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

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Thermo Fisher Scientific의 ADAMTS2 Polyclonal Antibody는 인간 ADAMTS2 단백질을 인식하는 토끼 유래 다클론 항체입니다. IHC(P) 및 ICC/IF에 최적화되어 있으며, 항원 친화성 크로마토그래피로 정제되었습니다. 연구용으로만 사용 가능합니다.

카탈로그번호
PA555855
판매단위
pk
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마지막 업데이트 2025. 08. 03. 오전 06:55
Thermo Fisher Scientific PA555855 ADAMTS2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific ADAMTS2 Polyclonal Antibody

Applications and Tested Dilutions

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human ADAMTS2. Recombinant protein control fragment (Product #RP-93160)
Conjugate Unconjugated
Form Liquid
Concentration 0.3 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_2637665

Product Specific Information

Immunogen sequence:
VAMEVRPSPS TPLEVPLNAS STNATEDHPE TNAVDEPYKI HGLEDEVQPS NLIPRRPSPY EKTRNQRIQE LIDEMRKKEM LG

Sequence identity to orthologs:

  • Mouse: 72%
  • Rat: 71%

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, type II, and type 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 with no 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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