genome.
Angelman and Prader-Willi syndromes are associated with loss or deletion of genes in the 15q11–q13 region.


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

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