27315-1-AP
antibody from Proteintech Group
Targeting: STAMBPL1
ALMalpha, AMSH-FP, AMSH-LP, bA399O19.2, FLJ31524, KIAA1373
Antibody data
- Antibody Data
- Antigen structure
- References [4]
- Comments [0]
- Validations [0]
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- Product number
- 27315-1-AP - Provider product page

- Provider
- Proteintech Group
- Product name
- STAMBPL1 antibody
- Antibody type
- Polyclonal
- Description
- STAMBPL1 antibody (Cat. #27315-1-AP) is a rabbit polyclonal antibody that shows reactivity with human and has been validated for the following applications: IHC, WB,ELISA.
- Reactivity
- Human
- Host
- Rabbit
- Conjugate
- Unconjugated
- Isotype
- IgG
- Vial size
- 20ul, 150ul
Submitted references A MYC-STAMBPL1-TOE1 positive feedback loop mediates EGFR stability in hepatocellular carcinoma.
STAMBPL1, transcriptionally regulated by SREBP1, promotes malignant behaviors of hepatocellular carcinoma cells via Wnt/β-catenin signaling pathway.
A multi-omic analysis reveals that Gamabufotalin exerts anti-hepatocellular carcinoma effects by regulating amino acid metabolism through targeting STAMBPL1.
STAMBPL1 promotes the progression of lung adenocarcinoma by inhibiting DHRS2 expression.
Zhang H, Wang Z, Zhang J, Li Z, Liu J, Yu J, Zhao Y, Guo F, Chen WD, Wang YD
Cell reports 2024 Oct 22;43(10):114812
Cell reports 2024 Oct 22;43(10):114812
STAMBPL1, transcriptionally regulated by SREBP1, promotes malignant behaviors of hepatocellular carcinoma cells via Wnt/β-catenin signaling pathway.
Jin J, Wang Y, Hu Y
Molecular carcinogenesis 2024 Nov;63(11):2158-2173
Molecular carcinogenesis 2024 Nov;63(11):2158-2173
A multi-omic analysis reveals that Gamabufotalin exerts anti-hepatocellular carcinoma effects by regulating amino acid metabolism through targeting STAMBPL1.
Zheng P, Xu D, Cai Y, Zhu L, Xiao Q, Peng W, Chen B
Phytomedicine : international journal of phytotherapy and phytopharmacology 2024 Dec;135:156094
Phytomedicine : international journal of phytotherapy and phytopharmacology 2024 Dec;135:156094
STAMBPL1 promotes the progression of lung adenocarcinoma by inhibiting DHRS2 expression.
Yang X, Ling L, Li C, Hu T, Zhou C, Chen J, Wang Y, Hu L
Translational oncology 2023 Sep;35:101728
Translational oncology 2023 Sep;35:101728
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