抗Human IGF-II R Fluorescein抗体(Anti-Human IGF-II R Fluorescein antibody)

掲載日情報:2018/11/26 現在Webページ番号:34128

Human IGF-II R Fluoresceinに対する抗体(Anti-Human IGF-II R Fluorescein )です。
本製品は研究用です。研究用以外には使用できません。

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Anti-Human IGF-II R Fluorescein Affinity Purified Polyclonal Ab (100 TESTS)
10日程度 ※ 表示されている納期は弊社に在庫がなく、取り寄せた場合の目安納期となります。 2
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説明文
別名:300 kDa mannose 6-phosphate receptor
Genbank No: 3482
Protein Accession No: P11717
法規制等
保存条件 4℃,暗所保存,凍結禁止 法規備考
抗原種 Human 免疫動物 Goat クラス IgG 標識 FITC
交差性 Human 適用 FCM
クロナリティ Polyclonal フォーマット 性状 Antigen Affinity Purified 吸収処理
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[在庫・価格 :2024年05月29日 00時00分現在]

※ 表示されている納期は弊社に在庫が無く、取り寄せた場合の納期目安となります。

Anti-Human IGF-II R Fluorescein Affinity Purified Polyclonal Ab (100 TESTS)

文献数: 2

説明文 別名:300 kDa mannose 6-phosphate receptor
Genbank No: 3482
Protein Accession No: P11717
法規制等
保存条件 4℃,暗所保存,凍結禁止 法規備考
抗原種 Human 免疫動物 Goat
交差性 Human 適用 FCM
標識 FITC 性状 Antigen Affinity Purified
吸収処理 クラス IgG
クロナリティ Polyclonal フォーマット
掲載カタログ

製品記事
関連記事



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Product Details

Species ReactivityHuman
LabelFluorescein
ImmunogenMouse myeloma cell line NS0-derived recombinant human IGF-II RSer1510-Phe2108Accession # P11717
SourcePolyclonal Goat IgG
PurificationAntigen Affinity-purified
SpecificityDetects human IGF-II R in direct ELISAs and Western blots.


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Applications and Data

 Recommended
Concentration
Sample
Flow Cytometry10 µL/106 cellsSee below


Flow Cytometry
Detection of IGF‑II R in Human Blood Monocytes by Flow Cytometry.
Human peripheral blood monocytes were stained with Goat Anti-Human IGF‑II R Fluorescein‑conjugated Antigen Affinity-purified Polyclonal Antibody (Catalog # FAB2447F, filled histogram) or isotype control antibody (Catalog # IC108F, open histogram). View our protocol for Staining Membrane-associated Proteins.


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Related Product & Information

BackgroundIGF-II R
background_contentBackground:
IGF-II R
The type 2 Insulin-like Growth Factor Receptor (IGF-II R; also known as cation-independent mannose-6 phosphate receptor/CI-MPR) is a 300 kDa member of the P-type lectin family of molecules. P-type lectins generate functional eukaryotic lysosomes by binding and sorting lysosomal enzymes expressing phosphorylated mannose residues (M6P) (1-3). IGF-II R is a type I transmembrane glycoprotein that contains a 2,264 amino acid (aa) extracellular region, a 23 aa transmembrane segment and a 124 aa cytoplasmic tail (4, 5). The extracellular region consists of 15 contiguous “binding” repeats of about 150 aa each. The odd-numbered repeats interact with “ligands” while the even-numbered repeats likely generate a nondisulfide homodimer in the membrane (1). Repeat #11 binds IGF‑II, while repeats 3 and 9 bind mannose-6 phosphate; repeat #13 contains a fibronectin type II motif and assists in IGF-II binding (1, 2). In the extracellular region of IGF‑II R expressed by R&D Systems (600 amino acids), human IGF-II R is 85% identical to both mouse and bovine IGF-II R. This expressed region includes binding repeats #11, 12, and 13. In addition to IGF-II, CI-MPR/IGF-II R binds non-M6P containing ligands such as retinoic acid, urokinase-type plasminogen-activator receptor and plasminogen, plus M6P-containing molecules such as lysosomal enzymes, TGF-beta 1 precursor, proliferin, LIF, CD26, herpes simplex glycoprotein D, and granzymes A and B (2, 6). IGF-II R regulates many diverse biological functions that range from intracellular trafficking to the internalization of extracellular factors and modulation of cellular responses. It delivers newly synthesized M6P-tagged lysosomal enzymes from the trans-golgi network to endosomes, and facilitates the clearance of extracellular lysosomal and matrix degrading enzymes by internalization into clathrin-coated vesicles and delivery into endosomes. With respect to IGF-II biology, it would appear that IGF-II R is principally a regulator of local IGF-II levels, targeting IGF-II for destruction in lysosomes (2). However, some evidence suggests the receptor will signal via G-proteins, an effect that has yet to be conclusively shown (6).


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Citations

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.
  1. Enhanced suppression of polyclonal CD8+25+ regulatory T cells via exosomal arming of antigen-specific peptide/MHC complexes
    Authors: C Mu, X Zhang, L Wang, A Xu, KA Ahmed, X Pang, R Chibbar, A Freywald, J Huang, Y Zhu, J Xiang
    J. Leukoc. Biol, 2017;0(0):.
    Species: Mouse
    Sample Type: Whole Cells
    Application: Flow

  2. Co-targeting the IGF system and HIF-1 inhibits migration and invasion by (triple-negative) breast cancer cells.
    Authors: Mancini M, Gariboldi M, Taiana E, Bonzi M, Craparotta I, Pagin M, Monti E
    Br J Cancer, 2014;110(12):2865-73.
    Species: Human
    Sample Type: Whole Cells
    Application: Flow



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