Skip to Content
Merck

MABE1017

Anti-OASIS/CREB3L1 Antibody, clone 44C7

clone 44C7, from mouse

Synonym(s):

Cyclic AMP-responsive element-binding protein 3-like protein 1, cAMP-responsive element-binding protein 3-like protein 1, Old astrocyte specifically-induced substance, OASIS, Processed cyclic AMP-responsive element-binding protein 3-like protein 1, OASIS

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

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

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Anti-OASIS/CREB3L1 Antibody, clone 44C7, clone 44C7, from mouse

biological source

mouse

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

44C7, monoclonal

species reactivity

mouse

technique(s)

western blot: suitable

isotype

IgG1κ

NCBI accession no.

NP_036087.2

UniProt accession no.

Q9Z125

shipped in

wet ice

target post-translational modification

unmodified

Quality Level

100

Gene Information

mouse ... Creb3L1(26427)

Analysis Note

Evaluated by Western Blotting in MC3T3-E1 mouse osteoblastic cell lysate.

Western Blotting Analysis: 2.0 µg/mL of this antibody detected OASIS/CREB3L1 in 10 µg of MC3T3-E1 mouse osteoblastic cell lysate.

Application

Research Category
Epigenetics & Nuclear Function
Research Sub Category
Nuclear Receptors
This Anti-OASIS/CREB3L1 Antibody, clone 44C7 is validated for use in Western Blotting for the detection of OASIS/CREB3L1.
Western Blotting Analysis: A representative lot detected full-length OASIS in lysates from untreated MC3T3-E1 murine osteoblastic cells and cleaved N-terminal OASIS fragment in lysates from MC3T3-E1 cells subjected to ER stresser thapsigargin or brefeldin A treatment (Murakami, T., et al. (2009). Nat. Cell Biol. 11(10):1205-1211).
Western Blotting Analysis: A representative lot detected a higher OASIS expression level in Hrd1-/- than in wild-type MEFs. A more elevated OASIS level was also detected in osteoblasts differentiated from Hrd1-/- than from wild-type MEFs following bone morphogenetic protein 2 (BMP2) treatment (Kondo, S., et al. (2012). Cell Death Differ. 19(12):1939-1949).

Biochem/physiol Actions

Expected to react with both spliced isoforms as well as the N-terminal fragment of cleaved Oasis.

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.

General description

Cyclic AMP-responsive element-binding protein 3-like protein 1 (UniProt Q9Z125; also known as BBF-2 homolog, cAMP-responsive element-binding protein 3-like protein 1, Old astrocyte specifically-induced substance) is encoded by the Creb3l1 (also known as Oasis) gene (Gene ID 26427) in murine species. Creb3l1 belongs to the the old astrocyte specifically induced substance (OASIS) family of transcription factors that function as ER stress transducers. OASIS members possess both a transcription-activation domain and a basic leucine zipper (bZIP) domain, as well as a transmembrane domain that allows them to associate with the ER. OASIS family members, except Luman (Creb3), exhibit cell- and tissue-specific expression patterns, with Oasis (Creb3l1) being preferentially expressed in osteoblasts and astrocytes, AIbZIP (Creb3l4, Creb4, Tisp40) in testis and prostate, Bbf2h7 (Creb3l2) in chondrocytes, and Crebh (Creb3l3) in hepatocytes. OASIS family members are activated in response to ER stress via a distinct mechanism than the ER unfold protein response (UPR) transducer ATF6. Oasis (Creb3l1) and Bbf2h7 (Creb3l2) are constantly ubiquitinated by the ER-resident E3 ubiquitin ligase HMG-CoA reductase degradation 1 (Hrd1) and degraded by proteasome under normal conditions. ER stress stabilizes Oasis and Bbf2h7 by inducing a dissociation of these transcription factors from Hrd1.
~62 and 52 kDa observed

Immunogen

Epitope: N-terminal half
Flag-tagged recombinant protein corresponding to the N-terminal half of mouse OASIS/CREB3L1.

Other Notes

Concentration: Please refer to lot specific datasheet.

Physical form

Format: Purified
Protein G Purified
Purified mouse monoclonal IgG1κ antibody in buffer containing 0.1 M Tris-Glycine (pH 7.4), 150 mM NaCl with 0.05% sodium azide.

Preparation Note

Stable for 1 year at 2-8°C from date of receipt.

Not finding the right product?  

Try our Product Selector Tool.

Storage Class

12 - Non Combustible Liquids

wgk

WGK 1

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Ayaha Yamamoto et al.
FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 35(2), e21158-e21158 (2020-11-06)
Prevention of kidney fibrosis is an essential requisite for effective therapy in preventing chronic kidney disease (CKD). Here, we identify Old astrocyte specifically induced substance (OASIS)/cAMP responsive element-binding protein 3-like 1 (CREB3l1), a CREB/ATF family transcription factor, as a candidate
Yoshiaki Miyake et al.
Communications biology, 5(1), 734-734 (2022-07-23)
Podocyte injury is involved in the onset and progression of various kidney diseases. We previously demonstrated that the transcription factor, old astrocyte specifically induced substance (OASIS) in myofibroblasts, contributes to kidney fibrosis, as a novel role of OASIS in the
Daisuke Ariyasu et al.
Endocrinology, 160(11), 2673-2691 (2019-08-23)
Isolated growth hormone deficiency type II (IGHD2) is mainly caused by heterozygous splice-site mutations in intron 3 of the GH1 gene. A dominant-negative effect of the mutant GH lacking exon 3 on wild-type GH secretion has been proposed; however, the

Related Content

New Products Flyer- Vol 4 Signaling Feature- NEW! Phosphohistidine Antibody

"Mods – modifications – small alterations can have a big impact on form and function. In the motorsports world, stock vehicles are modified to enhance their performance. Modifications, or mods, to the engine, drive train, intake and exhaust components add up to provide phenomenal performance gains that can be measured as horsepower and torque increases, which yield a competitive advantage, and result in reduced run times. In biology, proteins undergo modifications that alter their function. Some proteins require the modifications in order to perform their function effectively, whether it’s a pro-protein that is cleaved to produce an active enzyme, or a protein that is phosphorylated to facilitate a signaling process. Other proteins, such as histones, undergo modifications that regulate gene expression and alter cellular function. There are several post translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination that impact protein function and activity. As a result, the analysis of proteins and their post-translational modifications are particularly important for the study of normal and disease-associated processes. New antibodies to detect phospho Histidines are now available from EMD Millipore."

Post-Translational Modifications

Global Trade Item Number

SKUGTIN
MABE101704055977297447

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service