88 Results for "

ALDH1

" in MedChemExpress (MCE) Product Catalog:
Products (88)

88 Results for "ALDH1" in MCE Product Catalog:

Cat. No.: HY-P82286
Synonyms: FDH; FTHFD; 10-fTHF; 10-FTHFDH

Host:  

Rabbit

Application:  

WB

Reactivity:  

Mouse, Rat

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Cat. No.: HY-P82286A
Synonyms: FDH; FTHFD; 10-fTHF; 10-FTHFDH

Host:  

Rabbit

Application:  

WB

Reactivity:  

Mouse, Rat

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Cat. No.: HY-P83869A
Synonyms: FDH; FTHFD; 10-fTHF; 10-FTHFDH

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P7476
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ALDH1A3; Aldehyde Dehydrogenase 1 Family, Member A3; Prev. ALDH6; Acetaldehyde Dehydrogenase 6; Retinaldehyde Dehydrogenase 3; ALDH1A6; RALDH3; RALDH-3; Aldehyde Dehydrogenase 6; RALDH3; Aldehyde Dehydrogenase 1 Family, Member A3, Isoform CRA_b; MCOP8; Al
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P81724
Synonyms: ALDH1A2; RALDH2; Retinal dehydrogenase 2; RALDH 2; RALDH2; Aldehyde dehydrogenase family 1 member A2; Retinaldehyde-specific dehydrogenase type 2; RALDH(II)

Host:  

Rabbit

Application:  

WB

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-P7475
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ALDH1A2; RALDH 2; Aldehyde Dehydrogenase 1 Family Member A2; Aldehyde Dehydrogenase 1 Family, Member A2; RALDH2; Aldehyde Dehydrogenase Family 1 Member A2; Retinaldehyde-Specific Dehydrogenase Type 2; Retinaldehyde Dehydrogenase 2; Retinal Dehydrogenase 2
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P700646
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: ALDH1A2; RALDH 2; Aldehyde Dehydrogenase 1 Family Member A2; Aldehyde Dehydrogenase 1 Family, Member A2; RALDH2; Aldehyde Dehydrogenase Family 1 Member A2; Retinaldehyde-Specific Dehydrogenase Type 2; Retinaldehyde Dehydrogenase 2; Retinal Dehydrogenase 2
Species:  
Human
Source:  
P. pastoris
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Cat. No.: HY-187170
CAS No.: 3038211-56-9
BM-51 is a selective inhibitor of CYP4Z1, with a human IC50 value of 91.7 nM. BM-51 binds to amino acid residues of CYP4Z1, thereby inhibiting its enzymatic activity. BM-51 downregulates the protein expression of stem cell markers (ALDH1A1, SOX2, OCT3/4 and KLF4) in cancer cells, inhibits cancer cell migration and invasion, and exhibits low toxicity to normal cells/tissues. BM-51 suppresses tumor initiation capacity and enhances the chemotherapeutic efficacy of Doxorubicin (HY-15142A). BM-51 can be used in breast cancer-related research [1].
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