SLC25A42 Rabbit Polyclonal Antibody
CAT#: TA334622
Rabbit Polyclonal Anti-SLC25A42 Antibody
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CNY 5250.00
Cited in 2 publications. |
CNY 3080.00
CNY 300.00
CNY 1430.00
CNY 2900.00
CNY 6650.00
CNY 9998.00
Specifications
Product Data | |
Applications | WB |
Recommend Dilution | WB |
Reactivity | Human |
Host | Rabbit |
Clonality | Polyclonal |
Immunogen | The immunogen for anti-SLC25A42 antibody: synthetic peptide directed towards the N terminal of human SLC25A42. Synthetic peptide located within the following region: GNGVKEGPVRLHEDAEAVLSSSVSSKRDHRQVLSSLLPGALAGALAKTAV |
Isotype | IgG |
Formulation | Liquid. Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose. |
Purification | Affinity Purified |
Conjugation | Unconjugated |
Storage Condition | Store at -20°C as received. |
Predicted Protein Size | 35 kDa |
Gene Name | solute carrier family 25 member 42 |
Database Link | |
Background | SLC25A42 belongs to the SLC25 family of mitochondrial carrier proteins.The exact function of SLC25A42 remains unknown.SLC25A42 belongs to the SLC25 family of mitochondrial carrier proteins (Haitina et al., 2006 [PubMed 16949250]). [supplied by OMIM]. Sequence Note: removed 2 bases from the 5' end that did not align to the reference genome assembly. PRIMARYREFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP 1-3160 BC045598.1 3-3162 |
Synonyms | MGC26694 |
Note | Immunogen Sequence Homology: Rat: 100%; Human: 100%; Mouse: 100%; Pig: 93%; Bovine: 93%; Rabbit: 93%; Guinea pig: 93%; Dog: 92% |
Reference Data | |
Protein Families | Druggable Genome |
Citations (2)
The use of this Antibodies has been cited in the following citations: |
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SLC25A42‐associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion, et al. SLC25A42‐associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion
,null,
JIMD Reports
,PubMed ID 34258143
[SLC25A42]
|
SLC25A42‐associated mitochondrial encephalomyopathy: Report of additional founder cases and functional characterization of a novel deletion
,Aldosary, M;Baselm, S;Abdulrahim, M;Almass, R;Alsagob, M;AlMasseri, Z;Huma, R;AlQuait, L;Al‐Shidi, T;Al‐Obeid, E;AlBakheet, A;Alahideb, B;Alahaidib, L;Qari, A;Taylor, R;Colak, D;AlSayed, M;Kaya, N;,
JIMD Reports
[SLC25A42]
|
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