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Thermo Fisher Scientific Human Noggin Recombinant Protein, PeproTech
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Thermo Fisher Scientific Human Noggin Recombinant Protein, PeproTech

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인간 유래 Noggin 재조합 단백질로, HEK293 세포에서 발현된 고순도(≥95%) 단백질입니다. BMP 억제 활성을 가지며 다양한 세포 분화 및 발달 연구에 활용됩니다. 동결건조 형태로 제공되며, -20°C에서 보관합니다.

카탈로그번호
120-10C-01M
카테고리
Protein
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 05:56
Thermo Fisher Scientific 120-10C-01M Human Noggin Recombinant Protein, PeproTech 2 x 500 ug pk판매 단위 pk
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5,837,700원VAT 포함 6,421,470원

Thermo Fisher Scientific · Thermo Fisher Scientific Human Noggin Recombinant Protein, PeproTech

Applications

Immunohistochemistry (IHC)

Flow Cytometry (Flow)

Functional Assay (Functional)

Inhibition Assays (IA)

In vitro Assay (IV)

Miscellaneous PubMed (Misc)


Product Specifications

항목 내용
Species Human
Published Species Bovine, Chicken, Dog, Human, Mouse, Pig, Rat
Expression System HEK293 cells
Amino Acid Sequence QHYLHIRPAP SDNLPLVDLI EHPDPIFDPK EKDLNETLLR SLLGGHYDPG FMATSPPEDR PGGGGGAAGG AEDLAELDQL LRQRPSGAMP SEIKGLEFSE GLAQGKKQRL SKKLRRKLQM WLWSQTFCPV LYAWNDLGSR FWPRYVKVGS CFSKRSCSVP EGMVCKPSKS VHLTVLRWRC QRRGGQRCGW IPIQYPIISE CKCSC
Molecular Weight 46 kDa
Class Recombinant
Type Protein
Purity ≥ 95% by SDS-PAGE gel and HPLC analyses
Endotoxin Concentration <1 EU/µg
Activity Inhibits 5.0 ng/ml of BMP-4 induced alkaline phosphatase production by ATDC-5 chondrogenic cells. Expected ED50: 2.0–3.0 ng/ml
Conjugate Unconjugated
Form Lyophilized
Purification Purified
Contains No preservative
Storage Conditions -20°C

Product Specific Information

  • Catalog No. 120-10C-1MG is supplied as 2 × 500 µg (Cat. No. 120-10C-500UG).
  • Recombinant Human Noggin is a 46 kDa disulfide-linked homodimer consisting of two 205 amino acid chains.
  • Monomeric glycosylated Noggin migrates at approximately 28–33 kDa by SDS-PAGE under reducing conditions.
  • Shipped at ambient temperature. Refer to lot-specific Certificate of Analysis for storage, handling, and reconstitution details.

Target Information

Noggin participates in multiple developmental processes, including neural tube fusion and joint formation. It functions as a bone morphogenetic protein (BMP) inhibitor and plays a key role in organ morphogenesis via WNT3A-mediated β-catenin stabilization.
Mutations in the Noggin gene are associated with proximal symphalangism (SYM1) and multiple synostoses syndrome (SYNS1), conditions characterized by joint fusion abnormalities.


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

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