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Key Documents

MAB2011

Sigma-Aldrich

Anti-Mucin MUC5AC Antibody, clone CLH2

clone CLH2, Chemicon®, from mouse

Synonym(s):

Gastric Mucin

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

mouse

Quality Level

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

CLH2, monoclonal

species reactivity

human

manufacturer/tradename

Chemicon®

technique(s)

ELISA: suitable
immunocytochemistry: suitable
immunohistochemistry: suitable (paraffin)
immunoprecipitation (IP): suitable
western blot: suitable

isotype

IgG1

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... MUC5AC(4586)

General description

Mucin-5AC (UniProt: P98088; also known as MUC5-AC, Gastric mucin, Major airway glycoprotein 1, Mucin-5 subtype AC tracheobronchial, Tracheobronchial mucin 1. TBM) is encoded by the MUC5AC (also known as MUC5) gene (Gene ID: 4586) in human. MUC5-AC is a gel-forming glycoprotein of gastric and respiratory tract epithelia that protects the mucosa from infection and chemical damage by binding to inhaled microorganisms and particles that are subsequently removed by mucociliary system. It is synthesized with a signal peptide (aa 1-27), which is later cleaved off to produce the mature form (aa 28-5654). MUC5-AC undergoes C-O- and N-glycosylated. O-glycosylation occurs on the second and last threonine of the threonine/serine-rich tandem repeats TTPSPVPTTSTTSA. C-mannosylation in the cysteine-rich subdomains may be required for proper folding of these regions and for export from the endoplasmic reticulum during biosynthesis. At its N- and C-termini are larger and more complex domains that are rich in cysteine and are involved in formation of the mucin polymers. These domains include sequences, including the D1, D2, D”, and D3 domains at the N-terminus and the D4, C, and CK domains at the C-terminus. MUC5-AC is overexpressed in a number of carcinomas. (Ref.: Pothuraju, R., et al. (2020). Mol. Cancer, 19: Article 37; Perez-Vilar, J., et al. (2004). Glycobiology. 14(4); 325-337).

Specificity

Antibody MAB2011 is specific for the MUC5AC tandem repeat of human mucin. No cross reactivity with other peptides from MUC2, 3, 6, or 7.

Immunoreactivity of MAB2011 has been detected in the following normal human epithelial tissues: bronchus, endocervix, stomach, and gallbladder. The predominant staining pattern in normal tissues is perinuclear. Antibody reactivity has been observed in foveolar and mucopeptic neck cells of normal gastric mucosa. The expression of MUC5AC has been frequently observed in gastric carcinomas and may be used as a marker of gastric differentiation.

The CLH2 antibody shows a weak reactivity with a high molecular weight smear characteristic of mucin from native mucin extract from normal gastric mucosa and from gastric diffuse carcinoma .

The antibody was generated by immunizing mice with a synthetic tandem repeat peptide The antibody recognizes the sequence TTSTTSAP within the tandem repeat of MUC5AC (1). It further recognizes glycosylated as well as unglycosylated MUC5AC.

Immunogen

Directed against a synthetic peptide of the MUC5AC tandem repeat.

Application

Anti-Mucin MUC5AC Antibody, clone CLH2 detects level of Mucin MUC5AC & has been published & validated for use in ELISA, IP, WB, IC, IH(P).
Research Category
Apoptosis & Cancer
Research Sub Category
Tumor Markers
Western blot:Clone CLH2 shows a weak reactivity with a high molecular weight smear characteristic of mucin from a native mucin extract from normal gastric mucosa and from gastric diffuse carcinoma. Typical dilution is 1:100.

Immunocytochemistry

Immunohistochemistry. Effective on frozen and paraffin sections at 1:1000-1:2000 dilution.

ELISA

Immunoprecipitation

Optimal working dilutions must be determined by end user.

Physical form

Format: Purified
Purified immunoglobulin. Liquid at 1 mg/mL in 0.02M phosphate buffer, 0.25 M sodium chloride, 0.1% sodium azide, pH 7.6.

Storage and Stability

Maintain refrigerated at 2-8°C in undiluted aliquots for up to 12 months.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class

10 - Combustible liquids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Clinicopathologic and prognostic significance of the histologic activity of noncancerous liver tissue in hepatitis B virus-associated hepatocellular carcinoma.
Irene O L Ng, Ronnie T P Poon, Tony W H Shek, Sheung T Fan
American Journal of Clinical Pathology null
Intestinal metaplasia of human stomach displays distinct patterns of mucin (MUC1, MUC2, MUC5AC, and MUC6) expression.
C A Reis, L David, P Correa, F Carneiro, C de Bolos, E Garcia, U Mandel, H Clausen et al.
Cancer Research null
Mucin glycosylation is altered by pro-inflammatory signaling in pancreatic-cancer cells.
Wu, YM; Nowack, DD; Omenn, GS; Haab, BB
Journal of Proteome Research null
Immunohistochemical study of the expression of MUC6 mucin and co-expression of other secreted mucins (MUC5AC and MUC2) in human gastric carcinomas.
C A Reis, L David, F Carvalho, U Mandel, C de Bolos, E Mirgorodskaya, H Clausen, M Sobrinho-Sim?es
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society null
Ludivine Canivet et al.
Journal of applied toxicology : JAT, 41(2), 203-215 (2020-08-09)
Air pollution is a public health issue and the toxicity of ambient particulate matter (PM) is well-recognized. Although it does not mostly contribute to the total mass of PM, increasing evidence indicates that the ultrafine fraction has generally a greater

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