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Thermo Fisher Scientific CGREF1 Polyclonal Antibody
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Thermo Fisher Scientific CGREF1 Polyclonal Antibody

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Human CGREF1 단백질에 특이적인 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot 및 IHC(P)에서 검증됨. 항원 친화 크로마토그래피로 정제된 액상 항체로, 장기 보관 시 -20°C에서 안정적. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 07. 28. 오전 12:44
Thermo Fisher Scientific PA552536 CGREF1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific CGREF1 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 0.04–0.4 µg/mL

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human CGREF1. Recombinant protein control fragment (Product #RP-89919).
Conjugate Unconjugated
Form Liquid
Concentration 0.2 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_2639737

Product Specific Information

Immunogen sequence:
PKDGVTRPDS EVQHQLLPNP FQPGQEQLGL LQSYLKGLGR TEVQLEHLSR EQVLLYLFAL HDYDQSGQLD GLELLSMLTA ALAPGAANSP TTNPVILIVD KVLETQDLNG DGLMTPAELI NFPGVALRHV EPG

Highest antigen sequence identity to the following orthologs:

  • Mouse: 75%
  • Rat: 72%

Target Information

CGREF1 (cell growth regulator with EF-hand domain 1), also known as CGR11, is a 301 amino acid secreted protein containing two highly conserved calcium-binding EF-hand domains required for mediating cell-cell adhesion. Induced by p53, CGREF1 inhibits cell growth in various cell lines.
CGREF1 is encoded by a gene located on human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome.
Harlequin ichthyosis (skin deformity) is associated with mutations in the ABCA12 gene, while sitosterolemia is linked to defects in ABCG5 and ABCG8 genes. Alstrom syndrome, a rare recessive disorder, is caused by mutations in the ALMS1 gene on chromosome 2.


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

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