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MAB1622

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Anti-Spectrin alpha chain (nonerythroid) Antibody, clone AA6

clone AA6, Chemicon®, from mouse

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Synonym(s):
(ALPHA)II-SPECTRIN, Alpha-II spectrin, Fodrin alpha chain, Spectrin, non-erythroid alpha chain, non-erythrocytic spectrin alpha, spectrin, alpha, non-erythrocytic 1 (alpha-fodrin), Fodrin α
eCl@ss:
32160702
NACRES:
NA.41

biological source

mouse

Quality Level

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

AA6, monoclonal

species reactivity

pig, guinea pig, rabbit, mouse, chicken, rat, human

species reactivity (predicted by homology)

mammals

manufacturer/tradename

Chemicon®

technique(s)

ChIP: suitable
immunohistochemistry: suitable
immunoprecipitation (IP): suitable
western blot: suitable

isotype

IgG1

suitability

not suitable for immunohistochemistry (Paraffin)

NCBI accession no.

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... SPTAN1(6709)

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This Item
ABN2264HPA007927MABN1727
Anti-SNTF (cleaved spectrin) serum, from rabbit

ABN2264

Anti-SNTF (cleaved spectrin)

species reactivity

pig, guinea pig, rabbit, mouse, chicken, rat, human

species reactivity

human, mouse, porcine

species reactivity

human

species reactivity

human, rat

biological source

mouse

biological source

rabbit

biological source

rabbit

biological source

mouse

antibody form

purified immunoglobulin

antibody form

serum

antibody form

affinity isolated antibody

antibody form

purified immunoglobulin

clone

AA6, monoclonal

clone

polyclonal

clone

polyclonal

clone

N393/76, monoclonal

UniProt accession no.

Q13813

UniProt accession no.

Q13813

UniProt accession no.

Q13813

UniProt accession no.

Q9H254

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General description

Non-erythroid Spectrin, also known as Fodrin, plays a role in stabilizing membrane structures, maintaining cell shape and linking the cytoskeleton to plasma membranes or intracellular vesicles. As one of the primary targets cleaved by activated caspases during apoptosis, the full-length ~240 kDa protein can be cleaved to yield an N-terminal product of ~150 kDa, and C-terminal products of ~120 and ~35 kDa.

Specificity

Specific for the 240, 150, and 120 kDa forms of alpha-spectrin/alpha-fodrin molecule of all mammalian nonerythroid cells and chicken alpha-spectrin.
Wide-mammalian reactivity is expected.

Immunogen

Chicken red blood cell membranes purified by hypotonic lysis and mechanical enucleation.

Application

Immunohistochemistry (IFA):
A 1:200-1:400 dilution of a previous lot was used in immunohistochemistry.
Does not work on paraffin sections.

Optimal working dilutions must be determined by end user.

Chromatin Immunopreciptiation:
A previous lot of this antibody was used to immunoprecipitate Spectrin Alpha from chromatin-associated protein extracts derived from normal human, HeLa, FA-A, and transduced FA-A cells (McMahon, L.W., et al. (1999). J. Biological Chem. 274:32904-32908).
Anti-Spectrin alpha chain (nonerythroid) Antibody, clone AA6 is an antibody against Spectrin alpha chain (nonerythroid) for use in IH, IP, WB, ChIP.
Research Category
Cell Structure
Research Sub Category
Cytoskeleton

Quality

Evaluated by Western Blot on staurosporine-treated HeLa lysates.

Western Blot Analysis:
1:500 dilution of this antibody detected N-, C- terminal Spectrin alpha/Fodrin alpha on 10 μg of staurosporine treated HeLa lysates.

Target description

~240 kDa full length product, ~150 kDa N-terminal cleaved product and ~120 kDa C-terminal product may be seen in varing amounts in lysates, depending on condition. The smaller sizes represent break down products seen during apoptosis.

Physical form

Format: Purified
Protein A purified
Purified mouse monoclonal IgG1 in buffer containing PBS with 1% BSA and 0.09% sodium azide.

Storage and Stability

Stable for 12 months at 2-8°C from date of receipt.

Analysis Note

Control
HeLa cells treated with staurosporine

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.

Storage Class

12 - Non Combustible Liquids

wgk_germany

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable


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Further analysis of the lens phenotype in Lim2-deficient mice.
Shi, Y; De Maria, AB; Wang, H; Mathias, RT; FitzGerald, PG; Bassnett, S
Investigative Ophthalmology & Visual Science null
D A Schreihofer et al.
Neuroscience, 158(2), 602-609 (2008-11-04)
Diets high in soy are neuroprotective in experimental stroke. This protective effect is hypothesized to be mediated by phytoestrogens contained in soy, because some of these compounds have neuroprotective effects in in vitro models of cell death. We tested the
M Curcio et al.
Cell death & disease, 6, e1645-e1645 (2015-02-13)
The glial cell line-derived neurotrophic factor (GDNF) has an important role in neuronal survival through binding to the GFRα1 (GDNF family receptor alpha-1) receptor and activation of the receptor tyrosine kinase Ret. Transient brain ischemia alters the expression of the
Jennifer J Schlezinger et al.
Toxicological sciences : an official journal of the Society of Toxicology, 98(1), 125-136 (2007-04-03)
Apoptosis is a critical event in the deletion of B lymphocytes prior to their migration to the periphery. Synthetic peroxisome proliferator activated receptor gamma (PPARgamma) agonists, including the drug GW7845 and the environmental contaminant mono-(2-ethylhexyl) phthalate, as well as an
Allopregnanolone prevents dieldrin-induced NMDA receptor internalization and neurotoxicity by preserving GABA(A) receptor function.
Briz, V; Parkash, J; Sanchez-Redondo, S; Prevot, V; Su?ol, C
Endocrinology null

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