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Thermo Fisher Scientific CLC-7 (CLCN7) Polyclonal Antibody
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Thermo Fisher Scientific CLC-7 (CLCN7) Polyclonal Antibody

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Thermo Fisher Scientific의 CLC-7 (CLCN7) 폴리클로날 항체는 Mouse와 Rat 시료에서 반응하며, Western blot에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, PBS/BSA buffer에 보관됩니다. 연구용으로만 사용됩니다.

카탈로그번호
ACL-008-xxxxx (3개 옵션)
판매단위
pk
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카탈로그

3개 옵션
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마지막 업데이트 2025. 08. 04. 오전 05:01
Thermo Fisher Scientific ACL-008-200UL CLC-7 (CLCN7) Polyclonal Antibody 200 ul pk판매 단위 pk ·
재고 확인 필요
1,121,200원VAT 포함 1,233,320원
Thermo Fisher Scientific ACL-008-50UL CLC-7 (CLCN7) Polyclonal Antibody 50 ul pk판매 단위 pk ·
재고 확인 필요
923,800원VAT 포함 1,016,180원
Thermo Fisher Scientific ACL-008-25UL CLC-7 (CLCN7) Polyclonal Antibody 25 ul pk판매 단위 pk ·
재고 확인 필요
742,000원VAT 포함 816,200원

Thermo Fisher Scientific · Thermo Fisher Scientific CLC-7 (CLCN7) Polyclonal Antibody

Thermo Fisher Scientific CLC-7 (CLCN7) Polyclonal Antibody

Applications

  • Western Blot (WB)

Tested Dilution

  • 1:200

Product Specifications

항목 내용
Species Reactivity Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen (C)KDLARYRLGKGGLE, corresponding to amino acid residues 783–796 of rat CLC-7, intracellular, C-terminus
Conjugate Unconjugated
Form Lyophilized
Concentration 0.8 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.4, with 1% BSA
Contains 0.05% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Reconstitution: 25 µL, 50 µL, or 0.2 mL double distilled water (DDW), depending on sample size.
The antibody ships as a lyophilized powder at room temperature. Upon arrival, store at -20°C.
Reconstituted solution can be stored at 4°C for up to 1 week. For longer storage, aliquot and keep at -20°C.
Avoid multiple freeze/thaw cycles. Centrifuge all antibody preparations before use (10000 × g, 5 min).


Target Information

The CLCN7 gene encodes chloride channel 7, a member of the CLC chloride channel family.
Chloride channels function in plasma membranes and intracellular organelles.
Defects in this gene cause osteopetrosis types OPTB4 (autosomal recessive) and OPTA2 (autosomal dominant, Albers-Schonberg disease).
Osteopetrosis is a rare genetic disorder characterized by abnormally dense bone due to defective resorption of immature bone.
OPTA2 is the most common form, typically appearing in adolescence or adulthood.


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

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