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C2571

Anti-Human IgG (Fc specific)-Cy3 antibody produced in goat

affinity isolated antibody, buffered aqueous solution

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Gabaryty przesyłkiSKUDostępnośćCena netto
1 mL
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1000,00 zł

Informacje o tej pozycji

UNSPSC Code:
12352203
NACRES:
NA.46
MDL number:
Conjugate:
CY3 conjugate
Clone:
polyclonal
Application:
IHC (p)
Citations:
16

1000,00 zł


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biological source

goat

Quality Level

conjugate

CY3 conjugate

antibody form

affinity isolated antibody

antibody product type

secondary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

human

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:50

shipped in

wet ice

storage temp.

2-8°C

target post-translational modification

unmodified

Application

Anti-Human IgG (Fc specific)-Cy3 antibody produced in goat was used to screen sera on glycopeptide microarrays at a dilution of 1:1000. It was used at a working dilution of 1:100 for immunohistochemistry analysis of mouse footpad sections incubated with human polyclonal anti-Leishmania serum.

Biochem/physiol Actions

IgG antibody subtype is the most abundant of serum immunoglobulins of the immune system. It is secreted by B cells and is found in blood and extracellular fluids and provides protection from infections caused by bacteria, fungi and viruses. Maternal IgG is transferred to fetus through the placenta that is vital for immune defense of the neonate against infections. The coupling of Cy3 to Anti-Human IgG (Fc specific) antibody allows for the visualization of proteins by fluorescent microscopy.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 1% bovine serum albumin and 15 mM sodium azide

Legal Information

Cy is distributed under license from Amersham Biosciences Limited.

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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C2821C2181A3312
antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

antibody form

affinity isolated antibody

conjugate

CY3 conjugate

conjugate

CY3 conjugate

conjugate

CY3 conjugate

conjugate

alkaline phosphatase conjugate

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:50

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:300

technique(s)

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:100

technique(s)

direct ELISA: 1:30,000, immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:50, western blot: 1:30,000

species reactivity

human

species reactivity

goat

species reactivity

mouse

species reactivity

human

biological source

goat

biological source

rabbit

biological source

sheep

biological source

goat

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice

shipped in

wet ice


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Klasa składowania

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable



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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

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Jed Paul et al.
Journal of immunological methods, 432, 57-64 (2016-02-24)
Enzyme-linked immunosorbent assays (ELISAs) have traditionally been used to detect alloantibodies in patient plasma samples post hematopoietic cell transplantation (HCT); however, protein microarrays have the potential to be multiplexed, more sensitive, and higher throughput than ELISAs. Here, we describe the
Jeffrey S Burgdorf et al.
Molecular psychiatry, 28(3), 1101-1111 (2022-12-10)
We developed an IGFBP2-mimetic peptide fragment, JB2, and showed that it promotes basal synaptic structural and functional plasticity in cultured neurons and mice. We demonstrate that JB2 directly binds to dendrites and synapses, and its biological activity involves NMDA receptor
Anna Chuprin et al.
Genes & development, 27(21), 2356-2366 (2013-11-05)
Cellular senescence limits proliferation of potentially detrimental cells, preventing tumorigenesis and restricting tissue damage. However, the function of senescence in nonpathological conditions is unknown. We found that the human placental syncytiotrophoblast exhibited the phenotype and expressed molecular markers of cellular



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SKUNUMER GTIN
C2571-1ML04061833484227

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