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Thermo Fisher Scientific OSGEPL1 Polyclonal Antibody
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Thermo Fisher Scientific OSGEPL1 Polyclonal Antibody

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OSGEPL1 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody로, WB, IHC, ELISA 등 다양한 응용에 적합합니다. Human, Mouse, Rat 반응성을 가지며, 고순도 Affinity chromatography로 정제된 액상 형태입니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오전 10:18
Thermo Fisher Scientific PA5117114 OSGEPL1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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655,000원VAT 포함 720,500원

Thermo Fisher Scientific · Thermo Fisher Scientific OSGEPL1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:100
ELISA 1 µg/mL

Product Specifications

Specification Description
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 1–270 of human OSGEPL1 (NP_0717482)
Conjugate Unconjugated
Form Liquid
Concentration 0.88 mg/mL
Purification Affinity chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2901744

Product Specific Information

Positive Samples: Mouse heart, Mouse kidney, Mouse liver, Mouse testis, Rat liver, Rat brain

Immunogen Sequence:
MLILTKTAGV FFKPSKRKVY EFLRSFNFHP GTLFLHKIVL GIETSCDDTA AAVVDETGNV LGEAIHSQTE VHLKTGGIVP PAAQQLHREN IQRIVQEALS ASGVSPSDLS AIATTIKPGL ALSLGVGLSF SLQLVGQLKK PFIPIHHMEA HALTIRLTNK VEFPFLVLLI SGGHCLLALV QGVSDFLLLG KSLDIAPGDM LDKVARRLSL IKHPECSTMS GGKAIEHLAK QGNRFHFDIK PPLHHAKNCD FSFTGLQHVT DKIIMKKEKE

Target Information

OSGEPL1 (also known as Qri7) is a 414 amino acid protein belonging to the KAE1/YgjD family and exists as three alternatively spliced isoforms. It is required for the formation of a threonylcarbamoyl group on adenosine in tRNAs with codons beginning with adenine.
The OSGEPL1 gene spans approximately 16,568 bases and maps to human chromosome 2q32.2. Chromosome 2, consisting of about 237 million bases, encodes over 1,400 genes and represents roughly 8% of the human genome. Several genetic diseases are linked to genes on chromosome 2, including Harlequin ichthyosis (ABCA12 mutation), sitosterolemia (ABCG5/ABCG8 mutations), and Alstrom syndrome (ALMS1 mutation).

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

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