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Thermo Fisher Scientific GLI3 Recombinant Rabbit Monoclonal Antibody (8B1E2)
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Thermo Fisher Scientific GLI3 Recombinant Rabbit Monoclonal Antibody (8B1E2)

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GLI3 단백질을 표적하는 재조합 토끼 단클론 항체로, Western blot, ICC/IF, ELISA에 적합합니다. HEK293 발현 시스템 기반으로 높은 특이성과 재현성을 제공합니다. 인체, 마우스, 랫트 반응성이 확인되었으며 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 04. 오후 02:56
Thermo Fisher Scientific MA542801 GLI3 Recombinant Rabbit Monoclonal Antibody (8B1E2) 100 ul pk판매 단위 pk ·
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714,600원VAT 포함 786,060원

Thermo Fisher Scientific · Thermo Fisher Scientific GLI3 Recombinant Rabbit Monoclonal Antibody (8B1E2)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1 µg/mL

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone 8B1E2
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 1301–1580 of human Gli3 (P10071)
Conjugate Unconjugated
Form Liquid
Concentration 2 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 0.05% BSA, 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2911942

Product Specific Information

Positive test controls include: HeLa.

Immunogen sequence:
PNESAGSMVN GMQNQDPVGQ GYLAHQLLGD SMQHPGAGRP GQQMLGQISA TSHINIYQGP ESCLPGAHGM GSQPSSLAVV RGYQPCASFG GSRRQAMPRD SLALQSGQLS DTSQTCRVNG IKMEMKGQPH PLCSNLQNYS GQFYDQTVGF SQQDTKAGSF SISDASCLLQ GTSAKNSELL SPGANQVTST VDSLDSHDLE GVQIDFDAII DDGDHSSLMS GALSPSIIQN LSHSSSRLTT PRASLPFPAL SMSTTNMAIG DMSSLLTSLA EESKFLAVMQ


Target Information

This gene encodes a protein belonging to the C2H2-type zinc finger subclass of the Gli family.
They function as DNA-binding transcription factors and mediate Sonic hedgehog (Shh) signaling.
The encoded protein localizes in the cytoplasm and activates patched Drosophila homolog (PTCH) gene expression.
It is also implicated in embryogenesis.
Mutations in this gene are associated with Greig cephalopolysyndactyly syndrome, Pallister-Hall syndrome, preaxial polydactyly type IV, and postaxial polydactyly types A1 and B.


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

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