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Thermo Fisher Scientific BCKDK Monoclonal Antibody (OTI11C9), TrueMAB
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Thermo Fisher Scientific BCKDK Monoclonal Antibody (OTI11C9), TrueMAB

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BCKDK 단백질을 인식하는 Mouse monoclonal antibody (Clone OTI11C9). Western blot, IHC, ICC/IF에 사용 가능. Human 시료 반응성. Lyophilized 형태로 제공되며 재구성 후 약 1 mg/mL 농도로 사용. 연구용으로만 사용 가능.

카탈로그번호
CF500685
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오전 02:15
Thermo Fisher Scientific CF500685 BCKDK Monoclonal Antibody (OTI11C9), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific BCKDK Monoclonal Antibody (OTI11C9), TrueMAB

Applications and Tested Dilutions

Application Tested Dilution
Western Blot (WB) 1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50
Immunocytochemistry (ICC/IF) 1:100

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI11C9
Immunogen Full length human recombinant protein of human BCKDK produced in HEK293T cell
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 of distilled water to obtain 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

The branched-chain alpha-keto acid dehydrogenase complex (BCKD) catalyzes the irreversible second step in the catabolism of branched-chain amino acids (isoleucine, leucine, and valine).
This complex includes three catalytic components:

  • E1: branched-chain alpha-keto acid decarboxylase
  • E2: dihydrolipoyl transacylase
  • E3: dihydrolipoamide dehydrogenase

BCKD activity is regulated by two enzymes: a kinase (BCKDK) and a phosphorylase.
BCKDK contains one histidine kinase domain and is ubiquitously expressed.
Defects in this pathway cause Maple Syrup Urine Disease (MSUD), characterized by accumulation of branched-chain amino acids and their keto acids, leading to encephalopathy and neurodegeneration if untreated.


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

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