Anti-WRB Antibody (CAB7000)
- SKU:
- CAB7000
- Product type:
- Antibody
- 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-WRB Antibody |
抗体コード: | CAB7000 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB IHC |
反応性: | Mouse, Rat |
宿主種: | Rabbit |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 30-100 of human WRB (NP_004618.2). |
申し込み: | WB IHC |
推奨希釈: | WB 1:500 - 1:2000 IHC 1:50 - 1:200 |
反応性: | Mouse, Rat |
ポジティブサンプル: | Mouse testis, Mouse skin, Rat lung, Rat brain |
免疫原: | Recombinant fusion protein containing a sequence corresponding to amino acids 30-100 of human WRB (NP_004618.2). |
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: | SFSS FMSR VLQK DAEQ ESQM RAEI QDMK QELS TVNM MDEF ARYA RLER KINK MTDK LKTH VKAR TAQL AKI |
遺伝子ID: | 7485 |
Uniprot: | O00258 |
セルラーロケーション: | Endoplasmic reticulum membrane, Multi-pass membrane protein |
計算された分子量: | 16kDa/19kDa |
観察された分子量: | 25kDa |
同義語: | WRB, CHD5, GET1 |
バックグラウンド: | This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
UniProt Protein Function: | WRB: Receptor for ASNA1/TRC40-mediated insertion of tail- anchored (TA) proteins into the ER membrane. Belongs to the WRB/GET1 family. 2 isoforms of the human protein are produced by alternative splicing. |
UniProt Protein Details: | Protein type:Membrane protein, multi-pass; Membrane protein, integral Chromosomal Location of Human Ortholog: 21q22.3 Cellular Component: endoplasmic reticulum membrane; integral to membrane; nucleus |
NCBI Summary: | This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Apr 2009] |
UniProt Code: | O00258 |
NCBI GenInfo Identifier: | 12643986 |
NCBI Gene ID: | 7485 |
NCBI Accession: | O00258.2 |
UniProt Secondary Accession: | O00258,O60740, A8KAP8, A8MQ44, D3DSH9, |
UniProt Related Accession: | O00258 |
Molecular Weight: | 174 |
NCBI Full Name: | Tail-anchored protein insertion receptor WRB |
NCBI Synonym Full Names: | tryptophan rich basic protein |
NCBI Official Symbol: | WRB |
NCBI Official Synonym Symbols: | CHD5 |
NCBI Protein Information: | tail-anchored protein insertion receptor WRB; tryptophan-rich protein; tryptophan-rich basic protein; congenital heart disease 5 protein |
UniProt Protein Name: | Tail-anchored protein insertion receptor WRB |
UniProt Synonym Protein Names: | Congenital heart disease 5 protein; Tryptophan-rich basic protein; WRB |
Protein Family: | Tail-anchored protein insertion receptor |
UniProt Gene Name: | WRB |
UniProt Entry Name: | WRB_HUMAN |
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