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Thermo Fisher Scientific RHEBL1 Polyclonal Antibody, MaxPab
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Thermo Fisher Scientific RHEBL1 Polyclonal Antibody, MaxPab

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RHEBL1 단백질을 인식하는 Thermo Fisher Scientific의 폴리클로날 항체로, Western blot에 적합합니다. Rabbit에서 생산된 IgG 형태이며, PBS(pH 7.4) 용액에 보존되어 있습니다. Affinity chromatography로 정제되었으며, -20°C에서 보관합니다.

카탈로그번호
H00121268-D01P
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 07:02
Thermo Fisher Scientific H00121268-D01P RHEBL1 Polyclonal Antibody, MaxPab 100 ug pk판매 단위 pk ·
재고 확인 필요
582,600원VAT 포함 640,860원

Thermo Fisher Scientific · Thermo Fisher Scientific RHEBL1 Polyclonal Antibody, MaxPab

Applications

Western Blot (WB)

  • Tested Dilution: 1–5 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen RHEBL1 (NP_653194.1, 1 a.a. – approximately 183 a.a.) full-length human protein
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Protein sequence:
MPLVRYRKVV ILGYRCVGKT SLAHQFVEGE FSEGYDPTVE NTYSKIVTLG KDEFHLHLVD TAGQDEYSIL PYSFIIGVHG YVLVYSVTSL HSFQVIESLY QKLHEGHGKT RVPVVLVGNK ADLSPEREVQ AVEGKKLAES WGATFMESSA RENQLTQGIF TKVIQEIARV ENSYGQERRC HLM


Target Information

RhebL1 (ras homolog enriched in brain-like protein 1), also known as Rheb2 or GTPase RhebL1, is a 183 amino acid protein that belongs to the small GTPase superfamily and Rheb family.
Localizing to the cell membrane as well as the cytoplasm, RhebL1 is ubiquitously expressed and is increased two-fold in many tumor cell lines.
RhebL1 exhibits GTPase activity and may activate NF-kappa-B-mediated gene transcription. Regulating the activity of Rictor, RhebL1 also promotes signal transduction.
RhebL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 12q13.12 and mouse chromosome 15 F1.
Human chromosome 12 encodes over 1,100 genes and comprises approximately 4.5% of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and trisomy 12p, which causes facial developmental defects and seizure disorders.
Binds GTP and exhibits intrinsic GTPase activity. May activate NF-kappa-B-mediated gene transcription. Promotes signal transduction through MTOR, activates RPS6KB1, and is a downstream target of the small GTPase-activating proteins TSC1 and TSC2.


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

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