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SAB1400003

Sigma-Aldrich

Anti-ADH1C antibody produced in mouse

IgG fraction of antiserum, buffered aqueous solution

Synonym(s):

Anti-ADH3

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About This Item

UNSPSC Code:
12352203
NACRES:
NA.41

Pricing and availability is not currently available.

biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

IgG fraction of antiserum

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

human

technique(s)

western blot: 1 μg/mL

UniProt accession no.

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This Item
SAB1401005SAB5700849SAB1408871
Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

biological source

mouse

biological source

rabbit

biological source

rabbit

biological source

mouse

conjugate

unconjugated

conjugate

unconjugated

conjugate

-

conjugate

unconjugated

antibody form

IgG fraction of antiserum

antibody form

purified immunoglobulin

antibody form

affinity isolated antibody

antibody form

purified immunoglobulin

clone

polyclonal

clone

polyclonal

clone

polyclonal

clone

polyclonal

technique(s)

western blot: 1 μg/mL

technique(s)

western blot: 1 μg/mL

technique(s)

immunohistochemistry: 1:50-1:200, western blot: 1:500-1:2000

technique(s)

western blot: 1 μg/mL

General description

This gene encodes class I alcohol dehydrogenase, gamma subunit, which is a member of the alcohol dehydrogenase family. Members of this enzyme family metabolize a wide variety of substrates, including ethanol, retinol, other aliphatic alcohols, hydroxysteroids, and lipid peroxidation products. Class I alcohol dehydrogenase, consisting of several homo- and heterodimers of alpha, beta, and gamma subunits, exhibits high activity for ethanol oxidation and plays a major role in ethanol catabolism. Three genes encoding alpha, beta and gamma subunits are tandemly organized in a genomic segment as a gene cluster. (provided by RefSeq)

Immunogen

ADH1C (NP_000660.1, 1 a.a. ~ 375 a.a) full-length human protein.

Sequence
MSTAGKVIKCKAAVLWELKKPFSIEEVEVAPPKAHEVRIKMVAAGICRSDEHVVSGNLVTPLPVILGHEAAGIVESVGEGVTTVKPGDKVIPLFTPQCGKCRICKNPESNYCLKNDLGNPRGTLQDGTRRFTCSGKPIHHFVGVSTFSQYTVVDENAVAKIDAASPLEKVCLIGCGFSTGYGSAVKVAKVTPGSTCAVFGLGGVGLSVVMGCKAAGAARIIAVDINKDKFAKAKELGATECINPQDYKKPIQEVLKEMTDGGVDFSFEVIGRLDTMMASLLCCHEACGTSVIVGVPPDSQNLSINPMLLLTGRTWKGAIFGGFKSKESVPKLVADFMAKKFSLDALITNILPFEKINEGFDLLRSGKSIRTVLTF

Features and Benefits

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Physical form

Solution in phosphate buffered saline, pH 7.4

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Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable


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Effect of periods of non-use on biofilter performance.
Martin, F. Jason, and Raymond C. Loehr.
Journal of the Air & Waste Management Association (1995), 46, 539-546 (1996)
Robert L. Grob, PhD, Eugene F. Barry, PhD
Modern Practice of Gas Chromatography, 471-472 (2004)
Elefteria Psillakis et al.
Journal of chromatography. A, 999(1-2), 145-153 (2003-07-30)
A simple and efficient liquid-phase microextraction (LPME) technique using a hollow-fibre membrane, in conjunction with gas chromatography-mass spectrometry has been developed for the extraction and analysis of six phthalate esters in water samples. Parameters such as extraction solvent, agitation of
Solid-phase microextraction (SPME) for rapid field sampling and analysis by gas chromatography-mass spectrometry (GC-MS).
Hook, Gary L., et al.
TrAC, Trends in Analytical Chemistry, 21, 534-543 (2002)
Elefteria Psillakis et al.
Chemosphere, 54(7), 849-857 (2003-11-26)
The sonochemical degradation of aqueous solutions containing low concentrations of six phthalate esters at an ultrasonic frequency of 80 kHz has been investigated. Ultrasonic treatment was found capable of removing the four higher molecular mass phthalates (di-n-butyl phthalate, butylbenzyl phthalate

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