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ADH7 Antibody (C-Term)Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

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United States
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Ordering Information
Catalog # Size Availability Price  
AP9703b 0.1 mg 400 ul In Stock $ 255.00 Add to cart
AP9703b-ev20 20 ug 100 ul In Stock $ 95.00 Add to cart
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ADH7 Antibody (C-Term) - Product info

ApplicationWB, IHC, FC, IF
  • Applications Legend:
  • W=Western Blotting
  • IP=Immunoprecipitation
  • IHC-P=Immunohistochemistry (Paraffin)
  • IF-IC=Immunofluorescence (Immunocytochemistry)
  • F=Flow Cytometry
Primary AccessionP40394
ReactivityHuman
Concentration0.25 mg/ml
IsotypeRabbit Ig
Calculated MW41481 Da

ADH7 Antibody (C-Term) - Additional info

Gene ID 131
Other Names
ADH7; Alcohol dehydrogenase class 4 mu/sigma chain; Alcohol dehydrogenase class IV mu/sigma chain; Gastric alcohol dehydrogenase; Retinol dehydrogenase
Target/Specificity
This ADH7 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 325~354 amino acids from the C-terminal region of human ADH7 Antibody (C-Term).
Dilution
WB~~1:100~500
IHC~~1:50~100
FC~~1:10~50
IF~~1:10~50
Format
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
ADH7 Antibody (C-Term) is for research use only and not for use in diagnostic or therapeutic procedures.

ADH7 Antibody (C-Term) - Protein Information

Name ADH7
Function
Could function in retinol oxidation for the synthesis of retinoic acid, a hormone important for cellular differentiation Medium-chain (octanol) and aromatic (m-nitrobenzaldehyde) compounds are the best substrates. Ethanol is not a good substrate but at the high ethanol concentrations reached in the digestive tract, it plays a role in the ethanol oxidation and contributes to the first pass ethanol metabolism
Cellular Location
Cytoplasm.
Tissue Location
Preferentially expressed in stomach.

ADH7 Antibody (C-Term) - Related products

AP9703b: ADH7 Antibody (C-Term)

DC14734: Human ADH7 cDNA Clone

LY12277a: ADH7 Over-expression Lysate

BP9703b: ADH7 Antibody (C-Term) Blocking Peptide

ADH7 Antibody (C-Term) - Application data

  • ADH7 Antibody (C-Term) (Cat. #AP9703b) western blot analysis in Jurkat,CEM,NCI-H460,K562,MDA-MB435 cell line lysates (35ug/lane).This demonstrates the ADH7 antibody detected the ADH7 protein (arrow).

  • ADH7 Antibody (C-Term) (Cat. #AP9703b) IHC analysis in formalin fixed and paraffin embedded lung tissue followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of the ADH7 Antibody (C-Term) for immunohistochemistry. Clinical relevance has not been evaluated.

  • ADH7 Antibody (C-Term) (Cat. #AP9703b) flow cytometric analysis of K562 cells (right histogram) compared to a negative control cell (left histogram).FITC-conjugated goat-anti-rabbit secondary antibodies were used for the analysis.

  • Confocal immunofluorescent analysis of ADH7 Antibody (C-Term) (Cat. #AP9703b) with NCI-H460 cell followed by Alexa Fluor® 488-conjugated goat anti-rabbit lgG (green). DAPI was used to stain the cell nuclear (blue).

ADH7 Antibody (C-Term) - Research Areas

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BACKGROUND

This gene encodes class IV alcohol dehydrogenase 7 mu or sigma subunit, which is a member of the alcohol dehydrogenase family. Members of this family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. The enzyme encoded by this gene is inefficient in ethanol oxidation, but is the most active as a retinol dehydrogenase; thus it may participate in the synthesis of retinoic acid, a hormone important for cellular differentiation. The expression of this gene is much more abundant in stomach than liver, thus differing from the other known gene family members.

REFERENCES

Kedishvili, N.Y., et al. J. Biol. Chem. 270(8):3625-3630(1995) Cheung, B., et al. Alcohol. Clin. Exp. Res. 19(1):185-186(1995) Farres, J., et al. Eur. J. Biochem. 224(2):549-557(1994) Pares, X., et al. FEBS Lett. 303(1):69-72(1992)