Anti-WDR81 Antibody (CAB12780)
- SKU:
- CAB12780
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
抗体名: | Anti-WDR81 Antibody |
抗体コード: | CAB12780 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IF |
反応性: | Human, Mouse, Rat |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 360-600 of human WDR81 (NP_689561.2). |
申し込み: | WB IF |
推奨希釈: | WB 1:500 - 1:2000 IF 1:50 - 1:200 |
反応性: | Human, Mouse, Rat |
ポジティブサンプル: | Mouse brain |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 360-600 of human WDR81 (NP_689561.2). |
精製方法: | Affinity purification |
ストレージバッファ: | Store at -20'C. Avoid freeze / thaw cycles. Buffer: PBS with 0.02% sodium azide, 50% glycerol, pH7.3. |
アイソタイプ: | IgG |
順序: | RIGQ EMVQ QHLS EPVA TFFQ VFSQ LHEL RQQD LKLD PAGR GEGQ LPQV VFSD GQQR PVDP ALLD ELQK VFTL EMAY TIYV PFSC LLGD IIRK IIPN HELV GELA ALYL ESIS PSSR NPAS VEPT MPGT GPEW DPHG GGCP QDDG HSGT FGSV LVGN RIQI PNDS RPEN PGPL GPIS GVGG GGLG SGSD DNAL KQEL PRSV HGLS GNWL AYWQ YEIG VSQQ DAHF HFHQ IRLQ SFPG HSGA V |
遺伝子ID: | 124997 |
Uniprot: | Q562E7 |
セルラーロケーション: | Mitochondrion |
計算された分子量: | 74kDa/77kDa/79kDa/95kDa/197kDa/211kDa |
観察された分子量: | 260kDa |
同義語: | WDR81, CAMRQ2, PPP1R166, SORF-2 |
バックグラウンド: | This gene encodes a multi-domain transmembrane protein, which is predominantly expressed in the brain. Mutations in this gene are associated with autosomal recessive cerebellar ataxia, mental retardation, and dysequilibrium syndrome-2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
UniProt Protein Function: | WDR81: 2 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Unknown function Chromosomal Location of Human Ortholog: 17p13.3 Disease: Cerebellar Ataxia, Mental Retardation, And Dysequilibrium Syndrome 2 |
NCBI Summary: | This gene encodes a multi-domain transmembrane protein, which is predominantly expressed in the brain. Mutations in this gene are associated with autosomal recessive cerebellar ataxia, mental retardation, and dysequilibrium syndrome-2. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2012] |
UniProt Code: | Q562E7 |
NCBI GenInfo Identifier: | 403314383 |
NCBI Gene ID: | 124997 |
NCBI Accession: | Q562E7.2 |
UniProt Secondary Accession: | Q562E7,Q24JP6, Q8N277, Q8N3F3, Q8TEL1, B3KW16, B3KXU1 B7Z579, E9PHG7, |
UniProt Related Accession: | Q562E7 |
Molecular Weight: | 212kDa |
NCBI Full Name: | WD repeat-containing protein 81 |
NCBI Synonym Full Names: | WD repeat domain 81 |
NCBI Official Symbol: | WDR81 |
NCBI Official Synonym Symbols: | CAMRQ2; SORF-2; PPP1R166 |
NCBI Protein Information: | WD repeat-containing protein 81 |
UniProt Protein Name: | WD repeat-containing protein 81 |
Protein Family: | WD repeat-containing protein |
UniProt Gene Name: | WDR81 |
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