BBS7 anticorps (AA 1-270)
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- Antigène Voir toutes BBS7 Anticorps
- BBS7 (Bardet-Biedl Syndrome 7 (BBS7))
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Épitope
- AA 1-270
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp BBS7 est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (IHC)
- Fonction
- BBS7 Rabbit pAb
- Séquence
- MDLILNRMDY LQVGVTSQKT MKLIPASRHR ATQKVVIGDH DGVVMCFGMK KGEAAAVFKT LPGPKIARLE LGGVINTPQE KIFIAAASEI RGFTKRGKQF LSFETNLTES IKAMHISGSD LFLSASYIYN HYCDCKDQHY YLSGDKINDV ICLPVERLSR ITPVLACQDR VLRVLQGSDV MYAVEVPGPP TVLALHNGNG GDSGEDLLFG TSDGKLALIQ ITTSKPVRKW EIQNEKKRGG ILCIDSFDIV GDGVKDLLVG RDDGMVEVYS
- Réactivité croisée
- Humain, Souris, Rat
- Attributs du produit
- Polyclonal Antibodies
- Purification
- Affinity purification
- Immunogène
- Recombinant fusion protein containing a sequence corresponding to amino acids 1-270 of human BBS7 (NP_060660.2).
- Isotype
- IgG
- Top Product
- Discover our top product BBS7 Anticorps primaire
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- Indications d'application
- WB,1:500 - 1:2000,IHC,1:50 - 1:100,IF,1:50 - 1:200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- Agent conservateur
- Sodium azide
- Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Avoid freeze / thaw cycles.
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- Antigène
- BBS7 (Bardet-Biedl Syndrome 7 (BBS7))
- Autre désignation
- BBS7 (BBS7 Produits)
- Synonymes
- anticorps BBS7, anticorps bbs2l1, anticorps BBS2L1, anticorps id:ibd5048, anticorps zgc:153772, anticorps 8430406N16Rik, anticorps Bardet-Biedl syndrome 7, anticorps bardet-biedl syndrome 7, anticorps Bardet-Biedl syndrome 7 L homeolog, anticorps Bardet-Biedl syndrome 7 (human), anticorps BBS7, anticorps bbs7, anticorps MICPUN_100192, anticorps MICPUCDRAFT_16331, anticorps bbs7.L, anticorps Bbs7
- Sujet
- This gene encodes one of eight proteins that form the BBSome complex containing BBS1, BBS2, BBS4, BBS5, BBS7, BBS8, BBS9 and BBIP10. The BBSome complex is believed to recruit Rab8(GTP) to the primary cilium and promote ciliogenesis. The BBSome complex assembly is mediated by a complex composed of three chaperonin-like BBS proteins (BBS6, BBS10, and BBS12) and CCT/TRiC family chaperonins. Mutations in this gene are implicated in Bardet-Biedl syndrome, a genetic disorder whose symptoms include obesity, retinal degeneration, polydactyly and nephropathy, however, mutations in this gene and the BBS8 gene are thought to play a minor role and mutations in chaperonin-like BBS genes are found to be a major contributor to disease development in a multiethnic Bardet-Biedl syndrome patient population. Two transcript variants encoding distinct isoforms have been identified for this gene.[provided by RefSeq, Oct 2014],BBS2L1,BBS7,Cancer,Cell Biology & Developmental Biology,Cell Cycle,Centrosome,Endocrine & Metabolism,Neuroscience,BBS7
- Poids moléculaire
- 75kDa/80kDa
- ID gène
- 55212
- UniProt
- Q8IWZ6
- Pathways
- Signalisation Hedgehog
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