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Thermo Fisher Scientific ALX4 Polyclonal Antibody
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Thermo Fisher Scientific ALX4 Polyclonal Antibody

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Human ALX4 단백질을 인식하는 Rabbit Polyclonal Antibody로, Western blot에 최적화되어 있습니다. 합성 펩타이드 면역원 사용, 고순도 친화 크로마토그래피 정제, PBS/sucrose 버퍼 보존. 다양한 종에서 높은 상동성을 보이며 연구용으로 적합합니다.

판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 02:43
Thermo Fisher Scientific PA5113569 ALX4 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
680,400원VAT 포함 748,440원

Thermo Fisher Scientific · Thermo Fisher Scientific ALX4 Polyclonal Antibody

Thermo Fisher Scientific ALX4 Polyclonal Antibody

Applications

  • Western Blot (WB): 0.2–1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide directed towards the middle region of human ALX4
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with 2% sucrose
Contains 0.09% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2884084

Product Specific Information

  • Immunogen sequence:
    GQTHMGSLFG AASLSPGLNG YELNGEPDRK TSSIAALRMK AKEHSAAISW
  • For short term use, store at 2–8°C up to 1 week.
  • For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Predicted homology:
    Cow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 100%; Human: 100%; Mouse: 92%; Rabbit: 100%; Rat: 100%

Target Information

This gene encodes a paired-like homeodomain transcription factor expressed in the mesenchyme of developing bones, limbs, hair, teeth, and mammary tissue.
Mutations in this gene cause parietal foramina 2 (PFM2), an autosomal dominant disease characterized by deficient ossification of the parietal bones.
Mutations also cause a form of frontonasal dysplasia with alopecia and hypogonadism, suggesting a role in craniofacial development, mesenchymal-epithelial communication, and hair follicle development.
Deletion of a segment of chromosome 11 containing this gene, del(11)(p11p12), causes Potocki-Shaffer syndrome (PSS), characterized by craniofacial anomalies, mental retardation, multiple exostoses, and genital abnormalities in males.
In mouse, this gene uses dual translation initiation sites located 16 codons apart.

Usage Note

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

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