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Merck
CN

SAB4200491

Anti-Adrenomedullin antibody produced in rabbit

~1.0 mg/mL, affinity isolated antibody

别名:

Anti-ADM, Anti-AM

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关于此项目

NACRES:
NA.41
UNSPSC Code:
51111800
Conjugate:
unconjugated
Clone:
polyclonal
Application:
ELISA (i), IHC
Citations:
2
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biological source

rabbit

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

species reactivity

human

concentration

~1.0 mg/mL

technique(s)

immunohistochemistry: 10-20 μg/mL using formalin-fixed paraffin-embedded human stomach, indirect ELISA: 50-100 ng/mL using human adrenomedullin

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... ADM(133)

General description

Adrenomedullin (ADM) is initially extracted from human pheochromocytoma. It is a member of the amylin/calcitonin gene-related peptide (CGRP) super-family. ADM is broadly distributed in many tissues during development and adulthood. It is most highly expressed in endothelial cells and vascular smooth muscle cells and is localized in highly vascularized tissues including the kidney, intestine, stomach, brain, lung, heart and placenta. The ADM gene is mapped to the human chromosome location 11p15.4.

Immunogen

synthetic peptide corresponding to a sequence at the C-terminus of human adrenomedullin (ADM), conjugated to KLH. The corresponding sequence is highly conserved in rat and mouse ADM (83% sequence identity).

Application

Anti-Adrenomedullin antibody produced in rabbit is suitable for use in immunohistochemistry and enzyme-linked immunosorbent assay (ELISA).

Biochem/physiol Actions

Adrenomedullin (ADM) exhibits a wide range of biological actions including vasorelaxant, diuretic, and cardiotonic effects. It blocks adipocyte differentiation and regulates glucose metabolism. ADM is a potent hypotensive and vasodilatory peptide. It modulates hormone release, natriuresis and antimicrobial effects. This circulating peptide also regulates the proliferation, migration and differentiation of various cell types. ADM plays a significant role in angiogenesis and pathological conditions including cardiovascular disease, ischemia and carcinogenesis. Productions of ADM are controlled by oxidative stress and inflammation-related substances like lipopolysaccharide and inflammatory cytokines. ADM and pro adrenomedullin N-terminal 20 peptide (PAMP) are derived from the same precursor pro adrenomedullin, by proteolytic processing. It exerts its effects via G-protein coupled calcitonin-like receptors (CRLR) complexed with either receptor activity-modifying protein-2 (RAMP2) or RAMP3.
Anti-Adrenomedullin specifically recognizes human ADM.

Physical form

Solution in 0.01 M phos­phate buffered saline, pH 7.4, containing 15 mM sodium azide.

Preparation Note

For continuous use, store at 2-8 °C for up to one month. For extended storage, freeze in working aliquots. Repeated freezing and thawing, or storage in “frost-free” freezers,is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilutions should be discarded if not used within 12 hours.

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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存储类别

10 - Combustible liquids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A genetic variant in the gene encoding adrenomedullin predicts the development of dysglycemia over 6.4 years in Chinese
Ong KL, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 412(3-4), 353-357 (2011)
Adrenomedullin and tumour microenvironment
Larrayoz IM, et al.
Journal of Translational Medicine, 12(1), 339-339 (2014)

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