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LRP4 Recombinant antibody, PBS Only

LRP4 Uni-rAbTM Recombinant Antibody for WB, Indirect ELISA
Cat No. 84973-1-PBS
Clone No.242157D11

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat

Applications

WB, Indirect ELISA

LRP-4, LRP10, LRP 4, Low-density lipoprotein receptor-related protein 4, KIAA0816

Formulation:  PBS Only
PBS and Azide
PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -


ご購入について

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国内在庫・納期について

約2万点のプロテインテック製品をコスモバイオ社物流センター(国内)に在庫しています。国内在庫の有無はコスモバイオ社ホームページの「品番検索」でカタログ番号を検索して確認できます。


保証・サポートについて

テクニカルサポートまたはご購入後1年間の交換/補填対応を承ります。詳細はこちらをご覧ください。


Tested Applications

Recommended dilution

ApplicationDilution
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Product Information

84973-1-PBS targets LRP4 in WB, Indirect ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen LRP4 fusion protein Ag19413 相同性解析による交差性が予測される生物種
Full Name low density lipoprotein receptor-related protein 4
Calculated molecular weight 1905 aa, 212 kDa
Observed molecular weight245 kDa
GenBank accession numberBC136667
Gene Symbol LRP4
Gene ID (NCBI) 4038
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purfication
UNIPROT IDO75096
Storage Buffer PBS only , pH 7.3
Storage ConditionsStore at -80°C.

Background Information

LRP4 (low-density lipoprotein receptor-related protein 4), also known as multiple epidermal growth factor-like domains 7 (MEGF7), is a type I single transmembrane protein of the low-density lipoprotein receptor (LDLR) family. LRP4 is composed of a large extracellular region containing multiple LDLa repeats, EGF-like domains and β-propeller domains, a transmembrane region and a cytoplasmic region containing an NPxY motif and a PDZ-interacting motif (PMID: 26071838). LRP4 binds agrin and recruits it to the MuSK signaling complex, which is critical for neuromuscular junction formation (PMID: 17119023; 18957220). LPR4 mutation or malfunction is implicated in disorders including congenital myasthenic syndrome, myasthenia gravis, and diseases of bone or kidney (26071838).

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