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Thermo Fisher Scientific SHH Monoclonal Antibody (8G3)
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Thermo Fisher Scientific SHH Monoclonal Antibody (8G3)

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인간 SHH 단백질을 검출하는 Mouse IgG1 단클론 항체로, ELISA 및 Western blot에 적합합니다. 비결합형 액상 형태이며, 장기 보관 시 -20°C에서 보관 권장됩니다. 배아 발생 관련 SHH 연구에 활용됩니다.

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마지막 업데이트 2025. 08. 03. 오후 09:14
Thermo Fisher Scientific MA515647 SHH Monoclonal Antibody (8G3) 100 ul pk판매 단위 pk ·
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678,400원VAT 포함 746,240원

Thermo Fisher Scientific · Thermo Fisher Scientific SHH Monoclonal Antibody (8G3)

Thermo Fisher Scientific SHH Monoclonal Antibody (8G3)

Applications and Tested Dilutions

  • Western Blot (WB): 1:500–1:2,000
  • ELISA: 1:10,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 8G3
Immunogen Purified recombinant fragment of human SHH expressed in E. coli
Conjugate Unconjugated
Form Liquid
Concentration Not Determined
Storage Buffer Ascites
Contains 0.03% sodium azide
Storage Conditions Store at 4°C (short term). For long-term storage, store at -20°C. Avoid freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_10989461

Product Specific Information

MA5-15647 targets SHH in indirect ELISA and Western blot applications, showing reactivity with human samples.
The immunogen is a purified recombinant fragment of human SHH expressed in E. coli.
MA5-15647 detects SHH, which has a predicted molecular weight of approximately 49.6 kDa.

Target Information

Sonic Hedgehog (SHH) is expressed only during embryogenesis and plays a critical role in early embryo patterning. It is a key inductive signal in the development of the ventral neural tube, anterior-posterior limb axis, and ventral somites.
SHH is produced as a precursor that undergoes autocatalytic cleavage:

  • The N-terminal portion is soluble and responsible for signaling activity.
  • The C-terminal portion aids in precursor processing and attaches a cholesterol moiety to the N-terminal product, restricting it to the cell surface.

Defects in SHH or its signaling pathway cause holoprosencephaly (HPE), where the forebrain fails to separate properly, resulting in facial deformities.
Mutations may also be associated with VACTERL syndrome, characterized by vertebral, anal, tracheoesophageal, renal, cardiac, and limb anomalies.

Usage Note

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

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