ABIN350114
antibody from antibodies-online
Targeting: SNAP25
bA416N4.2, dJ1068F16.2, RIC-4, RIC4, SEC9, SNAP, SNAP-25
Antibody data
- Antibody Data
- Antigen structure
- References [5]
- Comments [0]
- Validations [0]
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- Product number
- ABIN350114 - Provider product page
- Provider
- antibodies-online
- Proper citation
- Antibodies-Online Cat#ABIN350114, RRID:AB_10785198
- Product name
- anti-Bardet-Biedl Syndrome 4 (BBS4) (C-Term) antibody
- Antibody type
- Polyclonal
- Antigen
- A synthetic peptide from c-terminal region of mouse Aquaporin 7 (AQP7) conjugated to an immunogenic carrier protein was used as the antigen.
- Reactivity
- Human
- Host
- Sheep
- Epitope
- C-Term
- Isotype
- IgG
- Vial size
- 500 μg
- Storage
- Maintain the lyophilised/reconstituted antibodies frozen at -20°C for long term storage and refrigerated at 2-8°C for a shorter term. When reconstituting, glycerol (1:1) may be added for an additional stability.
- Handling
- Avoid freeze and thaw cycles.
Submitted references Testing for triallelism: analysis of six BBS genes in a Bardet-Biedl syndrome family cohort.
The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression.
Cloning and characterization of a splice variant of human Bardet-Biedl syndrome 4 gene (BBS4).
BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance.
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.
Hichri H, Stoetzel C, Laurier V, Caron S, Sigaudy S, Sarda P, Hamel C, Martin-Coignard D, Gilles M, Leheup B, Holder M, Kaplan J, Bitoun P, Lacombe D, Verloes A, Bonneau D, Perrin-Schmitt F, Brandt C, Besancon AF, Mandel JL, Cossée M, Dollfus H
European journal of human genetics : EJHG 2005 May;13(5):607-16
European journal of human genetics : EJHG 2005 May;13(5):607-16
The Bardet-Biedl protein BBS4 targets cargo to the pericentriolar region and is required for microtubule anchoring and cell cycle progression.
Kim JC, Badano JL, Sibold S, Esmail MA, Hill J, Hoskins BE, Leitch CC, Venner K, Ansley SJ, Ross AJ, Leroux MR, Katsanis N, Beales PL
Nature genetics 2004 May;36(5):462-70
Nature genetics 2004 May;36(5):462-70
Cloning and characterization of a splice variant of human Bardet-Biedl syndrome 4 gene (BBS4).
Ye X, Dai J, Fang W, Jin W, Guo Y, Song J, Ji C, Gu S, Xie Y, Mao Y
DNA sequence : the journal of DNA sequencing and mapping 2004 Jun;15(3):213-8
DNA sequence : the journal of DNA sequencing and mapping 2004 Jun;15(3):213-8
BBS4 is a minor contributor to Bardet-Biedl syndrome and may also participate in triallelic inheritance.
Katsanis N, Eichers ER, Ansley SJ, Lewis RA, Kayserili H, Hoskins BE, Scambler PJ, Beales PL, Lupski JR
American journal of human genetics 2002 Jul;71(1):22-9
American journal of human genetics 2002 Jul;71(1):22-9
Identification of the gene that, when mutated, causes the human obesity syndrome BBS4.
Mykytyn K, Braun T, Carmi R, Haider NB, Searby CC, Shastri M, Beck G, Wright AF, Iannaccone A, Elbedour K, Riise R, Baldi A, Raas-Rothschild A, Gorman SW, Duhl DM, Jacobson SG, Casavant T, Stone EM, Sheffield VC
Nature genetics 2001 Jun;28(2):188-91
Nature genetics 2001 Jun;28(2):188-91
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