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Thermo Fisher Scientific ADAMTS2 Polyclonal Antibody
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Thermo Fisher Scientific ADAMTS2 Polyclonal Antibody

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ADAMTS2 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal 항체. Western blot 및 ELISA에 사용 가능하며, 인간 및 랫드 시료에 반응. 고순도의 액상 형태로 공급되며, -20°C 보관 필요. 연구용으로만 사용.

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마지막 업데이트 2025. 08. 05. 오전 03:48
Thermo Fisher Scientific PA587766 ADAMTS2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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618,800원VAT 포함 680,680원

Thermo Fisher Scientific · Thermo Fisher Scientific ADAMTS2 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 1029–1213 of human ADAMTS2 (O95450)
Conjugate Unconjugated
Form Liquid
Concentration 2.88 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2804394

Product Specific Information

  • Positive Samples: A-375, U-87MG, THP-1, Rat thymus
  • Cellular Location: Extracellular matrix, extracellular space

Immunogen Sequence:
PRNISDPSKK SYVVQWLSRP DPDSPIRKIS SKGHCQGDKS IFCRMEVLSR YCSIPGYNKL CCKSCNLYNN LTNVEGRIEP PPGKHNDIDV FMPTLPVPTV AMEVRPSPST PLEVPLNASS TNATEDHPET NAVDEPYKIH GLEDEVQPPN LIPRRPSPYE KTRNQRIQEL IDEMRKKEML GKF

Target Information

This gene encodes a member of the ADAMTS (a disintegrin and metalloproteinase with thrombospondin motifs) protein family. Members of this family share several distinct protein modules, including a propeptide region, a metalloproteinase domain, a disintegrin-like domain, and a thrombospondin type 1 (TS) motif. Individual members differ in the number of C-terminal TS motifs, and some have unique C-terminal domains. The enzyme encoded by this gene excises the N-propeptide of type I, II, and V procollagens. Mutations in this gene cause Ehlers-Danlos syndrome type VIIC, a recessively inherited connective-tissue disorder. Alternative splicing results in two transcript variants; the short transcript encodes a protein lacking significant procollagen N-peptidase activity.


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

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