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Thermo Fisher Scientific GEMIN2 Monoclonal Antibody (OTI6G4), TrueMAB
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Thermo Fisher Scientific GEMIN2 Monoclonal Antibody (OTI6G4), TrueMAB

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GEMIN2 단백질을 인식하는 마우스 모노클로날 항체로, Western blot에 최적화되어 있습니다. 인간, 마우스, 랫트 반응성을 가지며, 동결건조 형태로 제공됩니다. 연구용으로만 사용되며, SMN 복합체 관련 단백질 분석에 적합합니다.

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pk
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마지막 업데이트 2025. 08. 04. 오후 04:54
Thermo Fisher Scientific CF808823 GEMIN2 Monoclonal Antibody (OTI6G4), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific GEMIN2 Monoclonal Antibody (OTI6G4), TrueMAB

Thermo Fisher Scientific GEMIN2 Monoclonal Antibody (OTI6G4), TrueMAB

Applications

  • Western Blot (WB): Tested dilution 1:2,000

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI6G4
Immunogen Full length human recombinant protein of human SIP1 produced in E. coli
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • For reconstitution, add 100 µL distilled water to achieve a final antibody concentration of approximately 1 mg/mL.
  • For conjugation experiments, perform an additional desalting step using Zeba Spin Desalting Columns (7K MWCO, 0.5 mL, Product #89882).

Target Information

SIP1 is one of the proteins found in the SMN complex, which consists of the survival of motor neuron (SMN) protein and several gemin proteins. The SMN complex is localized to a subnuclear compartment called gems (gemini of coiled bodies) and is required for assembly of spliceosomal snRNPs and pre-mRNA splicing. SIP1 interacts directly with SMN and is required for formation of the SMN complex.
A knockout mouse targeting the mouse homolog of this gene exhibited disrupted snRNP assembly and motor neuron degeneration. However, knockdown of SIP1 mRNA in motor neurons showed normal motor axons, while knockdown of SMN mRNA caused abnormal motor axon outgrowth, indicating that SIP1 may have additional roles outside the SMN complex.

Usage Note

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

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