Skip to Content
Merck
All Photos(1)

Documents

MAB1900

Sigma-Aldrich

Anti-Integrin β1D Antibody, CT cytoplasmic domain, clone 2B1

clone 2B1, Chemicon®, from mouse

Synonym(s):

CD29

Sign Into View Organizational & Contract Pricing


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

2B1, monoclonal

species reactivity

canine, human, mouse

manufacturer/tradename

Chemicon®

technique(s)

immunocytochemistry: suitable
immunohistochemistry: suitable
western blot: suitable

isotype

IgG1

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... ITGB1(3688)

General description

Integrins are a family of heterodimeric membrane glycoproteins consisting of non-covalently associated alpha and beta subunits. More than 18 alpha and 8 beta subunits with numerous splice variant isoforms have been identified in mammals. In general, integrins function as receptors for extracellular matrix proteins. Certain integrins can also bind to soluble ligands or to counter-receptors on adjacent cells, such as the intracellular adhesion molecules (ICAMs), resulting in aggregation of cells. Signals transduced by integrins play a role in many biological processes, including cell growth, differentiation, migration and apoptosis. There are two major forms of integrin beta 1:beta 1A and beta 1D which differ in 13 amino acids. Their distribution pattern in adult tissues is mutually exclusive. Beta1A is present in all tissues, except cardiac and skeletal muscle, which instead express the beta1D variant.

Specificity

MAB1900 is specific for the cytoplasmic domain of integrin beta1D subunit. Integrin beta1D is present in cardiac and skeletal muscle. In proliferating C2C12 cells, beta1D is not expressed; C2C12 after differentiation into myotubes, however, express high levels of beta1D integrin. beta1D integrin was also found expressed in adult mouse extracts from heat, hind limb muscle, and tongue, with a faint band in skin. No reactivity was observed in extracts from lung, kidney, liver, or spleen {van der Flier et al, 1997}.

Immunogen

Epitope: C-terminus cytoplasmic domain
Synthetic peptide including an appending N-terminal cysteine: CQENPIYKSPINNFKNPNYGRKAGL coupled to KLH.

Application

Research Category
Cell Structure
Research Sub Category
Integrins
This Anti-Integrin β1D Antibody, C-terminus cytoplasmic domain, clone 2B1 is validated for use in WB, IC, IH for the detection of Integrin β1D.
Western Blotting: 1:100-1:1000; recognizes a 116kDa band in reduced, 7% PAGE-SDS westerns in differentiated C2C12 cells and some adult tissues {See van der Flier, 1997}. 1% SDS lysis buffer is recommended over RIPA or traditional reducing sample buffer.

Immunocytochemistry:

Immunohistochemistry: 1:25-1:200. Frozen, unfixed tissue sections, post-fixed with 2% PFA after primary and secondary antibody additions {van der Flier, 1997}. Alternatively, 4-7μm cyrosections fixed with cold acetone for 2 minutes and stored at -80°C until used. Airdried sections are rehydrated in PBS prior to use; detection via ABC systems is encouraged.

Optimal working dilutions must be determined by the end user.

Physical form

Format: Purified
Purified immunoglobulin. Liquid in PBS containing 0.09% sodium azide.

Storage and Stability

Maintain at 2-8°C in undiluted aliquots for up to 12 months from date of receipt.

Other Notes

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

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.

Not finding the right product?  

Try our Product Selector Tool.

Storage Class Code

12 - Non Combustible Liquids

WGK

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’.

Already Own This Product?

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

Visit the Document Library

Inhibition of collagen XVI expression reduces glioma cell invasiveness.
Bauer, R; Ratzinger, S; Wales, L; Bosserhoff, A; Senner, V; Grifka, J; Grassel, S
Cellular Physiology and Biochemistry null
Tanya A Baldwin et al.
The Journal of biological chemistry, 299(12), 105426-105426 (2023-11-06)
S-palmitoylation is a reversible lipid modification catalyzed by 23 S-acyltransferases with a conserved zinc finger aspartate-histidine-histidine-cysteine (zDHHC) domain that facilitates targeting of proteins to specific intracellular membranes. Here we performed a gain-of-function screen in the mouse and identified the Golgi-localized
Michelle S Parvatiyar et al.
JCI insight, 5 (2019-05-01)
In the current preclinical study, we demonstrate the therapeutic potential of sarcospan (SSPN) overexpression to alleviate cardiomyopathy associated with Duchenne muscular dystrophy (DMD) utilizing dystrophin-deficient mdx mice with utrophin haploinsufficiency that more accurately represent the severe disease course of human
Elizabeth M Gibbs et al.
Human molecular genetics, 30(3-4), 149-159 (2021-01-13)
The dystrophin-glycoprotein complex (DGC) is a membrane adhesion complex that provides structural stability at the sarcolemma by linking the myocyte's internal cytoskeleton and external extracellular matrix. In Duchenne muscular dystrophy (DMD), the absence of dystrophin leads to the loss of
Hafsa Mamsa et al.
Human molecular genetics, 31(5), 718-732 (2021-09-29)
In Duchenne muscular dystrophy (DMD), mutations in dystrophin result in a loss of the dystrophin-glycoprotein complex (DGC) at the myofiber membrane, which functions to connect the extracellular matrix with the intracellular actin cytoskeleton. The dystroglycan subcomplex interacts with dystrophin and

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