Anti-RBM10 Antibody (CAB4209)
- SKU:
- CAB4209
- Product type:
- Antibody
- Reactivity:
- Human
- Host Species:
- Rabbit
- Isotype:
- IgG
- Research Area:
- Epigenetics and Nuclear Signaling
Frequently bought together:
Description
抗体名: | Anti-RBM10 Antibody |
抗体コード: | CAB4209 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB |
反応性: | Human |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human RBM10 (NP_005667.2). |
申し込み: | WB |
推奨希釈: | WB 1:500 - 1:2000 |
反応性: | Human |
ポジティブサンプル: | Jurkat, MCF7, LO2, 293T |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 1-180 of human RBM10 (NP_005667.2). |
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: | MEYE RRGG RGDR TGRY GATD RSQD DGGE NRSR DHDY RDMD YRSY PREY GSQE GKHD YDDS SEEQ SAED SYEA SPGS ETQR RRRR RHRH SPTG PPGF PRDG DYRD QDYR TEQG EEEE EEED EEEE EKAS NIVM LRML PQAA TEDD IRGQ LQSH GVQA REVR LMRN KSSG QSRG FAFV EFSH |
遺伝子ID: | 8241 |
Uniprot: | P98175 |
セルラーロケーション: | Nucleus |
計算された分子量: | 94kDa/103kDa |
観察された分子量: | 105kDa |
同義語: | RBM10, DXS8237E, GPATC9, GPATCH9, S1-1, TARPS, ZRANB5 |
バックグラウンド: | This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants. |
UniProt Protein Function: | May be involved in post-transcriptional processing, most probably in mRNA splicing. Binds to RNA homopolymers, with a preference for poly(G) and poly(U) and little for poly(A). |
NCBI Summary: | This gene encodes a nuclear protein that belongs to a family proteins that contain an RNA-binding motif. The encoded protein associates with hnRNP proteins and may be involved in regulating alternative splicing. Defects in this gene are the cause of the X-linked recessive disorder, TARP syndrome. Alternate splicing results in multiple transcript variants.[provided by RefSeq, Mar 2011] |
UniProt Code: | P98175 |
NCBI GenInfo Identifier: | 218512116 |
NCBI Gene ID: | 8241 |
NCBI Accession: | P98175.3 |
UniProt Secondary Accession: | P98175,Q14136, Q5JRR2, Q9BTE4, Q9BTX0, Q9NTB1, C4AM81 |
UniProt Related Accession: | P98175 |
Molecular Weight: | 930 |
NCBI Full Name: | RNA-binding protein 10 |
NCBI Synonym Full Names: | RNA binding motif protein 10 |
NCBI Official Symbol: | RBM10 |
NCBI Official Synonym Symbols: | S1-1; TARPS; GPATC9; ZRANB5; GPATCH9; DXS8237E |
NCBI Protein Information: | RNA-binding protein 10; RNA-binding protein S1-1; g patch domain-containing protein 9 |
UniProt Protein Name: | RNA-binding protein 10 |
UniProt Synonym Protein Names: | G patch domain-containing protein 9; RNA-binding motif protein 10; RNA-binding protein S1-1; S1-1 |
Protein Family: | RNA-binding protein |
UniProt Gene Name: | RBM10 |
UniProt Entry Name: | RBM10_HUMAN |
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