Phospho-NDRG1 (Thr346) (F5) rabbit mAb

Name: Phospho-NDRG1 (Thr346) (F5) rabbit mAb
SKU: 2106

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2106

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Select Your Size	Price
200 uL (0.5 mg/mL)(2106)	$475.00
20 uL (0.5 mg/mL)(2106S)	$175.00

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$175.00

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Note

20 μL is enough antibody for at least 20 Western blots.

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Product Overview

Description	N-Myc down-regulated gene 1 (NDRG1) has been reported to be a direct transcriptional target of p53. NDRG1 appears to play a necessary, but not sufficient, role in apoptosis, though its exact mechanism of action remains unknown. NDRG1 expression is elevated in non-small cell lung cancer cells, promoting cancer growth and reducing cytotoxicity to certain anti-cancer drugs. NDRG1 is also elevated in solid tumors and is recognized as a negative prognostic indicator in breast cancer. Elevated NDRG1 expression is correlated with disease recurrence and metastasis in breast cancer. NDRG1 is phosphorylated by Sgk1, which itself is activated by mTORC2. Phosphorylation of NDRG1 at Thr346 promotes cellular differentiation in adipocytes.

Product Details

More Information
Applications	Flow Cytometry, WB
Clone	NDRG1T346-F5
Format	Unconjugated
Validated Reactivity	Human, Mouse
Cross Reactivity	Predicted to work with mouse, rat and other homologues.
Detection	Anti-Rabbit IgG
Clonality	Monoclonal
Immunogen	A synthetic phospho-peptide corresponding to residues surrounding Thr346 of human phospho NDRG1
Formulation	1X PBS, 0.02% NaN3, 50% Glycerol, 0.1% BSA
Isotype	Rabbit IgGk
Preparation	Protein A+G
Recommended Usage	1µg/mL – 0.001µg/mL. It is recommended that the reagent be titrated for optimal performance for each application. See product image legends for additional information.
Storage	-20ºC
Pseudonyms	Differentiation-related gene 1 protein, N-myc downstream-regulated gene 1 protein, Nickel-specific induction protein Cap43, Reducing agents and tunicamycin-responsive protein, RTP, Rit42
Uniprot ID	Q92597
References	Stein S, Thomas EK, Herzog B, Westfall MD, Rocheleau JV, Jackson II RS, Wang M, and Liang P. (2004) Journal of Biological Chemistry. 279:48930-48940. Du A, Jiang Y, and Fan C. (2018) International Journal of Medical Sciences. 15:1502-1507. Cai K, El-Merahbi R, Loeffler M, Mayer AE, and Sumara G. (2017) Scientific Reports 7:7191. Sevinsky CJ, Khan F, Kokabee L, Darehshouri A, Maddipati KR, and Conklin DS. (2018) Breast Cancer Research. 20:55.

Images

Flow cytometric analysis of THP1 cells secondary antibody only negative control (blue) or untreated (red) or treated with IFNα + IL-4 + pervanadate (green) using Phospho-NDRG1 (Thr346) antibody NDRG1T346-F5 at 0.05 µg/mL. Cat. #2106.

Peptide blocking flow cytometric analysis of THP1 cells secondary antibody only negative control (light blue) or untreated (orange) using isotype control antibody #2141 or untreated (red) or with IFNα + IL-4 + pervanadate (green) or untreated and blocked with phospho-peptide (black) or treated and blocked with phospho peptide (gold) or untreated and blocked with non-phospho peptide (dark blue) or treated and blocked with non-phospho peptide (purple) using Phospho-NDRG1 (Thr346) antibody NDRG1T346-F5 at 0.05 µg/mL. Cat. #2106.

Western blot analysis of C2C12 cell extract untreated or treated with LY294002 using 0.05 ug/mL Phospho-NDRG1 (Thr346) antibody NDRG1T346-F5 Cat. #2106.

Western blot analysis of C2C12 cell extract untreated or treated with LY294002 using 0.05 µg/mL Phospho-NDRG1 (Thr346) antibody NDRG1T346-F5 Cat. #2106 or Company C antibody at 0.07 µg/mL (manufacturer’s recommended concentration) developed using the same exposure.

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