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

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RHEBL1 단백질을 인식하는 Thermo Fisher Scientific의 토끼 폴리클로날 항체로, IHC(P)에서 검증됨. 항원 친화 크로마토그래피로 정제되었으며 PBS 기반 완충액에 보관. 인간 시료에 반응하며 연구용으로 적합.

카탈로그번호
PA563919
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 06:14
Thermo Fisher Scientific PA563919 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

Tested Applications and Dilutions

  • 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-101851)
Conjugate Unconjugated
Form Liquid
Concentration 0.05 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_2646534

Product Specific Information

Immunogen sequence:
SSARENQLTQ GIFTKVIQEI ARVENSYGQE RRCHLM

Highest antigen sequence identity:

  • Mouse: 81%
  • Rat: 81%

Target Information

RhebL1 (ras homolog enriched in brain-like protein 1), also known as Rheb2 or GTPase RhebL1, is a 183 amino acid protein belonging to the small GTPase superfamily and Rheb family.
It localizes to the cell membrane and cytoplasm, is ubiquitously expressed, and shows increased expression in many tumor cell lines.
RhebL1 exhibits GTPase activity, may activate NF-kappa-B-mediated gene transcription, and regulates Rictor activity to promote signal transduction.
It exists as two alternatively spliced isoforms and is encoded by a gene located on human chromosome 12q13.12 and mouse chromosome 15 F1.
Human chromosome 12 encodes over 1,100 genes and represents approximately 4.5% of the human genome, associated with various disorders such as hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome, and trisomy 12p.

Functional characteristics:

  • Binds GTP and exhibits intrinsic GTPase activity
  • Activates NF-kappa-B-mediated gene transcription
  • Promotes signal transduction through MTOR and activates RPS6KB1
  • Acts downstream of TSC1 and TSC2

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

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