Overview:
| Product Name | CXCR4 Antibody | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Description | Rabbit Anti-Human CXCR4 Polyclonal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Species Reactivity | Human, Mouse, Rat | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Applications | WB, IHC | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Antibody Dilution | WB (1:2000), IHC (1:200); optimal dilutions for assays should be determined by the user. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Host Species | Rabbit | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Immunogen Species | Human | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Immunogen | A synthesized peptide derived from human CXCR4 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Conjugates |
Alkaline Phosphatase, APC, ATTO 390, ATTO 488, ATTO 565, ATTO 594, ATTO 633, ATTO 655, ATTO 680, ATTO 700, Biotin, FITC, HRP, PE/ATTO 594, PerCP, RPE, Streptavidin, Unconjugated
StreptavidinProperties:
Streptavidin Datasheet Biotin | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| R-PE (R-Phycoerythrin) | ||
Overview:
R-PE Datasheet | ![]() | Optical Properties: λex = 565 nm λem = 575 nm εmax = 2.0×106 Φf = 0.84 Brightness = 1.68 x 103 Laser = 488 to 561 nm Filter set = TRITC |
Properties
| Storage Buffer | PBS pH 7.4, 50% glycerol, 150mM NaCl, 0.02% sodium azide |
| Storage Temperature | -20ºC |
| Shipping Temperature | Blue Ice or 4ºC |
| Purification | Affinity Purified |
| Clonality | Polyclonal |
| Isotype | IgG |
| Specificity | Detects ~45kDa, endogenous levels of total CXCR4. |
| Cite This Product | StressMarq Biosciences Cat# SPC-1293, RRID: AB_2713079 |
| Certificate of Analysis | A 1:1000 dilution of SPC-1293 was sufficient for detection of CXCR4 in 10 µg of K562 cell lysates by ECL immunoblot analysis using Goat Anti-Rabbit IgG:HRP as the secondary antibody. |
Biological Description
| Alternative Names | C-X-C chemokine receptor type 4 Antibody, CD184 Antibody, CD184 antigen Antibody, Chemokine (C X C motif) receptor 4 Antibody, Chemokine CXC Motif Receptor 4 Antibody, CXC-R4 Antibody, CXCR-4 Antibody, CXCR4 Antibody, CXCR4_HUMAN Antibody, D2S201E Antibody, FB22 Antibody, Fusin Antibody, HM89 Antibody, HSY3RR Antibody, LAP 3 Antibody, LAP3 Antibody, LCR1 Antibody, LESTR Antibody, Leukocyte derived seven transmembrane domain receptor Antibody, Leukocyte-derived seven transmembrane domain receptor Antibody, Lipopolysaccharide associated protein 3 Antibody, Neuropeptide Y receptor Y3 Antibody, NPY3R Antibody, NPYR Antibody, NPYRL Antibody, NPYY3 Antibody, NPYY3R Antibody, Probable G protein coupled receptor lcr1 homolog Antibody, SDF 1 receptor Antibody, SDF-1 receptor Antibody, SEVEN-TRANSMEMBRANE-SEGMENT RECEPTOR Antibody, Stromal cell derived factor 1 receptor Antibody, Stromal cell-derived factor 1 receptor Antibody, WHIM Antibody |
| Research Areas | Cancer, Neuroscience |
| Cellular Localization | Cell Junction, Cell membrane, Early endosome, Late Endosome, Lysosome |
| Accession Number | NP_003458.1 |
| Gene ID | 7852 |
| Swiss Prot | P61073 |
| Scientific Background | C-X-C chemokine receptor type 4 (CXCR-4) is a protein that in humans is encoded by the CXCR4 gene, also known as fusin or CD184 (cluster of differentiation 184). Chemokines and their receptors direct migration of distinct leukocyte subsets to sites of inflammation and to their specific niches in lymphoid organs. Virtually all T cell chemoattractants selectively attract memory/activated T cells. C-X-C chemokine receptor type 4 is involved in haematopoiesis and in cardiac ventricular septum formation. Plays also an essential role in vascularization of the gastrointestinal tract, probably by regulating vascular branching and/or remodeling processes in endothelial cells. It has been associated with WHIM syndrome. WHIM like mutations in CXCR4 were recently identified in patients with Waldenstrom's macroglobulinemia, a B-cell malignancy. |
| References |
1. Moriuchi M. et al. (1997) Journal of Immunology 159 (9): 4322–9. 2. Caruz A. et al. (1998) FEBS Letters 426 (2): 271–8. 3. Balabanian K. et al. (2008) The Journal of Clinical Investigation 118 (3): 1074–84. 4. Hunter Z.R. et al. (2014) Blood 123 (11): 1637–46. |
Product Images
Western blot analysis of Human K562 cell lysates showing detection of ~39kDa CXCR4 protein using Rabbit Anti-CXCR4 Polyclonal Antibody (SPC-1293). Lane 1: Human K562 cell lysate treated with the immunizing peptide. Lane 2: Human K562 cell lysate. Primary Antibody: Rabbit Anti-CXCR4 Polyclonal Antibody (SPC-1293) at 1:1000. Predicted/Observed Size: ~39kDa.
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| ATTO 594 | ||
Overview:
ATTO 594 Datasheet | ![]() | Optical Properties: λex = 601 nm λem = 627 nm εmax = 1.2×105 Φf = 0.85 τfl = 3.5 ns Brightness = 102 Laser = 594 nm Filter set = Texas Red® |
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② 应取pH8.0,这样可使核苷酸带较多负电荷,利于吸附于阴离子交换树脂柱。虽然pH 11.4时核苷酸带有更多的负电荷,但pH过高对分离不利。
③ 当不考虑树脂的非极性吸附时,根据核苷酸负电荷的多少来决定洗脱速度,则洗脱顺序为CMP>AMP> GMP > UMP,但实际上核苷酸和聚苯乙烯阴离子交换树脂之间存在着非极性吸附,嘌呤碱基的非极性吸附是嘧啶碱基的3倍。静电吸附与非极性吸附共同作用的结果使洗脱顺序为:CMP> AMP > UMP >GMP。
1. Buffer中离子浓度过大,甘氨酸或者Tris碱有可能疏忽多加了
2.没有加相应浓度的SDS
3.电泳周围温度高,也是一个原因
我使用的是1%琼脂糖凝胶,电泳缓冲液为0.5×TBE。
请问各位大虾,在不影响实验结果的前提下,这样的含EB的电泳缓冲液可以反复使用多少次?
谢谢^_^
500ml
2。阴极缓冲液 ( 10 × ) :将 60.55g Tris ,89.58g Tricine 及 5g SDS 溶于400ml 蒸馏水中,加水至终体积为500ml
使用时稀释至1×的缓冲液,电泳槽内槽加入阴极电泳缓冲液,外槽加入阳极电泳缓冲液。形成Trcine-SDS-PAGE电泳系统。
如果你是制胶或者做电泳缓冲液的话,不用灭菌。
Tris-Glycine/SDS;
MOPS/SDS;
Bis-Glycine/SDS等不同的缓冲液、预混液等。
不知道这几种缓冲液有什么异同呢?
比如如果是Invitrogen的预制胶-预混液电泳系统,每种预制胶有适配缓冲液,但是如果用其他的缓冲液似乎也可以得到不错的结果,那么是否说明电泳缓冲液只要满足了缓冲ph范围,其他的不是特别重要呢?
此外,附加提问是,PVDF膜在转膜的时候,转膜缓冲液中不需要加入甲醇,那么是加入甲醇转膜效果好还是不加好呢?
谢谢!















