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Thermo Fisher Scientific CIB4 Polyclonal Antibody
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Thermo Fisher Scientific CIB4 Polyclonal Antibody

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Human CIB4 단백질에 특이적인 Rabbit Polyclonal Antibody로, IHC(P) 등 다양한 응용에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS 버퍼와 글리세롤 포함. 연구용으로만 사용 가능하며, 장기 보관 시 -20°C 권장.

카탈로그번호
PA557532
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 08:58
Thermo Fisher Scientific PA557532 CIB4 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific CIB4 Polyclonal Antibody

Applications

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:200–1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human CIB4. Recombinant protein control fragment (Product #RP-96159).
Conjugate Unconjugated
Form Liquid
Concentration 0.5 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_2639819

Product Specific Information

Immunogen sequence:
ACPSLKIEYA FRIYDFNENG FIDEEDLQRI ILRLLNSDDM SEDLLMDLTN HVLSESDLDN DNMLSFSEFE HAMAKSPDFM NSFRIHFWGC

Highest antigen sequence identity to the following orthologs:

  • Mouse: 90%
  • Rat: 92%

Target Information

CIB4 (calcium and integrin-binding family member 4) is a 185 amino acid protein that contains three EF-hand domains. CIB4 is closely related to CIB, which has one less EF-hand domain and is known to bind to Integrin alpha II beta in platelets, playing a role in signal transduction.
The gene encoding CIB4 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome.
Harlequin ichthyosis, a rare and severe skin deformity, is associated with mutations in the ABCA12 gene, while lipid metabolic disorders such as sitosterolemia are linked to defects in ABCG5 and ABCG8 genes. Additionally, Alstrom syndrome, a rare recessive genetic disorder, is caused by mutations in the ALMS1 gene located on chromosome 2.


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

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