BIRC6 Antibody - #DF13472
製品: | BIRC6 Antibody |
カタログ: | DF13472 |
タンパク質の説明: | Rabbit polyclonal antibody to BIRC6 |
アプリケーション: | WB IHC |
反応性: | Human, Mouse |
予測: | Pig, Zebrafish, Bovine, Sheep, Rabbit, Chicken, Xenopus |
分子量: | 530kDa; 530kD(Calculated). |
ユニプロット: | Q9NR09 |
RRID: | AB_2846491 |
製品説明
*The optimal dilutions should be determined by the end user.
*Tips:
WB: For western blot detection of denatured protein samples. IHC: For immunohistochemical detection of paraffin sections (IHC-p) or frozen sections (IHC-f) of tissue samples. IF/ICC: For immunofluorescence detection of cell samples. ELISA(peptide): For ELISA detection of antigenic peptide.
引用形式: Affinity Biosciences Cat# DF13472, RRID:AB_2846491.
折りたたみ/展開
Apollon; Apollon protein; Baculoviral IAP repeat containing 6; Baculoviral IAP repeat containing protein 6; Baculoviral IAP repeat-containing protein 6; BIR repeat containing ubiquitin conjugating enzyme; BIRC 6; BIRC6; BIRC6_HUMAN; BRUCE; FLJ13726; FLJ13786; KIAA1289; Ubiquitin conjugating BIR domain enzyme apollon; Ubiquitin-conjugating BIR domain enzyme apollon;
免疫原
- Q9NR09 BIRC6_HUMAN:
- Protein BLAST With
- NCBI/
- ExPASy/
- Uniprot
MVTGGGAAPPGTVTEPLPSVIVLSAGRKMAAAAAAASGPGCSSAAGAGAAGVSEWLVLRDGCMHCDADGLHSLSYHPALNAILAVTSRGTIKVIDGTSGATLQASALSAKPGGQVKCQYISAVDKVIFVDDYAVGCRKDLNGILLLDTALQTPVSKQDDVVQLELPVTEAQQLLSACLEKVDISSTEGYDLFITQLKDGLKNTSHETAANHKVAKWATVTFHLPHHVLKSIASAIVNELKKINQNVAALPVASSVMDRLSYLLPSARPELGVGPGRSVDRSLMYSEANRRETFTSWPHVGYRWAQPDPMAQAGFYHQPASSGDDRAMCFTCSVCLVCWEPTDEPWSEHERHSPNCPFVKGEHTQNVPLSVTLATSPAQFPCTDGTDRISCFGSGSCPHFLAAATKRGKICIWDVSKLMKVHLKFEINAYDPAIVQQLILSGDPSSGVDSRRPTLAWLEDSSSCSDIPKLEGDSDDLLEDSDSEEHSRSDSVTGHTSQKEAMEVSLDITALSILQQPEKLQWEIVANVLEDTVKDLEELGANPCLTNSKSEKTKEKHQEQHNIPFPCLLAGGLLTYKSPATSPISSNSHRSLDGLSRTQGESISEQGSTDNESCTNSELNSPLVRRTLPVLLLYSIKESDEKAGKIFSQMNNIMSKSLHDDGFTVPQIIEMELDSQEQLLLQDPPVTYIQQFADAAANLTSPDSEKWNSVFPKPGTLVQCLRLPKFAEEENLCIDSITPCADGIHLLVGLRTCPVESLSAINQVEALNNLNKLNSALCNRRKGELESNLAVVNGANISVIQHESPADVQTPLIIQPEQRNVSGGYLVLYKMNYATRIVTLEEEPIKIQHIKDPQDTITSLILLPPDILDNREDDCEEPIEDMQLTSKNGFEREKTSDISTLGHLVITTQGGYVKILDLSNFEILAKVEPPKKEGTEEQDTFVSVIYCSGTDRLCACTKGGELHFLQIGGTCDDIDEADILVDGSLSKGIEPSSEGSKPLSNPSSPGISGVDLLVDQPFTLEILTSLVELTRFETLTPRFSATVPPCWVEVQQEQQQRRHPQHLHQQHHGDAAQHTRTWKLQTDSNSWDEHVFELVLPKACMVGHVDFKFVLNSNITNIPQIQVTLLKNKAPGLGKVNALNIEVEQNGKPSLVDLNEEMQHMDVEESQCLRLCPFLEDHKEDILCGPVWLASGLDLSGHAGMLTLTSPKLVKGMAGGKYRSFLIHVKAVNERGTEEICNGGMRPVVRLPSLKHQSNKGYSLASLLAKVAAGKEKSSNVKNENTSGTRKSENLRGCDLLQEVSVTIRRFKKTSISKERVQRCAMLQFSEFHEKLVNTLCRKTDDGQITEHAQSLVLDTLCWLAGVHSNGPGSSKEGNENLLSKTRKFLSDIVRVCFFEAGRSIAHKCARFLALCISNGKCDPCQPAFGPVLLKALLDNMSFLPAATTGGSVYWYFVLLNYVKDEDLAGCSTACASLLTAVSRQLQDRLTPMEALLQTRYGLYSSPFDPVLFDLEMSGSSCKNVYNSSIGVQSDEIDLSDVLSGNGKVSSCTAAEGSFTSLTGLLEVEPLHFTCVSTSDGTRIERDDAMSSFGVTPAVGGLSSGTVGEASTALSSAAQVALQSLSHAMASAEQQLQVLQEKQQQLLKLQQQKAKLEAKLHQTTAAAAAAASAVGPVHNSVPSNPVAAPGFFIHPSDVIPPTPKTTPLFMTPPLTPPNEAVSVVINAELAQLFPGSVIDPPAVNLAAHNKNSNKSRMNPLGSGLALAISHASHFLQPPPHQSIIIERMHSGARRFVTLDFGRPILLTDVLIPTCGDLASLSIDIWTLGEEVDGRRLVVATDISTHSLILHDLIPPPVCRFMKITVIGRYGSTNARAKIPLGFYYGHTYILPWESELKLMHDPLKGEGESANQPEIDQHLAMMVALQEDIQCRYNLACHRLETLLQSIDLPPLNSANNAQYFLRKPDKAVEEDSRVFSAYQDCIQLQLQLNLAHNAVQRLKVALGASRKMLSETSNPEDLIQTSSTEQLRTIIRYLLDTLLSLLHASNGHSVPAVLQSTFHAQACEELFKHLCISGTPKIRLHTGLLLVQLCGGERWWGQFLSNVLQELYNSEQLLIFPQDRVFMLLSCIGQRSLSNSGVLESLLNLLDNLLSPLQPQLPMHRRTEGVLDIPMISWVVMLVSRLLDYVATVEDEAAAAKKPLNGNQWSFINNNLHTQSLNRSSKGSSSLDRLYSRKIRKQLVHHKQQLNLLKAKQKALVEQMEKEKIQSNKGSSYKLLVEQAKLKQATSKHFKDLIRLRRTAEWSRSNLDTEVTTAKESPEIEPLPFTLAHERCISVVQKLVLFLLSMDFTCHADLLLFVCKVLARIANATRPTIHLCEIVNEPQLERLLLLLVGTDFNRGDISWGGAWAQYSLTCMLQDILAGELLAPVAAEAMEEGTVGDDVGATAGDSDDSLQQSSVQLLETIDEPLTHDITGAPPLSSLEKDKEIDLELLQDLMEVDIDPLDIDLEKDPLAAKVFKPISSTWYDYWGADYGTYNYNPYIGGLGIPVAKPPANTEKNGSQTVSVSVSQALDARLEVGLEQQAELMLKMMSTLEADSILQALTNTSPTLSQSPTGTDDSLLGGLQAANQTSQLIIQLSSVPMLNVCFNKLFSMLQVHHVQLESLLQLWLTLSLNSSSTGNKENGADIFLYNANRIPVISLNQASITSFLTVLAWYPNTLLRTWCLVLHSLTLMTNMQLNSGSSSAIGTQESTAHLLVSDPNLIHVLVKFLSGTSPHGTNQHSPQVGPTATQAMQEFLTRLQVHLSSTCPQIFSEFLLKLIHILSTERGAFQTGQGPLDAQVKLLEFTLEQNFEVVSVSTISAVIESVTFLVHHYITCSDKVMSRSGSDSSVGARACFGGLFANLIRPGDAKAVCGEMTRDQLMFDLLKLVNILVQLPLSGNREYSARVSVTTNTTDSVSDEEKVSGGKDGNGSSTSVQGSPAYVADLVLANQQIMSQILSALGLCNSSAMAMIIGASGLHLTKHENFHGGLDAISVGDGLFTILTTLSKKASTVHMMLQPILTYMACGYMGRQGSLATCQLSEPLLWFILRVLDTSDALKAFHDMGGVQLICNNMVTSTRAIVNTARSMVSTIMKFLDSGPNKAVDSTLKTRILASEPDNAEGIHNFAPLGTITSSSPTAQPAEVLLQATPPHRRARSAAWSYIFLPEEAWCDLTIHLPAAVLLKEIHIQPHLASLATCPSSVSVEVSADGVNMLPLSTPVVTSGLTYIKIQLVKAEVASAVCLRLHRPRDASTLGLSQIKLLGLTAFGTTSSATVNNPFLPSEDQVSKTSIGWLRLLHHCLTHISDLEGMMASAAAPTANLLQTCAALLMSPYCGMHSPNIEVVLVKIGLQSTRIGLKLIDILLRNCAASGSDPTDLNSPLLFGRLNGLSSDSTIDILYQLGTTQDPGTKDRIQALLKWVSDSARVAAMKRSGRMNYMCPNSSTVEYGLLMPSPSHLHCVAAILWHSYELLVEYDLPALLDQELFELLFNWSMSLPCNMVLKKAVDSLLCSMCHVHPNYFSLLMGWMGITPPPVQCHHRLSMTDDSKKQDLSSSLTDDSKNAQAPLALTESHLATLASSSQSPEAIKQLLDSGLPSLLVRSLASFCFSHISSSESIAQSIDISQDKLRRHHVPQQCNKMPITADLVAPILRFLTEVGNSHIMKDWLGGSEVNPLWTALLFLLCHSGSTSGSHNLGAQQTSARSASLSSAATTGLTTQQRTAIENATVAFFLQCISCHPNNQKLMAQVLCELFQTSPQRGNLPTSGNISGFIRRLFLQLMLEDEKVTMFLQSPCPLYKGRINATSHVIQHPMYGAGHKFRTLHLPVSTTLSDVLDRVSDTPSITAKLISEQKDDKEKKNHEEKEKVKAENGFQDNYSVVVASGLKSQSKRAVSATPPRPPSRRGRTIPDKIGSTSGAEAANKIITVPVFHLFHKLLAGQPLPAEMTLAQLLTLLYDRKLPQGYRSIDLTVKLGSRVITDPSLSKTDSYKRLHPEKDHGDLLASCPEDEALTPGDECMDGILDESLLETCPIQSPLQVFAGMGGLALIAERLPMLYPEVIQQVSAPVVTSTTQEKPKDSDQFEWVTIEQSGELVYEAPETVAAEPPPIKSAVQTMSPIPAHSLAAFGLFLRLPGYAEVLLKERKHAQCLLRLVLGVTDDGEGSHILQSPSANVLPTLPFHVLRSLFSTTPLTTDDGVLLRRMALEIGALHLILVCLSALSHHSPRVPNSSVNQTEPQVSSSHNPTSTEEQQLYWAKGTGFGTGSTASGWDVEQALTKQRLEEEHVTCLLQVLASYINPVSSAVNGEAQSSHETRGQNSNALPSVLLELLSQSCLIPAMSSYLRNDSVLDMARHVPLYRALLELLRAIASCAAMVPLLLPLSTENGEEEEEQSECQTSVGTLLAKMKTCVDTYTNRLRSKRENVKTGVKPDASDQEPEGLTLLVPDIQKTAEIVYAATTSLRQANQEKKLGEYSKKAAMKPKPLSVLKSLEEKYVAVMKKLQFDTFEMVSEDEDGKLGFKVNYHYMSQVKNANDANSAARARRLAQEAVTLSTSLPLSSSSSVFVRCDEERLDIMKVLITGPADTPYANGCFEFDVYFPQDYPSSPPLVNLETTGGHSVRFNPNLYNDGKVCLSILNTWHGRPEEKWNPQTSSFLQVLVSVQSLILVAEPYFNEPGYERSRGTPSGTQSSREYDGNIRQATVKWAMLEQIRNPSPCFKEVIHKHFYLKRVEIMAQCEEWIADIQQYSSDKRVGRTMSHHAAALKRHTAQLREELLKLPCPEGLDPDTDDAPEVCRATTGAEETLMHDQVKPSSSKELPSDFQL
種類予測
Score>80(red) has high confidence and is suggested to be used for WB detection. *The prediction model is mainly based on the alignment of immunogen sequences, the results are for reference only, not as the basis of quality assurance.
High(score>80) Medium(80>score>50) Low(score<50) No confidence
PTMs - Q9NR09 基板として
Site | PTM Type | Enzyme | Source |
---|---|---|---|
K92 | Ubiquitination | Uniprot | |
K110 | Ubiquitination | Uniprot | |
K116 | Ubiquitination | Uniprot | |
Y132 | Phosphorylation | Uniprot | |
K197 | Ubiquitination | Uniprot | |
K201 | Ubiquitination | Uniprot | |
K212 | Ubiquitination | Uniprot | |
Y301 | Phosphorylation | Uniprot | |
K408 | Ubiquitination | Uniprot | |
K416 | Ubiquitination | Uniprot | |
S449 | Phosphorylation | Uniprot | |
T453 | Phosphorylation | Uniprot | |
S462 | Phosphorylation | Uniprot | |
S464 | Phosphorylation | Uniprot | |
S473 | Phosphorylation | Uniprot | |
S480 | Phosphorylation | Uniprot | |
S482 | Phosphorylation | Uniprot | |
S486 | Phosphorylation | Uniprot | |
S488 | Phosphorylation | Uniprot | |
S547 | Phosphorylation | Uniprot | |
K548 | Ubiquitination | Uniprot | |
S549 | Phosphorylation | Uniprot | |
T552 | Phosphorylation | Uniprot | |
T574 | Phosphorylation | Uniprot | |
Y575 | Phosphorylation | Uniprot | |
S577 | Phosphorylation | Uniprot | |
T580 | Phosphorylation | Uniprot | |
S581 | Phosphorylation | Uniprot | |
S584 | Phosphorylation | Uniprot | |
S585 | Phosphorylation | Uniprot | |
S587 | Phosphorylation | Uniprot | |
S590 | Phosphorylation | Uniprot | |
S620 | Phosphorylation | Uniprot | |
T626 | Phosphorylation | Uniprot | |
Y633 | Phosphorylation | Uniprot | |
S638 | Phosphorylation | Uniprot | |
K644 | Ubiquitination | Uniprot | |
S647 | Phosphorylation | Uniprot | |
K845 | Ubiquitination | Uniprot | |
S999 | Phosphorylation | Uniprot | |
T1035 | Phosphorylation | Uniprot | |
T1076 | Phosphorylation | Uniprot | |
T1123 | Phosphorylation | Uniprot | |
K1128 | Ubiquitination | Uniprot | |
T1204 | Phosphorylation | Uniprot | |
K1210 | Ubiquitination | Uniprot | |
S1248 | Phosphorylation | Uniprot | |
K1250 | Methylation | Uniprot | |
K1250 | Ubiquitination | Uniprot | |
K1255 | Ubiquitination | Uniprot | |
S1258 | Phosphorylation | Uniprot | |
K1265 | Ubiquitination | Uniprot | |
K1277 | Ubiquitination | Uniprot | |
T1281 | Phosphorylation | Uniprot | |
S1282 | Phosphorylation | Uniprot | |
T1284 | Phosphorylation | Uniprot | |
T1302 | Phosphorylation | Uniprot | |
K1380 | Ubiquitination | Uniprot | |
K1643 | Ubiquitination | Uniprot | |
K1648 | Ubiquitination | Uniprot | |
T1710 | Phosphorylation | Uniprot | |
S1717 | Phosphorylation | Uniprot | |
K1857 | Ubiquitination | Uniprot | |
Y1864 | Phosphorylation | Uniprot | |
S1866 | Phosphorylation | Uniprot | |
T1867 | Phosphorylation | Uniprot | |
S2018 | Phosphorylation | Uniprot | |
S2019 | Phosphorylation | Uniprot | |
S2122 | Phosphorylation | Uniprot | |
S2222 | Phosphorylation | Uniprot | |
K2233 | Ubiquitination | Uniprot | |
K2239 | Ubiquitination | Uniprot | |
K2246 | Ubiquitination | Uniprot | |
K2250 | Ubiquitination | Uniprot | |
K2258 | Ubiquitination | Uniprot | |
K2265 | Ubiquitination | Uniprot | |
K2270 | Ubiquitination | Uniprot | |
K2277 | Ubiquitination | Uniprot | |
K2287 | Ubiquitination | Uniprot | |
T2295 | Phosphorylation | Uniprot | |
T2305 | Phosphorylation | Uniprot | |
T2309 | Phosphorylation | Uniprot | |
K2311 | Ubiquitination | Uniprot | |
K2511 | Ubiquitination | Uniprot | |
T2530 | Phosphorylation | Uniprot | |
K2907 | Ubiquitination | Uniprot | |
S2955 | Phosphorylation | Uniprot | |
K3139 | Ubiquitination | Uniprot | |
S3143 | Phosphorylation | Uniprot | |
K3146 | Ubiquitination | Uniprot | |
S3289 | Phosphorylation | Uniprot | |
K3395 | Ubiquitination | Uniprot | |
S3578 | Phosphorylation | Uniprot | |
K3585 | Ubiquitination | Uniprot | |
S3591 | Phosphorylation | Uniprot | |
K3597 | Ubiquitination | Uniprot | |
S3629 | Phosphorylation | Uniprot | |
S3633 | Phosphorylation | Uniprot | |
S3649 | Phosphorylation | Uniprot | |
S3660 | Phosphorylation | Uniprot | |
K3675 | Methylation | Uniprot | |
T3679 | Phosphorylation | Uniprot | |
S3742 | Phosphorylation | Uniprot | |
K3834 | Ubiquitination | Uniprot | |
K3854 | Ubiquitination | Uniprot | |
K3882 | Ubiquitination | Uniprot | |
Y3912 | Phosphorylation | Uniprot | |
S3913 | Phosphorylation | Uniprot | |
T3931 | Phosphorylation | Uniprot | |
S3937 | Phosphorylation | Uniprot | |
K3946 | Ubiquitination | Uniprot | |
S4010 | Phosphorylation | Uniprot | |
S4019 | Phosphorylation | Uniprot | |
K4020 | Ubiquitination | Uniprot | |
T4021 | Phosphorylation | Uniprot | |
S4023 | Phosphorylation | Uniprot | |
K4110 | Ubiquitination | Uniprot | |
Y4130 | Phosphorylation | Uniprot | |
K4176 | Ubiquitination | Uniprot | |
T4227 | Phosphorylation | Uniprot | |
Y4288 | Phosphorylation | Uniprot | |
S4299 | Phosphorylation | Uniprot | |
K4312 | Ubiquitination | Uniprot | |
C4443 | S-Nitrosylation | Uniprot | |
K4463 | Ubiquitination | Uniprot | |
Y4489 | Phosphorylation | Uniprot | |
K4522 | Acetylation | Uniprot | |
S4523 | Phosphorylation | Uniprot | |
K4527 | Methylation | Uniprot | |
Y4528 | Phosphorylation | Uniprot | |
K4534 | Methylation | Uniprot | |
S4561 | Phosphorylation | Uniprot | |
S4571 | Phosphorylation | Uniprot | |
S4714 | Phosphorylation | Uniprot | |
T4717 | Phosphorylation | Uniprot | |
S4724 | Phosphorylation | Uniprot | |
K4810 | Ubiquitination | Uniprot |
研究背景
Anti-apoptotic protein which can regulate cell death by controlling caspases and by acting as an E3 ubiquitin-protein ligase. Has an unusual ubiquitin conjugation system in that it could combine in a single polypeptide, ubiquitin conjugating (E2) with ubiquitin ligase (E3) activity, forming a chimeric E2/E3 ubiquitin ligase. Its tragets include CASP9 and DIABLO/SMAC. Acts as an inhibitor of CASP3, CASP7 and CASP9. Important regulator for the final stages of cytokinesis. Crucial for normal vesicle targeting to the site of abscission, but also for the integrity of the midbody and the midbody ring, and its striking ubiquitin modification.
Ubiquitinated. Ubiquitination is mediated by the RNF41 E3 ligase and leads to proteasomal degradation, impairing inhibition of apoptosis. Deubiquitinated by USP8/UBPY.
Golgi apparatus>trans-Golgi network membrane. Endosome. Cytoplasm>Cytoskeleton>Spindle pole. Cytoplasm>Cytoskeleton>Microtubule organizing center>Centrosome. Midbody>Midbody ring.
Note: Exhibits cell cycle-dependent localization. Concentrates in a pericentriolar compartment in interphase, moves partially to spindle poles in metaphase, and finally localizes to the spindle midzone and the midbody in telophase and during cytokinesis. On the midbody, localizes to the midbody ring, also called Flemming body (PubMed:18329369). In interphase cells, localizes to the trans-Golgi network membrane and endosomes. During cytokinesis, a fraction moves to the midzone where it specifically arrives at the midbody ring. After abscission completion, travels with the midbody remnant into one daughter cell, and remains bound to it until a new midbody ring is formed during the next cell division (PubMed:18329369).
Expressed in brain cancer cells.
Homodimer. Binds the activated, processed forms of CASP3, CASP6, CASP7 and CASP9. Interacts with RNF41, DIABLO/SMAC, HTRA2, KIF23/MKLP1, USP8/UBPY, BIRC5/survivin, MAP2K1/MEK1, RAB8A/RAB8, RAB11A/RAB11, PLK1, EXOC3/SEC6 and EXOC4/SEC8.
The BIR domain is essential for its antiapoptotic function and is important for binding to DIABLO/SMAC and CASP9.
In the C-terminal section; belongs to the ubiquitin-conjugating enzyme family.
研究領域
· Cellular Processes > Cell growth and death > Apoptosis - multiple species. (View pathway)
· Genetic Information Processing > Folding, sorting and degradation > Ubiquitin mediated proteolysis. (View pathway)
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