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Thermo Fisher Scientific SHH Monoclonal Antibody (OTI10H6), TrueMAB
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Thermo Fisher Scientific SHH Monoclonal Antibody (OTI10H6), TrueMAB

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Sonic Hedgehog(SHH) 단백질을 인식하는 Mouse IgG1 단클론 항체로, WB 및 ICC/IF에 최적화됨. 인간, 개, 쥐 반응성. 동결건조 형태, PBS 버퍼 및 trehalose 포함. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 04. 오전 03:26
Thermo Fisher Scientific CF500041 SHH Monoclonal Antibody (OTI10H6), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific SHH Monoclonal Antibody (OTI10H6), TrueMAB

Applications

Western Blot (WB)

  • Tested Dilution: 1:1,000–1:2,000

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 1:100

Product Specifications

항목 내용
Species Reactivity Dog, Human, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI10H6
Immunogen Human recombinant protein fragment corresponding to amino acids 24–197 of human SHH 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 using this carrier-free antibody, perform an additional desalting step using Zeba Spin Desalting Columns (7K MWCO, 0.5 mL, Product #89882).


Target Information

Sonic Hedgehog (SHH) is expressed during embryogenesis and plays a crucial role in early embryo patterning. It acts as a key inductive signal for ventral neural tube formation, limb axis determination, and ventral somite development.
The SHH protein is synthesized as a precursor that undergoes autocatalytic cleavage. The N-terminal fragment is soluble and mediates signaling, while the C-terminal fragment aids in precursor processing. The C-terminal product attaches a cholesterol moiety to the N-terminal product, restricting its diffusion on the cell surface.
Defects in SHH or its signaling pathway can cause holoprosencephaly (HPE), characterized by forebrain malformation and facial deformities, and may be associated with VACTERL syndrome involving vertebral, anal, tracheoesophageal, renal, cardiac, and limb abnormalities.


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

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