Anti-SLC52A3 Antibody (CAB15935)
- SKU:
- CAB15935
- Product type:
- Antibody
- Reactivity:
- Mouse
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Signal Transduction
Frequently bought together:
Description
抗体名: | Anti-SLC52A3 Antibody |
抗体コード: | CAB15935 |
抗体サイズ: | 20uL, 50uL, 100uL |
申し込み: | WB |
反応性: | Mouse |
宿主種: | Rabbit |
免疫原: | A synthetic peptide corresponding to a sequence within amino acids 200-300 of human SLC52A3 (NP_212134.3). |
申し込み: | WB |
推奨希釈: | WB 1:500 - 1:2000 |
反応性: | Mouse |
ポジティブサンプル: | Mouse kidney |
免疫原: | A synthetic peptide corresponding to a sequence within amino acids 200-300 of human SLC52A3 (NP_212134.3). |
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: | PGME APLS HLES RYLP AHFS PLVF FLLL SIMM ACCL VAFF VLQR QPRC WEAS VEDL LNDQ VTLH SIRP REEN DLGP AGTV DSSQ GQGY LEEK AAPC CPAH L |
遺伝子ID: | 113278 |
Uniprot: | Q9NQ40 |
セルラーロケーション: | Apical cell membrane, Multi-pass membrane protein |
計算された分子量: | 45kDa/50kDa |
観察された分子量: | 51kDa |
同義語: | SLC52A3, BVVLS, BVVLS1, C20orf54, RFT2, RFVT3, bA371L19.1, hRFT2 |
バックグラウンド: | This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. |
UniProt Protein Function: | Transporter for riboflavin, which must be obtained as a nutrient via intestinal absorption. Riboflavin transport is Na+-independent at low pH but significantly reduced by Na+ depletion under neutral pH conditions. Activity is strongly inhibited by riboflavin analogs, such as lumiflavin, flavin mononucleotide (FMN), flavin adenine dinucleotide (FAD), by methylene blue, and to a lesser extent by amiloride. |
NCBI Summary: | This gene encodes a riboflavin transporter protein that is strongly expressed in the intestine and likely plays a role in intestinal absorption of riboflavin. The protein is predicted to have eleven transmembrane domains and a cell surface localization signal in the C-terminus. Mutations at this locus have been associated with Brown-Vialetto-Van Laere syndrome and Fazio-Londe disease. [provided by RefSeq, Mar 2012] |
UniProt Code: | Q9NQ40 |
NCBI GenInfo Identifier: | 156564359 |
NCBI Gene ID: | 113278 |
NCBI Accession: | NP_212134.3 |
UniProt Secondary Accession: | Q9NQ40,Q5W1A0, Q5W1A1, Q8NCL7, Q96GD5, A8K6P1, |
UniProt Related Accession: | Q9NQ40 |
Molecular Weight: | 45,043 Da |
NCBI Full Name: | solute carrier family 52, riboflavin transporter, member 3 |
NCBI Synonym Full Names: | solute carrier family 52 member 3 |
NCBI Official Symbol: | SLC52A3 |
NCBI Official Synonym Symbols: | RFT2; BVVLS; RFVT3; hRFT2; BVVLS1; C20orf54; bA371L19.1 |
NCBI Protein Information: | solute carrier family 52, riboflavin transporter, member 3 |
UniProt Protein Name: | Solute carrier family 52, riboflavin transporter, member 3 |
UniProt Synonym Protein Names: | Riboflavin transporter 2; hRFT2 |
Protein Family: | Riboflavin transporter |
UniProt Gene Name: | SLC52A3 |
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