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Thermo Fisher Scientific CYP17A1 Recombinant Rabbit Monoclonal Antibody (JB93-32)
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Thermo Fisher Scientific CYP17A1 Recombinant Rabbit Monoclonal Antibody (JB93-32)

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CYP17A1 단백질을 표적으로 하는 재조합 토끼 단클론 항체로, Western blot, IHC, ICC, Flow cytometry 등 다양한 분석에 적합. Human 시료 반응성, 높은 특이성과 재현성 제공. Protein A 정제, -20°C 보관.

카탈로그번호
MA534697
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 09:47
Thermo Fisher Scientific MA534697 CYP17A1 Recombinant Rabbit Monoclonal Antibody (JB93-32) 100 ul pk판매 단위 pk ·
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598,300원VAT 포함 658,130원

Thermo Fisher Scientific · Thermo Fisher Scientific CYP17A1 Recombinant Rabbit Monoclonal Antibody (JB93-32)

Thermo Fisher Scientific CYP17A1 Recombinant Rabbit Monoclonal Antibody (JB93-32)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:50–1:200
Flow Cytometry (Flow) 1:50–1:100

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone JB93-32
Immunogen Recombinant protein within Human Cytochrome P450 17A1 (aa 81–240)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer TBS, pH 7.4, with 40% glycerol, 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles, store in dark
Shipping Conditions Wet ice
RRID AB_2848605

Product Specific Information

Positive Control: HepG2, Hela, SH-SY-5Y, human breast tissue, human kidney tissue, mouse kidney tissue.

Target Information

This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyze many reactions involved in drug metabolism and synthesis of cholesterol, steroids, and other lipids.
This protein localizes to the endoplasmic reticulum and has both 17α-hydroxylase and 17,20-lyase activities. It is a key enzyme in the steroidogenic pathway that produces progestins, mineralocorticoids, glucocorticoids, androgens, and estrogens.
Mutations in this gene are associated with isolated steroid-17α-hydroxylase deficiency, 17α-hydroxylase/17,20-lyase deficiency, pseudohermaphroditism, and adrenal hyperplasia.

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

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