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Thermo Fisher Scientific RHEBL1 Polyclonal Antibody
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Thermo Fisher Scientific RHEBL1 Polyclonal Antibody

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Human RHEBL1 단백질을 인식하는 Rabbit Polyclonal 항체로, IHC(P) 검증 완료. 항원 친화 크로마토그래피로 정제되었으며, PBS 기반 버퍼에 보관. RhebL1 단백질의 세포 내 신호전달 및 NF-kappa-B 활성 연구에 적합.

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마지막 업데이트 2025. 08. 03. 오후 09:46
Thermo Fisher Scientific PA562732 RHEBL1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
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773,300원VAT 포함 850,630원

Thermo Fisher Scientific · Thermo Fisher Scientific RHEBL1 Polyclonal Antibody

Applications

  • Immunohistochemistry (Paraffin) (IHC (P)): 1:20–1:50

Product Specifications

항목 내용
Species Reactivity Human
Host/Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human RHEBL1. Recombinant protein control fragment (Product #RP-97807)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions Wet ice
RRID AB_2646533

Product Specific Information

Immunogen sequence:
MPLVRYRKVV ILGYRCVGKT SLAHQFVEGE FSEGYDPTVE NTYSKIVTLG KDEFHLHLV

Antigen sequence identity:

  • Mouse: 93%
  • Rat: 92%

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.

RhebL1 binds GTP and exhibits intrinsic GTPase activity. It may activate NF-kappa-B-mediated gene transcription and promote signal transduction through MTOR, activating RPS6KB1. It 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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