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SNRNP200 Recombinant antibody, PBS Only

SNRNP200 Uni-rAbTM Recombinant Antibody for WB, Indirect ELISA
Cat No. 84992-5-PBS
Clone No.242550D10

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, Indirect ELISA

HELIC2, EC:3.6.4.13, BRR2, ASCC3L1, Activating signal cointegrator 1 complex subunit 3-like 1

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

-/ -


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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

84992-5-PBS targets SNRNP200 in WB, Indirect ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen SNRNP200 fusion protein Ag20748 相同性解析による交差性が予測される生物種
Full Name small nuclear ribonucleoprotein 200kDa (U5)
Calculated molecular weight 494 aa, 57 kDa
Observed molecular weight200-245 kDa
GenBank accession numberBC001417
Gene Symbol SNRNP200
Gene ID (NCBI) 23020
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purification
UNIPROT IDO75643
Storage Buffer PBS only , pH 7.3
Storage ConditionsStore at -80°C.

Background Information

SNRNP200 (small nuclear ribonucleoprotein 200kDa (U5)), also known as HELIC2, ASCC3L1 or BRR2, is a 2,136 amino acid protein that localizes to the nucleus and contains two SEC63 domains, two helicase C-terminal domains and two helicase ATP-binding domains. Existing as multiple alternatively spliced isoforms, HELIC2 functions as an RNA helicase that is thought to promote specific RNA-RNA conformational changes which are important in the second step of RNA splicing. The gene encoding HELIC2 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8% of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the chromosome 2-localized ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes, hich also map to chromosome 2. The observed molecular weight of SNRNP200 is 200-245kd.

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