Anti-PNKD Antibody (CAB8203)
- SKU:
- CAB8203
- Product type:
- Antibody
- Application:
- WB
- Application:
- IF
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Epigenetics and Nuclear Signaling
Frequently bought together:
Description
抗体名: | PNKD Rabbit Polyclonal Antibody |
抗体コード: | CAB8203 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IF |
反応性: | Human, Mouse |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-270 of human PNKD (NP_056303.3). |
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 |
ポジティブサンプル: | A-549, 22Rv1, THP-1, Mouse brain, Mouse kidney |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-270 of human PNKD (NP_056303.3). |
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: | MAAV VAAT ALKG RGAR NARV LRGI LAGA TANK ASHN RTRA LQSH SSPE GKEE PEPL SPEL EYIP RKRG KNPM KAVG LAWY SLYT RTWL GYLF YRQQ LRRA RNRY PKGH SKTQ PRLF NGVK VLPI PVLS DNYS YLII DTQA QLAV AVDP SDPR AVQA SIEK EGVT LVAI LCTH KHWD HSGG NRDL SRRH RDCR VYGS PQDG IPYL THPL CHQD VVSV GRLQ IRAL ATPG HTQG HLVY LLDG EPYK GPSC LFSG DLLF LSGC GRTF EGNA ET |
遺伝子ID: | 25953 |
Uniprot: | Q8N490 |
セルラーロケーション: | Cytoplasm, Membrane, Mitochondrion, Nucleus, Peripheral membrane protein |
計算された分子量: | 15kDa/36kDa/40kDa/42kDa |
観察された分子量: | 43kDa |
同義語: | PNKD, BRP17, DYT8, FKSG19, FPD1, KIPP1184, MR-1, MR1, PDC, PKND1, TAHCCP2 |
バックグラウンド: | This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. |
UniProt Protein Function: | Probable hydrolase that plays an aggravative role in the development of cardiac hypertrophy via activation of the NF-kappa-B signaling pathway. |
NCBI Summary: | This gene is thought to play a role in the regulation of myofibrillogenesis. Mutations in this gene have been associated with the movement disorder paroxysmal non-kinesigenic dyskinesia. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010] |
UniProt Code: | Q8N490 |
NCBI GenInfo Identifier: | 158563846 |
NCBI Gene ID: | 25953 |
NCBI Accession: | Q8N490.2 |
UniProt Secondary Accession: | Q8N490,Q96A48, Q9BU26, Q9NSX4, Q9ULN6, Q9Y4T1, A8K1F2 |
UniProt Related Accession: | Q8N490 |
Molecular Weight: | 36,849 Da |
NCBI Full Name: | Probable hydrolase PNKD |
NCBI Synonym Full Names: | paroxysmal nonkinesigenic dyskinesia |
NCBI Official Symbol: | PNKD |
NCBI Official Synonym Symbols: | MR1; PDC; DYT8; FPD1; MR-1; BRP17; PKND1; FKSG19; TAHCCP2; KIPP1184 |
NCBI Protein Information: | probable hydrolase PNKD |
UniProt Protein Name: | Probable hydrolase PNKD |
UniProt Synonym Protein Names: | Myofibrillogenesis regulator 1; MR-1; Paroxysmal nonkinesiogenic dyskinesia protein; Trans-activated by hepatitis C virus core protein 2 |
Protein Family: | Probable hydrolase |
UniProt Gene Name: | PNKD |
UniProt Entry Name: | PNKD_HUMAN |
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