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Thermo Fisher Scientific GATM Monoclonal Antibody (OTI1C9), TrueMAB
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Thermo Fisher Scientific GATM Monoclonal Antibody (OTI1C9), TrueMAB

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GATM 단백질을 인식하는 Mouse monoclonal antibody (Clone OTI1C9)로, Western blot, IHC, ICC, Flow cytometry에 적합. 인간 시료 반응성. Lyophilized 형태로 제공되며 PBS buffer에 8% trehalose 포함. 연구용으로만 사용 가능.

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마지막 업데이트 2025. 08. 04. 오후 10:00
Thermo Fisher Scientific CF503147 GATM Monoclonal Antibody (OTI1C9), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific GATM Monoclonal Antibody (OTI1C9), TrueMAB

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:150
Immunocytochemistry (ICC/IF) 1:100
Flow Cytometry (Flow) 1:100

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone OTI1C9
Immunogen Full length human recombinant protein of human GATM produced in HEK293 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 distilled water to achieve 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

AGAT (glycine amidinotransferase, also known as GATM or transamidinase) is a 423-amino acid enzyme belonging to the amidinotransferase family.
Encoded on human chromosome 15q21.1, AGAT forms a homodimer that localizes to mitochondrial inner membranes, peripheral membranes, and cytoplasm.
It is expressed in various tissues including brain, heart, liver, lung, salivary gland, skeletal muscle, and kidney (high expression).
AGAT catalyzes the biosynthesis of guanidinoacetate, a precursor of creatine, essential for energy metabolism in muscle.
Defects in AGAT are linked to arginine:glycine amidinotransferase deficiency, an autosomal recessive disorder characterized by developmental delay, mental retardation, and reduced brain creatine levels.
AGAT may play roles in embryonic and CNS development and in heart failure response via local creatine synthesis.


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

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