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Merck

G9264

Sigma-Aldrich

Monoclonal Anti-Growth Associated Protein-43 antibody produced in mouse

clone GAP-7B10, ascites fluid

Szinonimák:

Anti-GAP-43

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

MDL-szám:
UNSPSC kód:
12352203
NACRES:
NA.41
konjugátum:
unconjugated
application:
IHC
WB
klón:
GAP-7B10, monoclonal
faj reaktivitás:
hamster, human, feline, rat, chicken, snake, mouse
citations:
53
technika/technikák:
immunohistochemistry: suitable
western blot: 1:2,000 using newborn rat brain extract

biológiai forrás

mouse

Minőségi szint

konjugátum

unconjugated

antitest forma

ascites fluid

antitest terméktípus

primary antibodies

klón

GAP-7B10, monoclonal

molekulatömeg

antigen 46 kDa

tartalmaz

15 mM sodium azide

faj reaktivitás

hamster, human, feline, rat, chicken, snake, mouse

technika/technikák

immunohistochemistry: suitable
western blot: 1:2,000 using newborn rat brain extract

izotípus

IgG2a

UniProt elérési szám

kiszállítva

dry ice

tárolási hőmérséklet

−20°C

célzott transzláció utáni módosítás

unmodified

Géninformáció

human ... GAP43(2596)
mouse ... Gap43(14432)
rat ... Gap43(29423)

Általános leírás

Monoclonal Anti-Growth Associated Protein-43 (mouse IgG2a isotype) is derived from the GAP-7B10 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with HPLC-purified GAP-43 from neonatal rat forebrain membranes. Growth Associated Protein 43 (GAP-43) has a very acidic pI (4.3-4.6, depending on the species) and an anomalous behavior in SDS gels such that its reported molecular mass ranges from 43-57 kDa whereas, the primary sequence of the protein and its hydrodynamic behavior indicate a molecular mass of about 24 kDa.

Egyediség

Recognizes an epitope present on both kinase C phosphorylated and dephosphorylated forms of GAP-43.

Immunogén

GAP-43 from neonatal rat forebrain membranes.

Alkalmazás

Monoclonal Anti-Growth Associated Protein-43 antibody produced in mouse has been used in enzyme linked immunosorbent assay (ELISA).
Monoclonal Anti-Growth Associated Protein-43 antibody produced in mouse is suitable for:
  • immunostaining of tissue sections from the prefrontal cortex and hippocampus of rat pups to recognize an epitope present on kinase C domain in the N terminal of GAP-43 protein
  • immunohistochemistry at a working dilution of 1:3000 using sections from fetal and adult brains of mice
  • immunofluorescence at a working dilution of 1:4000 using 8μm sections of mice brain
  • western blotting using hippocampal lysates from rats
It is also suitable for immunoblotting at a working dilution of 1:2000 using newborn rat brain extract. The antibody is useful in the study of the role and function of GAP-43 during axonogenesis and in the adult nervous system.

Biokémiai/fiziológiai hatások

Growth Associated Protein 43(GAP-43) precise function in growth cones and synaptic terminals is not known, increased phosphorylation of GAP-43 correlates with exocytosis, depolarization, and treatment of growth cones with NGF, implying that kinase C and possibly other protein kinase-mediated phosphorylation of GAP-43 could be a component of a common response of growth cones to diverse extracellular stimuli. GAP43 associates with the plasma membrane via acylated residues near the amino terminus and with the submembrane fraction of the cytoskeleton, presumably through its highly charged, extended carboxyl terminus, which bears similarities to neurofilament proteins. Monoclonal antibody reacting specifically against GAP-43 is a useful tool in the study of the role and function of GAP-43 during axonogenesis and in the adult nervous system.
The neural-specific Growth-Associated Protein-43 (GAP-43) is an intracellular phosphoprotein found exclusively in the peripheral and central nervous systems. The axonal growth cones that are involved in the functions of motility and pathfinding during axonogenesis and regeneration contain GAP-43. Phosphorylation of GAP-43 is associated with exocytosis, depolarization and treatment of growth cones with nerve growth factor (NGF).

Jogi nyilatkozat

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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Tárolási osztály kódja

10 - Combustible liquids

WGK

WGK 2

Lobbanási pont (F)

Not applicable

Lobbanási pont (C)

Not applicable


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Analitikai tanúsítványok (COA)

Lot/Batch Number

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Az ügyfelek ezeket is megtekintették

Ming-Shu Xu et al.
Evidence-based complementary and alternative medicine : eCAM, 2013, 137631-137631 (2013-12-19)
Background. Cerebral ischemia is known to produce brain damage and related behavioural deficits, including memory deficits and motor disorders. Evidence shows that EA significantly promotes recovery of neurological function and thus improves quality of life. Objective. Evidence exists for the
K F Meiri et al.
Proceedings of the National Academy of Sciences of the United States of America, 83(10), 3537-3541 (1986-05-01)
Growth-associated protein, GAP-43, is a polypeptide that is induced in neurons when they grow axons. We show by means of subcellular fractionation and immunohistochemical localization that GAP-43 is a component of neuronal growth cones as well as growing neurites; it
Regulation of GAP-43 at serine 41 acts as a switch to modulate both intrinsic and extrinsic behaviors of growing neurons, via altered membrane distribution
Nguyen L, et al.
Molecular and Cellular Neurosciences, 41(1), 62-73 (2009)
Xiaodong Li et al.
Journal of neurochemistry, 129(1), 72-84 (2013-11-06)
Retinal ganglion cells transmit the visual signal from the retina to the brain. We have previously shown that the activator protein 2 (AP-2)δ (TFAP2D) transcription factor is expressed in one third of ganglion cells in developing retina suggesting a specialized
Axonal growth-associated proteins.
J H Skene
Annual review of neuroscience, 12, 127-156 (1989-01-01)

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